help button home button Am J Pathol ASIP WHAT IS IT?
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wu, L.
Right arrow Articles by Mustoe, T. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wu, L.
Right arrow Articles by Mustoe, T. A.
(American Journal of Pathology. 1999;154:301-309.)
© 1999 American Society for Investigative Pathology

Animal Model

Transforming Growth Factor-ß1 Fails to Stimulate Wound Healing and Impairs Its Signal Transduction in an Aged Ischemic Ulcer Model

Importance of Oxygen and Age

Liancun Wu* , Yu-Ping Xia* , Sanford I. Roth{dagger} , Elliott Gruskin{ddagger} and Thomas A. Mustoe*

From the Departments of Surgery* and Pathology{dagger} Northwestern University Medical School, Chicago, Illinois, and the Department of Biotechnology,{ddagger} United States Surgical Corp., North Haven, Connecticut


   Abstract
Top
 Abstract
Introduction
 Materials and Methods
 Results
 Discussion
 References
 
Clinical trials of exogenous growth factors in treating chronic wounds have been less successful than expected. One possible explanation is that most studies used animal models of acute wounds in young animals, whereas most chronic wounds occur in elderly patients with tissue ischemia. We described an animal model of age- and ischemia-impaired wound healing and analyzed the wound-healing response as well as the transforming growth factor (TGF)-ß1 effect in this model. Rabbits of increasing ages were made ischemic in the ear where dermal ulcers were created. Histological analysis showed that epithelium ingrowth and granulation tissue deposition were significantly impaired with increased age under ischemia. TGF-ß1 stimulated wound repair under both ischemic and non-ischemic conditions in young animals, although it showed no statistical difference in aged animals. Procollagen mRNA expression decreased under ischemic conditions and with aging. Neither TGF-ß1 nor procollagen {alpha}1(I) mRNA expression increased in response to TGF-ß1 treatment under ischemia in aged animals. Therefore, the wound-healing process is impaired additively by aging and ischemia. The lack of a wound-healing response to TGF-ß1 in aged ischemic wounds may play a role in the chronic wounds.


   Introduction
Top
 Abstract
 Introduction
Materials and Methods
 Results
 Discussion
 References
 
Many growth factors tested in animal models appear to be promising therapeutic agents promoting wound healing.1 However, clinical trials of growth factors on treating chronic wounds have been less encouraging.2,3 We reasoned that preclinical studies using young animals may not be suitable for predicting growth factor effect on human chronic wounds, which are primarily a problem of aged patients who have local tissue hypoxia. Previously, most preclinical studies have been done on acute wounds in healthy young animals.1,4 Impaired wound-healing models that have been used in many previous studies include young animals with the impaired conditions produced by injecting glucocorticoids, treating with radiation, or decreasing the blood supply to the wound.5-9 Some preclinical studies have examined age effects on wound healing, but truly aged animals (defined as those at the age when one-half of the studied population has died due to natural causes) under the condition of tissue ischemia have not been studied.5,10-12 However, most chronic wounds occur in aged patients with varying degrees of local tissue ischemia secondary to scarring, fibrin cuffing, edema and increased venous pressure in venous stasis, pressure in pressure ulcers, small artery disease, and edema in diabetic ulcers.2,13-15 Therefore, the questions are whether some of the growth factors are less effective in promoting wound healing of aged ischemic animals and whether those altered effects are due to altered gene expression and signal transduction resulting from aging and ischemia.

In general, wounds heal more slowly in healthy elderly human and animals.16-19 Studies suggest that aging is accompanied by altered inflammatory response,20,21 decreased fibroblast proliferation,22 delayed angiogenesis,23 reduced deposition of specific extracellular matrix components,24,25 and slower re-epithelialization.18 However, the effect of tissue ischemia, a common denominator of a number of other disease processes, such as stroke, myocardial infarction and ischemia reperfusion injuries that have a high incidence in the elderly population, has not been studied in aged systems. As the aged population grows, wound healing under impaired conditions secondary to ischemia will increase patient morbidity and mortality after surgery or tissue injury. Clinicians have observed that aged healthy patients can have surgery and heal with few complications.26 However, aged patients with the additive conditions that contribute to local wound tissue ischemia tend to have a higher incidence of surgical wound dehiscence and are at higher risk for developing chronic wounds. Thus, we hypothesize that aging and ischemia have an additive effect on wound healing, and growth factor effects in promoting wound healing may be minimized under ischemic conditions.

Transforming growth factor (TGF)-ß1, one of the strongest stimulators of wound healing as shown in preclinical studies,1,5,27-29 has been associated with various stages of tissue repair.27,29 TGF-ß1 has been shown to stimulate wound healing in young, normal, and ischemic animal models29 when applied locally. Systemic administration of TGF-ß1 stimulated wound healing in a middle-aged rat incisional model.5 A study of the reduced healing rate seen in aged human females suggested a possible role of reproductive hormones in wound healing, and analysis showed a significant difference in re-epithelialization with aging.30 In profound wound healing, deficits of age and ischemia are unknown. Aged mouse dermal cells express less TGF-ß1 mRNA in vivo.31 It has also been shown in vitro that TGF-ß1 binding affinity is impaired under hypoxic conditions in young dermal fibroblasts.32 Our experimental data suggest that aging and ischemia may have additive effects on TGF-ß1 mRNA expression. Collagen synthesis and deposition into the wound is essential during wound healing, and TGF-ß1 is the strongest stimulator of collagen synthesis in wound healing.27 Thus, it is very important to study collagen gene expression under different conditions during wound healing and after TGF-ß1 treatment in both young and aged animals. This research will help evaluate the effects of aging and ischemia and the potential benefit of TGF-ß1 treatment in wound healing. It will also help us learn about the signal transduction of growth factors and the potential effect of aging and ischemia on signal transduction at the molecular level.


