help button home button Am J Pathol Epitomics
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text
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 Tobin, D. J.
Right arrow Articles by Paus, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tobin, D. J.
Right arrow Articles by Paus, R.
(American Journal of Pathology. 2002;160:1807-1821.)
© 2002 American Society for Investigative Pathology


Regular Articles

The Lysosomal Protease Cathepsin L Is an Important Regulator of Keratinocyte and Melanocyte Differentiation During Hair Follicle Morphogenesis and Cycling

Desmond J. Tobin*, Kerstin Foitzik{dagger}, Thomas Reinheckel{ddagger}, Lars Mecklenburg{dagger}, Vladimir A. Botchkarev§, Christoph Peters{ddagger} and Ralf Paus{dagger}

From the Department of Biomedical Sciences,*University of Bradford, Bradford, England; the Department of Dermatology,{dagger}University Hospital Hamburg-Eppendorf, University of Hamburg, Hamburg, Germany; the Institute of Molecular Medicine,{ddagger}University of Freiburg, Freiburg, Germany; and the Department of Dermatology,§Boston University School of Medicine, Boston, Massachusetts

We have previously shown that the ubiquitously expressed lysosomal cysteine protease, cathepsin L (CTSL), is essential for skin and hair follicle homeostasis. Here we examine the effect of CTSL deficiency on hair follicle development and cycling in ctsl-/- mice by light and electron microscopy, Ki67/terminal dUTP nick-end labeling, and trichohyalin immunofluorescence. Hair follicle morphogenesis in ctsl-/- mice was associated with several abnormalities. Defective terminal differentiation of keratinocytes occurred during the formation of the hair canal, resulting in disruption of hair shaft outgrowth. Both proliferation and apoptosis levels in keratinocytes and melanocytes were higher in ctsl-/- than in ctsl+/+ hair follicles. The development of the hair follicle pigmentary unit was disrupted by vacuolation of differentiating melanocytes. Hair cycling was also abnormal in ctsl-/- mice. Final stages of hair follicle morphogenesis and the induction of hair follicle cycling were retarded. Thereafter, these follicles exhibited a truncated resting phase (telogen) and a premature entry into the first growth phase. Further abnormalities of telogen development included the defective anchoring of club hairs in the skin, which resulted in their abnormal shedding. Melanocyte vacuolation was again apparent during the hair cycle-associated reconstruction of the hair pigmentary unit. A hallmark of these ctsl-/- mice was the severe disruption in the exiting of hair shafts to the skin surface. This was mostly because of a failure of the inner root sheath (keratinocyte layer next to the hair shaft) to fully desquamate. These changes resulted in a massive dilation of the hair canal and the abnormal routing of sebaceous gland products to the skin surface. In summary, this study suggests novel roles for cathepsin proteases in skin, hair, and pigment biology. Principal target tissues that may contain protein substrate(s) for this cysteine protease include the developing hair cone, inner root sheath, anchoring apparatus of the telogen club, and organelles of lysosomal origin (eg, melanosomes).





This article has been cited by other articles:


Home page
Am. J. Physiol. Cell Physiol.Home page
X. Zheng, F. Chu, P. M. Chou, C. Gallati, U. Dier, B. L. Mirkin, S. A. Mousa, and A. Rebbaa
Cathepsin L inhibition suppresses drug resistance in vitro and in vivo: a putative mechanism
Am J Physiol Cell Physiol, January 1, 2009; 296(1): C65 - C74.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
D. Spira, J. Stypmann, D. J. Tobin, I. Petermann, C. Mayer, S. Hagemann, O. Vasiljeva, T. Gunther, R. Schule, C. Peters, et al.
Cell Type-specific Functions of the Lysosomal Protease Cathepsin L in the Heart
J. Biol. Chem., December 21, 2007; 282(51): 37045 - 37052.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Pathol.Home page
E. Bodo, D. J. Tobin, Y. Kamenisch, T. Biro, M. Berneburg, W. Funk, and R. Paus
Dissecting the Impact of Chemotherapy on the Human Hair Follicle: A Pragmatic in Vitro Assay for Studying the Pathogenesis and Potential Management of Hair Follicle Dystrophy
Am. J. Pathol., October 1, 2007; 171(4): 1153 - 1167.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
T. Cheng, K. Hitomi, I. M. J. J. van Vlijmen-Willems, G. J. de Jongh, K. Yamamoto, K. Nishi, C. Watts, T. Reinheckel, J. Schalkwijk, and P. L. J. M. Zeeuwen
Cystatin M/E Is a High Affinity Inhibitor of Cathepsin V and Cathepsin L by a Reactive Site That Is Distinct from the Legumain-binding Site: A NOVEL CLUE FOR THE ROLE OF CYSTATIN M/E IN EPIDERMAL CORNIFICATION
J. Biol. Chem., June 9, 2006; 281(23): 15893 - 15899.
[Abstract] [Full Text] [PDF]