   Materials and Methods
Top
 Abstract
 Introduction
 Materials and Methods
Results
 Discussion
 References
 
Dermal Ulcer Wound-Healing Model in Aged Rabbits

New Zealand White male rabbits (Hazelton, Norwalk, CT), young adult (6 months, ranging from 5 to 7 months), retired breeder rabbits, middle-aged (30 months, ranging from 29 to 31 months), upper middle-aged (36 months, ranging from 35 to 37 months), and aged (60 months, ranging from 58 to 62.5 months) were acclimated and kept under standard conditions in the Northwestern University Animal Care Center. As the lifespan of retired breeder laboratory rabbits is ~5 years, which is shorter than that of normal laboratory rabbits, this age is comparable to that of humans in their 7th to 8th decades. This study and its surgical procedures have been approved by the Northwestern University Animal Care and Use Committee. The surgical procedures were performed as previously described9,33 after anesthetizing the rabbits with Ketamine (60 mg/kg) and Xylazine (5 mg/kg). Briefly, one of the rabbit ears was made ischemic by dissecting the rostral and central arteries and interrupting the entire dermal circulation, preserving only the major three veins and the smallest caudal artery. Three full-thickness, 6-mm-diameter circular wounds were created extending down to bare cartilage. The contralateral ear vessels were left undisturbed and served as matched non-ischemic controls. All of the wounds were covered with an occlusive polyurethane dressing (Tegaderm, 3M, Minneapolis, MN) for 12 days. The wounds were bisected and analyzed histologically based on a previous study that showed these wounds were minimally contracted.29 Re-epithelialization rate, percentage of full re-epithelialization, and new granulation tissue formation in all matched wounds were measured as previously described.29,33

TGF-ß1 Effects in Aged Dermal Ulcers

Recombinant human (rh)TGF-ß1 (1 µg/wound; Amgen, Thousand Oaks, CA) was topically applied once to the wounds immediately after wounding. TGF-ß1 was also topically applied to the ischemic wounds made in young, middle-aged, and aged rabbit ears. The dose of TGF-ß1 (1 µg/wound) was chosen based on previous studies that demonstrated it was the optimal dose for ischemic wound healing.34 In all rabbits, whether young or aged, the wounds on contralateral ears served as a paired control and were treated with vehicle alone (PBS). The growth factors were purified to homogeneity by conventional techniques and assayed for endotoxin before use. This growth factor has been tested in vitro and in vivo, and no difference in biological effects was found between recombinant and natural growth factor derived from macrophage.35 The rabbit ear ulcers were harvested and evaluated histologically at day 12 after wounding as previously described.5,29,34

Statistical Analysis

All of the wounds were created and harvested in a matched fashion, and the data were collected in the same manner allowing paired analyses with each animal serving as its own control. A paired two-tailed Student's t-test (Epistat program, Epistat Service, Richardson, TX) was used to detect differences between non-ischemic and ischemic wounds in each age group and between TGF-ß1-treated wounds and matched control wounds. Analysis of one-way variance was used to analyze the differences among different age groups in model development and TGF-ß1-treated wounds. The {chi}2 test was used to analyze the differences in the percentage of full re-epithelialization. Multivariate analysis (Epistat program) was used to analyze the relative responsiveness of adult versus young or aged animals.

Competitive Reverse Transcription Polymerase Chain Reaction

The wound granulation tissue in each rabbit was harvested as previously described.36,37 All three wounds from each ear were processed, and the total cellular RNA was extracted with guanidine thiocyanate/phenol-based reagent according to the manufacturer's instructions (TRI Reagent, Cincinnati, OH).38 All reverse transcription (RT) reactions were performed simultaneously using a master mix to eliminate variability of RT efficiency. A total of 5.0 µg of each RNA sample, with acceptable purity (A260/A280 ratio >=1.8) was converted to cDNA using Moloney murine leukemia virus reverse transcriptase and random primers (Gibco BRL, Grand Island, NY).

Specific polymerase chain reaction (PCR) primers for rabbit glyceraldehyde-3-phosphate dehydrogenase (GAPDH), TGF-ß1, and procollagen 1(I) were designed using conserved sequences from published Genbank complete and partial mRNA sequences of various species. Sequence information of all PCR primers used and the reaction conditions are listed in Table 1 . The PCR products were confirmed by subcloning each into TA cloning vectors (TA cloning kit, Invitrogen, San Diego, CA) and sequencing analysis.39,40 Nonhomologous competitive PCR fragments (mimic) were used as an internal standard to measure the desired product.41,42 Mimic was created using a commercial kit (Clontech, Palo Alto, CA). Serial dilution of a known quantity of mimic was co-amplified with a constant amount of the cDNA sample, which resulted in varying band intensities depending on the ratio between the mimic and the cDNA of interest. The reaction products were electrophoresed on 2% agarose gels. Gel photographs were quantified by densitometry imaging (Imaging Densitometer GS-670, Bio Rad, Richmond, CA), and the ratio of gene product to mimic was plotted against the known quantity of the mimic. At a ratio of one, each curve gives the corresponding concentration of gene product cDNA. Competitive PCR reactions designed to compare the experimental condition with the control were run simultaneously to allow relative comparison of the extrapolated ratios. Results were confirmed by repeating experiments within the same RNA extraction and with multiple rabbits.