Home page
FASEB J.Home page
I. Petermann, C. Mayer, J. Stypmann, M. L. Biniossek, D. J. Tobin, M. A. Engelen, T. Dandekar, T. Grune, L. Schild, C. Peters, et al.
Lysosomal, cytoskeletal, and metabolic alterations in cardiomyopathy of cathepsin L knockout mice
FASEB J, June 1, 2006; 20(8): 1266 - 1268.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
E. Legue and J.-F. Nicolas
Hair follicle renewal: organization of stem cells in the matrix and the role of stereotyped lineages and behaviors
Development, September 15, 2005; 132(18): 4143 - 4154.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
T. Reinheckel, S. Hagemann, S. Dollwet-Mack, E. Martinez, T. Lohmuller, G. Zlatkovic, D. J. Tobin, N. Maas-Szabowski, and C. Peters
The lysosomal cysteine protease cathepsin L regulates keratinocyte proliferation by control of growth factor recycling
J. Cell Sci., August 1, 2005; 118(15): 3387 - 3395.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
G. Lombardi, D. Burzyn, J. Mundinano, P. Berguer, P. Bekinschtein, H. Costa, L. F. Castillo, A. Goldman, R. Meiss, I. Piazzon, et al.
Cathepsin-L Influences the Expression of Extracellular Matrix in Lymphoid Organs and Plays a Role in the Regulation of Thymic Output and of Peripheral T Cell Number
J. Immunol., June 1, 2005; 174(11): 7022 - 7032.
[Abstract] [Full Text] [PDF]


Home page
J. Histochem. Cytochem.Home page
S. Nishikawa
Presence of Anti-cystatin C-positive Dendritic Cells or Macrophages and Localization of Cysteine Proteases in the Apical Bud of the Enamel Organ in the Rat Incisor
J. Histochem. Cytochem., May 1, 2005; 53(5): 643 - 651.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Pathol.Home page
U. Guha, L. Mecklenburg, P. Cowin, L. Kan, W. M. O'Guin, D. D'Vizio, R. G. Pestell, R. Paus, and J. A. Kessler
Bone Morphogenetic Protein Signaling Regulates Postnatal Hair Follicle Differentiation and Cycling
Am. J. Pathol., September 1, 2004; 165(3): 729 - 740.
[Abstract] [Full Text] [PDF]


Home page
Mol. Pharmacol.Home page
J. A. Caruso, P. A. Mathieu, A. Joiakim, B. Leeson, D. Kessel, B. F. Sloane, and J. J. Reiners Jr.
Differential Susceptibilities of Murine Hepatoma 1c1c7 and Tao Cells to the Lysosomal Photosensitizer NPe6: Influence of Aryl Hydrocarbon Receptor on Lysosomal Fragility and Protease Contents
Mol. Pharmacol., April 1, 2004; 65(4): 1016 - 1028.
[Abstract] [Full Text]


Home page
J. Biol. Chem.Home page
P. M. Steinert, D. A. D. Parry, and L. N. Marekov
Trichohyalin Mechanically Strengthens the Hair Follicle: MULTIPLE CROSS-BRIDGING ROLES IN THE INNER ROOT SHEATH
J. Biol. Chem., October 17, 2003; 278(42): 41409 - 41419.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
S. Yasothornsrikul, D. Greenbaum, K. F. Medzihradszky, T. Toneff, R. Bundey, R. Miller, B. Schilling, I. Petermann, J. Dehnert, A. Logvinova, et al.
Cathepsin L in secretory vesicles functions as a prohormone-processing enzyme for production of the enkephalin peptide neurotransmitter
PNAS, August 5, 2003; 100(16): 9590 - 9595.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2002 by the American Society for Investigative Pathology.