View this table:
[in this window]
[in a new window]
  		Table 1. Primer Sequences and PCR Cycle Information

 

   Results
Top
 Abstract
 Introduction
 Materials and Methods
 Results
Discussion
 References
 
Histology studies showed depressed wound healing by age and ischemia. Young non-ischemic wounds had the most healing (Figure 1A) , and young ischemic and aged non-ischemic wounds healed to a lesser degree (Figure 1, B and C) . Aged ischemic wounds had severely impaired healing (Figure 1D) , showing essentially no healing on day 12. Quantitative analysis of new granulation tissue deposition showed a moderate and progressive decrease with aging under non-ischemic conditions and a sharp decrease under ischemic conditions in both middle-aged and aged animals (Figure 2) . Multivariate analysis showed that under non-ischemic condition, significant decrease of wound granulation tissue formation was found between age 30- and 6-month-old rabbits (41.7% decrease, P < 0.01) and 60- and 30-month-old rabbits (70.0% decrease, P < 0.05). Under ischemic condition, the decrease was 92.9% (P < 0.01) between 6- and 30-month-old rabbits, and no significant change was detected between 60- and 30-month-old rabbits. Young ischemic wounds showed a 65% decrease in new granulation tissue formation compared with their age-matched non-ischemic controls. Middle-aged and aged rabbits each had a more than 95% decrease compared with their age-matched control wounds (Figure 2) . Histological analysis of hematoxylin and eosin (H&E)-stained wound tissue sections revealed a significant reduction of re-epithelialization by age and ischemia (P < 0.01) (Figure 3) as well. Multivariate analysis showed significant difference in re-epithelialization with aging: in non-ischemic wounds, 57.1% (P < 0.01) decrease between 30- and 6-month-old rabbits and 76.7% (P < 0.01) decrease between 30- and 60-month-old rabbits. In ischemic wounds, an 80% decrease (P < 0.01) was found between 30- and 6-month-old rabbits, and a 100% (P < 0.05) decrease was found between 30- and 60-month-old rabbits.



View larger version (91K):
[in this window]
[in a new window]
  		Figure 1. Day 12 wounds stained by H&E. Full-thickness wounds were created on ischemic (B and D) and non-ischemic (A and C) rabbit ears using a 6-mm biopsy punch. Severe delay of both granulation tissue formation and re-epithelialization were observed in aged (60 months) ischemic wounds (D) compared with aged non-ischemic wounds (C), young (6 months) ischemic (B), and young non-ischemic (A) wounds. Within each age group, ischemia caused delayed wound healing when A versus B and C versus D were compared. The migrating front of epithelial sheet is indicated by arrows, and the initial cutting sites are indicated by arrowheads. Magnification, x40.

 


View larger version (33K):
[in this window]
[in a new window]
  		Figure 2. Effect of aging and ischemia on new granulation tissue formation. Day 12 wounds were harvested from both ischemic and non-ischemic animals of increasing age and stained with H&E, followed by quantification of granulation tissue formation using a calibrated lens reticule under a light microscope (x10). Reduction of granulation tissue formation was observed with increasing donor age and ischemia. The paired Student's t-test was used for statistical analysis.

 


View larger version (25K):
[in this window]
[in a new window]
  		Figure 3. Effect of aging and ischemia on re-epithelialization. Wounds were harvested on day 12 after wounding from both ischemic and non-ischemic rabbit ears. Re-epithelialization was quantified histologically on H&E-stained tissue sections. Significant decreases in the percentage of complete re-epithelialization among different age groups and under ischemia versus non-ischemia were observed. The paired Student's t-test was used for statistical analysis.

 
TGF-ß1 has been found to stimulate wound healing in several models of young animal, including ischemic, diabetic, and radiation-impaired healing.1 In this study, we found that TGF-ß1 stimulated partial healing of non-ischemic wounds of aged animals at day 12 (Figure 4C) , at which time wounds of young animals showed complete epithelialization (Figure 4A) . Under ischemic conditions, TGF-ß1 stimulated wound healing of young rabbits (Figure 4B) , but it failed to promote the healing of aged rabbits (Figure 4D) . Quantitative analysis of the H&E-stained wound section showed that TGF-ß1 stimulated the growth of new granulation tissue to 136% in young animals and 100% in middle-aged animals, compared with the vehicle-treated control (Figure 5) . Epithelialization was increased to 100% in young animals and 200% in middle-aged animals, compared with the vehicle-treated control (Figure 6) . In either case, TGF-ß1 failed to promote wound healing in aged rabbits (Figures 5 and 6) . This is the first animal model showing that an impaired healing wound failed to respond to TGF-ß1.



View larger version (78K):
[in this window]
[in a new window]
  		Figure 4. H&E staining of day 12 TGF-ß1-treated wound (original magnification, x40). Wounds were treated with TGF-ß1 (1 µg/wound) at the time of wounding. Aged ischemic wounds (D) showed the least healing response to TGF-ß1 treatment, as compared with young non-ischemic (A), young ischemic (B), and aged non-ischemic (C) wounds. Note that the two epithelial sheets have confronted each other in TGF-ß1-treated young non-ischemic wounds (A). Within the same age group, the TGF-ß1 effect is impaired by ischemia, when A versus B and C versus D were compared. The migrating front of epithelial sheet is indicated by arrows, and the initial cutting sites are indicated by arrowheads. Magnification, x40.

 


View larger version (38K):
[in this window]
[in a new window]
  		Figure 5. TGF-ß1 fails to stimulate new granulation tissue formation of ischemic wounds from aged animal donors. Ischemic wounds were treated with TGF-ß1 (1 µg/wound) at the time of wounding. Wounds were harvested on day 12 after wounding and evaluated histologically. PBS vehicle-treated wounds were used as the control for each age group. The aged animals (60 months) showed no increase in new granulation tissue formation, in contrast to a 138% increase in young animals (6 months).

 


View larger version (37K):
[in this window]
[in a new window]
  		Figure 6. TGF-ß1 fails to promote re-epithelialization of ischemic wounds from aged animal donors. Ischemic wounds were treated with TGF-ß1 (1 µg/wound) at the time of wounding. Wounds were harvested on day 12 after wounding and evaluated histologically. PBS vehicle-treated wounds were used as controls for each age group. The aged animals (60 months) showed no increase in re-epithelialization in contrast to a 100% increase in young animals (6 months).

 
Expression of TGF-ß1 mRNA was measured by competitive PCR analysis. In young non-ischemic wounds, TGF-ß1 mRNA reaches its peak at approximately day 7. A significant up-regulation was also observed in ischemic wounds (Figure 7A) . Aged rabbits showed a major decline in the level of TGF-ß1 mRNA under both ischemic and non-ischemic conditions compared with the young rabbits. No significant difference was observed between ischemic and non-ischemic wounds of aged rabbits (Figure 7B) . These data indicated that the aged rabbit wounds not only expressed lower levels of TGF-ß1 mRNA but also lost responsiveness to ischemia in up-regulating TGF-ß1 expression as young animals do. The level of type I procollagen was also quantified by competitive PCR analysis. In non-ischemic wounds, young rabbits expressed a peak level of type I collagen at approximately day 7 (Figure 8A) , whereas in aged animals the expression was delayed but was still rising at day 12 (Figure 8B) . Interestingly, ischemia down-regulated procollagen 1(I) expression in both young and aged rabbits (Figure 8, A and B) . As an internal control, GAPDH showed no significant change of expression with aging and ischemia (unpublished observation).



View larger version (11K):
[in this window]
[in a new window]
  		Figure 7. Ischemic effect on endogenous TGF-ß1 mRNA expression. Ischemic wounds of both young and aged animals were harvested at days 3, 7, and 12 after wounding, using age-matched non-ischemic wounds as controls. Total RNAs were extracted, and the level of TGF-ß1 mRNA with the progression of wound healing was quantified by competitive PCR analysis. Ischemia stimulated TGF-ß1 mRNA expression in young (6 months) animal wounds (A). However, no obvious stimulation was observed in aged (60 months) animal wounds (B).

 


View larger version (12K):
[in this window]
[in a new window]
  		Figure 8. Ischemic effect on collagen-{alpha}1(I) mRNA expression. Excisional wounds of 6-mm were generated and left to heal for 12 days before harvest. Total RNAs were extracted for reverse transcription and PCR amplification. Level of collagen-{alpha}1(I) mRNA with the progression of wound healing was quantified by competitive PCR analysis. The level of collagen-{alpha}1(I) mRNA expression decreased in both ischemic wounds from young (6 months, A), and aged (60 months, B) animal donors.

 
When the wounds were treated with TGF-ß1 growth factor, a consistent pattern of muted response to TGF-ß1 treatment was demonstrated in aged animals. Aged ischemic wounds had a minimal response to TGF-ß1 treatment in terms of TGF-ß1 mRNA expression (Figure 9A) and procollagen expression (Figure 9B) . As both TGF-ß1 and collagen synthesis are endpoints of TGF-ß1 stimuli, the data suggested that signal transduction in aged ischemic wounds was severely impaired due to age and low tissue oxygen supply.



View larger version (28K):
[in this window]
[in a new window]
  		Figure 9. Expression of TGF-ß1 and collagen-{alpha}1(I) mRNA in TGF-ß1-treated wounds. Wounds were treated with TGF-ß1 growth factor (1 µg/wound) immediately after wounding. Wounds were harvested at day 12 after wounding, and RNAs were extracted for reverse transcription and PCR. Level of TGF-ß1 and collagen 1(I) mRNA expression were quantified by competitive PCR under aging and ischemic conditions. Both factors of age and ischemia repressed expression of TGF-ß1 mRNA (A) and collagen-{alpha}1(I) mRNA (B) in TGF-ß1-treated wounds.

 

   Discussion
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
References
 
The rabbit ear wound-healing model was developed and used in our laboratory to study the effect of growth factors in wound healing under normal and ischemic conditions.29,34,43 The model allows us to precisely measure the new granulation tissue formation and re-epithelialization in a matched control manner, because the ear cartilage splints the wound with minimal contraction.29 This model is also ideal for harvesting the new granulation tissue for biochemical analysis of factors intrinsic to wound repair.44 The pathogenesis of chronic wounds found in elderly patients (principally venous ulcers, diabetic ulcers, and pressure sores) is multifactorial, but a common factor in most is varying degrees of local wound tissue hypoxia. Previous animal models have failed to consider the possible additive effect of aging and ischemia and thus have significant limitations in fostering understanding of human chronic wounds. In this study, we developed an aged ischemic model using 60-month-old rabbits, which is equivalent to human life of the 7th to 8th decades.37 We observed profound impairment of granulation tissue formation and re-epithelialization under ischemic conditions with aging. Compared with the young non-ischemic model in which complete healing takes approximately 12 to 14 days, the healing in our aged ischemic model takes more than 20 days. Additionally, we have shown that TGF-ß1 failed to promote wound healing in aged ischemic wounds. This is the first time that a wound-healing animal model showed no response to TGF-ß1 treatment. It may explain some of the difficulties of clinical trials of growth factor on human chronic wounds. It is likely that our model will provide a better opportunity for the study of underlying biochemical and pathological mechanisms in chronic wound healing and allow re-evaluation of the vulnerary effect of growth factors under the specified conditions.

Tissue ischemia is known to be one of the most significant factors leading to chronic wounds.45 To examine the effect of tissue oxygenation, we have carefully studied the possible reversal of the wound-healing deficit in ischemic wounds by hyperbaric oxygen.34 It has shown that treatment of ischemic wounds with hyperbaric oxygen partially reversed the wound-healing deficit in both granulation tissue formation and epithelialization compared with the nontreated ischemic control.34 More recent studies indicated that, in addition to its metabolic effects, low oxygen tension induces gene expression of several growth factor genes that are important in promoting wound healing, such as platelet-derived growth factor (PDGF)-BB, vascular endothelial growth factor (VEGF), and TGF-ß1 as is shown in this report and by others.46-48 It was also reported that hypoxia decreases TGF-ß1 receptor binding and synthesis in dermal fibroblasts.32 Presumably, heme-based proteins function as oxygen sensors leading to a series of chemical steps. Increasing evidence suggests that the chemical responses generated from oxygen sensing have signal-transducing effects.49 The identification of hypoxia-inducible factor (HIF) provided a molecular basis for oxygen-induced gene regulation, the expression of which is regulated by cellular oxygen tension.50,51

Aging itself has an overt effect on gene expression55,56 as well as on many aspects of biochemistry that are pertinent to wound healing. In vitro studies with cell culture showed an age-related decline of epidermal growth factor receptor-binding affinity, phosphorylation, and internalization52,53 as well as activation of mitogen-activated protein kinase.54 An in vivo study demonstrated that aged ischemic wounds have a dramatic decrease in PDGF receptors.37 In this study, we found that aged animals responded very differently to added stress compared with young animals. Hypoxia up-regulated the level of TGF-ß1 mRNA in wounds of young animals, although it elicited only a mild response in aged animals. In vitro, we found that aged keratinocytes migrate more slowly in response to hypoxia, whereas young keratinocytes migrate faster under the same condition (Y.-P. Xia, Y. Zhao, A. Chen, R. Galliano, and T. A. Mustoe, manuscript in preparation). It is likely that the regulatory machinery or the signaling pathway involved in stress management deteriorates with age, and therefore the ability of aged cells to survive environmental stress is reduced.

As TGF-ß1 has a broad effect on all phases of wound repair, we examined the TGF-ß1 effect on wound repair in our aged ischemic model. Previous studies have shown that in the inflammatory phase of repair, release of TGF-ß1 from platelets increases chemotaxis of inflammatory cells into the wound site.57,58 During the inflammation and after it has subsided, TGF-ß1 induces both angiogenesis59 and extracellular matrix accumulation,60 which continues through the remodeling phase of repair. Extracellular matrix production results from the effects of TGF-ß1 on fibroblast, which include chemotaxis, proliferation, and induction of the synthesis and release of the matrix proteins. Additionally, TGF-ß1 has an autoactivation function61 ; therefore, binding to its own receptor could stimulate expression of an elevated level of TGF-ß1. Based on these facts, we analyzed the effect of TGF-ß1 on granulation tissue formation, epithelialization, collagen synthesis, and induction of endogenous TGF-ß1 mRNA expression in our animal model. We found that although TGF-ß1 has been shown to stimulate wound healing in several other animal models under both normal and impaired conditions,61 it failed to stimulate wound healing in the aged-ischemic rabbit model as described in this paper. Given the failure of wounds to respond to TGF-ß1 and the depressed levels of downstream signal transduction events in response to TGF-ß1 (autoinduction of TGF-ß1 and collagen synthesis), it is evident that signal transduction for TGF-ß1 is impaired under aged-ischemic conditions, which could be due to depressed TGF-ß1 receptor level, altered kinase activity, or other downstream signaling events.


   Acknowledgements
 
We thank Amgen Corp. for supplying the recombinant human TGF-ß1, Sharon Lang (Department of Urology, Northwestern University Medical School, Chicago, IL) for her histological assistance, and David Connors (U.S. Surgical Corp.) for his assistance in making PCR primers.


   Footnotes
 
Address reprint requests to Dr. Thomas A. Mustoe, 707 N. Fairbanks Street, Suite 811, Division of Plastic Surgery, Chicago, IL 60611.

Supported in part by NIH grant R01 GM 41303 and a grant from U.S. Surgical Corp. (New Haven, CT).

L. Wu and Y.-P. Xia contributed equally to the work presented here.

Accepted for publication October 14, 1998.


   References
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
 References
 

  1. Pierce GF, Mustoe TA: Pharmacologic enhancement of wound healing. Annu Rev Med 1995, 46:467-481[Medline]
  2. Mustoe TA, Cutler NR, Allman RM, Goode PS, Deuel TF, Prause J, Bear M, Serdar CM, Pierce GF: A phase II study to evaluate recombinant platelet-derived growth factor-BB in the treatment of stage 3 and 4 pressure ulcers. Arch Surg 1994, 129:213-219[Abstract]
  3. Richard JL, Parer-Richard C, Daures JP, Clouet S, Vannereau D, Bringer J, Rodier M, Jacob C, Comte-Bardonnet M: Effect of topical basic fibroblast growth factor on the healing of chronic diabetic neuropathic ulcer of the foot: a pilot, randomized, double-blind, placebo-controlled study. Diabetes Care 1995, 18:64-69[Abstract]
  4. Pierce GF, Tarpley JE, Yanagihara D, Mustoe TA, Fox GM, Thomason A: Platelet-derived growth factor (BB homodimer), transforming growth factor-ß1, and basic fibroblast growth factor in dermal wound healing. Am J Pathol 1992, 140:1375-1388[Abstract]
  5. Beck LS, DeGuzman L, Lee WP, Xu Y, Siegel MW, Amento EP: One systemic administration of transforming growth factor-ß1 reverses age or glucocorticoid-impaired wound healing. J Clin Invest 1993, 92:2841-2849
  6. Pierce GF, Mustoe TA, Lingelbach J, Masakowski VR, Gramates P, Deuel TF: Transforming growth factor ß reverses the glucocorticoid induced wound healing deficit in rats and is regulated by platelet derived growth factor in macrophages. Proc Natl Acad Sci USA 1989, 86:2229-2233[Abstract/Free Full Text]
  7. Mustoe TA, Purdy J, Gramates P, Deuel TF, Thomason A, Pierce GF: Reversal of impaired wound healing in irradiated rats by platelet-derived growth factor-BB. Am J Surg 1989, 158:345-350[Medline]
  8. Albertson S, Hummel RP, Breeden M, Greenhalgh DG: PDGF and FGF reverse the healing impairment in protein-malnourished diabetic mice. Surgery 1993, 114:368-374[Medline]
  9. Wu L, Mustoe TA: Effect of ischemia upon growth factor enhancement of incisional wound healing. Surgery 1995, 117:570-576[Medline]
  10. Cohen BJ, Danon D, Roth GS: Wound repair in mice as influenced by age and antimacrophage serum. J Gerontol 1987, 42:295-301[Medline]
  11. Cox DA, Kunz S, Cerletti N, McMaster GK, Burk RR: Wound healing in aged animals: effects of locally applied transforming growth factor beta 2 in different model systems. Steiner R Weisz PB Langer R eds. Angiogenesis: Key Principles-Science-Technology-Medicine. , :pp 287-295 Birkhauser Verlag, Basel, Switzerland,
  12. Danon D, Kowatch MA, Roth GS: Promotion of wound repair in old mice by local injection of macrophages. Proc Natl Acad Sci USA 1989, 86:2018[Abstract/Free Full Text]
  13. Phillips TJ: Chronic cutaneous ulcers: etiology and epidemiology. J Invest Dermatol 1994, 102:38S-41S[Medline]
  14. Falanga V: Chronic wounds: pathophysiologic and experimental considerations. J Invest Dermatol 1993b, 100:721-725[Medline]
  15. Falanga V: Growth factors and chronic wounds: the need to understand the microenvironment. J Invest Dermatol 1992, 19:667-672
  16. Ashcroft GS, Horan MA, Ferguson MW: The effects of aging on cutaneous wound healing in mammals. J Anat 1995, 187:1-26
  17. Herrick SE, Ireland GW, Simon D, McCollum CN, Ferguson MW: Venous ulcer fibroblasts compared with normal fibroblasts show differences in collagen but not fibronectin production under both normal and hypoxic conditions. J Invest Dermatol 1996, 106:187-193[Medline]
  18. Holt DR, Kirk SJ: Effect of age on wound healing in healthy human beings. Surgery 1992, 112:293-298[Medline]
  19. Sussman MD: Aging of connective tissue: physical properties of healing wounds in young and old rats. Am J Physiol 1973, 224:1167-1171[Free Full Text]
  20. Forcher BK, Cecil HC: Some affects of age on the biochemistry of acute inflammation. Gerontologia 1958, 2:174-182
  21. Ashcroft GS, Horan MA, Ferguson MW: Aging alters the inflammatory and endothelial cell adhesion molecule profiles during human cutaneous wound healing. Lab Invest 1998, 78:47-58[Medline]
  22. Bruce SA, Deamond SF: Longitudinal study of in vivo wound repair and in vitro cellular senescence of dermal fibroblasts. Exp Gerontol 1991, 26:17-27[Medline]
  23. Yamura H, Matsuzawa T: Decrease in capillary growth during aging. Exp Gerontol 1980, 15:145-150[Medline]
  24. Ashcroft GS, Horan MA, Ferguson MW: Aging is associated with reduced deposition of specific extracellular matrix components, an upregulation of angiogenesis, and an altered inflammatory response in a murine incisional wound healing model. J Invest Dermatol 1997, 108:430-437[Medline]
  25. Platt D, Ruhl W: An age dependent determination of lysosomal enzyme activities, as well as the measurements of the incorporation of 14-c-proline and 14-c-glucosamine in subcutaneously implanted polyether sponge. Gerontologia 1972, 18:96-112[Medline]
  26. Chick LR, Walton RL, Reus W, Colen L, Sasmor M: Free flaps in the elderly. Plast Reconstr Surg 1992, 90:87-94[Medline]
  27. Mustoe TA, Pierce GF, Thomason A, Gramates P, Sporn MB, Deuel TF: Accelerated healing of incisional wounds in rats induced by transforming growth factor-ß. Science 1987, 237:1333-1335[Abstract/Free Full Text]
  28. Kane CJM, Hebda PA, Mansbridge JN, Hanawalt PC: Direct evidence for spatial and temporal regulation of transforming growth factor beta 1 expression during cutaneous wound healing. J Cell Physiol 1991, 148:157-173[Medline]
  29. Mustoe TA, Pierce GF, Morishima C, Deuel TF: Growth factor-induced acceleration of tissue repair through direct and inductive activities in a rabbit dermal ulcer model. J Clin Invest 1991, 87:694-703
  30. Ashcroft GS, Dodsworth J, van Boxtel E, Tarnuzzer RW, Horan MA, Schultz GS, Ferguson MW: Estrogen accelerates cutaneous wound healing associated with an increase in TGF-beta1 levels. Nature Med 1997, 3:1209-1215[Medline]
  31. Schmid P, Kunz S, Cerletti N, McMaster G, Cox D: Injury-induced expression of TGF-beta 1 mRNA is enhanced by exogenously applied TGF-beta. Biochem Biophys Res Commun 1993, 194:399-406[Medline]
  32. Falanga V, Takagi H, Ceballos PI, Pardes JB: Low oxygen tension decreases receptor binding of peptide growth factors in dermal fibroblast cultures. Exp Cell Res 1994, 213:80-84[Medline]
  33. Ahn B, Mustoe TA: Effects of ischemia on ulcer wound healing: a new model in the rabbit ear. Ann Plast Surg 1990, 24:17-23[Medline]
  34. Zhao LL, Davidson JD, Roth SI, Mustoe TA: Effect of hyperbaric oxygen and growth factors on rabbit ear ischemic ulcers. Arch Surg 1994, 129:1043-1049[Abstract]
  35. Bourdrel L, Lin C-H, Lauren SL, Elmore RH, Sugarman BJ, Hu S, Westcott KR: Recombinant human transforming growth factor-ß1: expression by Chinese hamster ovary cells, isolation, and characterization. Protein Expres Purif 1993, 4:130-140[Medline]
  36. Brucker MJ, Gruskin E, Farrell CL, Siddiqui A, Mustoe TA: Differential expression of platelet-derived growth factor receptor-beta in an aging model of wound repair. Wound Rep Regul 1996, 4:219-223
  37. Wu L, Brucker M, Gruskin E, Roth SI, Mustoe TA: Differential effects of PDGF-BB in accelerating wound healing on aged versus young animals: the impact of tissue hypoxia. Plast Reconstruct Surg 1997, 99:815-822[Medline]
  38. Chomczynski PA: Reagent for the single-step simultaneous isolation of RNA, DNA and proteins from cell and tissue samples. BioTechniques 1993, 15:532-537[Medline]
  39. Byravan S, Foster LM, Phan T, Verity AN, Campagnoni AT: Murine oligodendroglial cells express nerve growth factor. Proc Natl Acad Sci USA 1994, 91:8812-8816[Abstract/Free Full Text]
  40. Taglialatela M, Wible BA, Caporaso R, Brown AM: Specification of pore properties by the carboxyl terminus of inwardly rectifying K+ channels. Science 1994, 264:844-847[Abstract/Free Full Text]
  41. Siebert PD, Larrick JW: PCR MIMICS: competitive DNA fragments for use as internal standards in quantitative PCR. BioTechniques 1993, 14:244-249[Medline]
  42. Siebert PD, Larrick JW: Competitive PCR. Nature 1992, 359:557-558[Medline]
  43. Wu L, Pierce GF, Galiano RD, Mustoe TA: Keratinocyte growth factor induces granulation tissue in ischemic dermal wounds: the importance of epithelial-mesenchymal cell interaction. Arch Surg 1996, 131:660-666[Abstract]
  44. Wu L, Siddiqui A, Morris DE, Cox DA, Roth SI, Mustoe TA: Transforming growth factor ß3 accelerates wound healing, but does not alter scar prominence in a novel animal model: histology and competitive RT-PCR studies. Arch Surg 1997, 132:753-760[Abstract]
  45. Van de Kerkhof PC, Van Bergen B, Spruijt K, Kuiper JP: Age-related changes in wound healing. Clin Exp Dermatol 1994, 19:369-374[Medline]
  46. Kourembanas S, Hannan RL, Faller DV: Oxygen tension regulates the expression of the platelet-derived growth factor-B chain gene in human endothelial cells. J Clin Invest 1990, 86:670-674
  47. Shweiki D, Itin A, Soffer D, Keshet E: Vascular endothelial growth factor induced by hypoxia may mediate hypoxia-initiated angiogenesis. Nature 1992, 359:843-845[Medline]
  48. Falanga V, Martin TA, Takagi H, Kirsner RS, Helfman T, Pardes J, Ochoa MS: Low oxygen tension increases mRNA levels of alpha 1 (I) procollagen in human dermal fibroblasts. J Cell Physiol 1993, 157:408-412[Medline]
  49. Bunn HF, Poyton RO: Oxygen sensing and molecular adaptation to hypoxia. Physiol Rev 1996, 76:839-885[Abstract/Free Full Text]
  50. Wang GL, Jiang BH, Rue EA, Semenza GL: Hypoxia-inducible factor 1 is a basic-helix-loop-helix-PAS heterodimer regulated by cellular O2 tension. Proc Natl Acad Sci USA 1995, 92:5510-5514[Abstract/Free Full Text]
  51. Wang GL, Semenza GL: General involvement of hypoxia-inducible factor 1 in transcriptional response to hypoxia. Proc Natl Acad Sci USA 1993, 90:4304-4308[Abstract/Free Full Text]
  52. Reenstra WR, Yaar M, Gilchrest BA: Aging affects epidermal growth factor receptor phosphorylation and traffic kinetics. Exp Cell Res 1996, 227:252-255[Medline]
  53. Reenstra WR, Yaar M, Gilchrest BA: Effect of donor age on epidermal growth factor processing in man. Exp Cell Res 1993, 209:118-122[Medline]
  54. Liu Y, Guyton KZ, Gorospe M, Xu Q, Kokkonen GC, Mock YD, Roth GS, Holbrook NJ: Age-related decline in mitogen-activated protein kinase activity in epidermal growth factor-stimulated rat hepatocytes. J Biol Chem 1996, 271:3604-3607[Abstract/Free Full Text]
  55. Wheaton K, Atadja P, Riabowol K: Regulation of transcription factor activity during cellular aging. Biochem Cell Biol 1996, 74:523-534[Medline]
  56. Thakur MK, Oka T, Natori Y: Gene expression and aging. Mech Ageing Dev 1993, 66:283-298[Medline]
  57. Adams DH, Hathaway M, Shaw J, Burnett D, Elias E, Strain AJ: Transforming growth factor-beta induces human T lymphocyte migration in vitro. J Immunol 1991, 147:609-612[Abstract]
  58. Brandes ME, Mai UE, Ohura K, Wahl SM: Type I transforming growth factor-ß receptors on neutrophils mediate chemotaxis to transforming growth factor-ß. J Immunol 1991, 147:1600-1606[Abstract]
  59. Phillips GD, Whitehead RA, Knighton DR: Inhibition by methylprednisolone acetate suggests an indirect mechanism for TGF-B induced angiogenesis. Growth Factors 1992, 6:77-84[Medline]
  60. Noble NA, Harper JR, Border WA: In vivo interactions of TGF-beta and extracellular matrix. Prog Growth Factor Res 1992, 4:369-382[Medline]
  61. Kim SJ, Jeang KT, Glick AB, Sporn MB, Roberts AB: Promoter sequences of the human transforming growth factor-beta 1 gene responsive to transforming growth factor-beta 1 autoinduction. J Biol Chem 1989, 264:7041-7045[Abstract/Free Full Text]



This article has been cited by other articles:


Home page
 J Am Coll CardiolHome page
M. Bujak, H. J. Kweon, K. Chatila, N. Li, G. Taffet, and N. G. Frangogiannis
Aging-Related Defects Are Associated With Adverse Cardiac Remodeling in a Mouse Model of Reperfused Myocardial Infarction
J. Am. Coll. Cardiol., April 8, 2008; 51(14): 1384 - 1392.
[Abstract] [Full Text] [PDF]

Home page
 Cardiovasc ResHome page
M. Bujak and N. G. Frangogiannis
The role of TGF-{beta} signaling in myocardial infarction and cardiac remodeling
Cardiovasc Res, May 1, 2007; 74(2): 184 - 195.
[Abstract] [Full Text] [PDF]

Home page
 Toxicol PatholHome page
J. Yamate, Y. Machida, M. Ide, M. Kuwamura, T. Kotani, O. Sawamoto, and J. LaMarre
Cisplatin-Induced Renal Interstitial Fibrosis in Neonatal Rats, Developing as Solitary Nephron Unit Lesions
Toxicol Pathol, February 1, 2005; 33(2): 207 - 217.
[Abstract] [Full Text] [PDF]

Home page
 Arch SurgHome page
S. Coerper, C. Wicke, F. Pfeffer, G. Koveker, and H.-D. Becker
Documentation of 7051 Chronic Wounds Using a New Computerized System Within a Network of Wound Care Centers
Arch Surg, March 1, 2004; 139(3): 251 - 258.
[Abstract] [Full Text] [PDF]

Home page
 Arch SurgHome page
S. R. Bonomo, J. D. Davidson, J. W. Tyrone, X. Lin, and T. A. Mustoe
Enhancement of Wound Healing by Hyperbaric Oxygen and Transforming Growth Factor {beta}3 in a New Chronic Wound Model in Aged Rabbits
Arch Surg, October 1, 2000; 135(10): 1148 - 1153.
[Abstract] [Full Text] [PDF]

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wu, L.
Right arrow Articles by Mustoe, T. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wu, L.
Right arrow Articles by Mustoe, T. A.

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS