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From the Istituto Dermopatico dell’Immacolata,*Rome, Italy; the Department of Experimental Medicine,University of L’Aquila, L’Aquila, Italy; the Department of Medical Physiopathology,University La Sapienza, Rome, Italy; the Divisions of Haematology and Pathology,Ospedale Bambino Gesù, Rome, Italy; the Department of Pediatric Haematology and Oncology,¶Istituto di Ricovero e Cura a Carattere Scientifico Giannina Gaslini, Genova, Italy; the Institute of Biomedical Technology,**Consiglio Nazionale Delle Ricerche, Milan, Italy; the Department of Pediatrics,University Tor Vergata, Rome, Italy; and the Department of Medicine and Therapy,||University of Aberdeen, Aberdeen, Scotland
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Abstract |
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Vß3 receptor, c-Src, and PYK2 were unremarkable. Consistent with the finding in the bone biopsies, these cells excavated pits faintly stained with toluidine blue, indicating inefficient bone resorption. Bone marrow transplantation was successful in all patients, and posttransplant osteoclasts showed rescue of a3 subunit immunoreactivity.
The V-ATPase shares similarity with the F0-F1 ATP-synthase complex present in mitochondria, chloroplasts, and bacteria.5-8 It consists of a V0 transmembrane proton channel and a V1 ATP hydrolytic domain. The structure of the V1 complex is well defined. It is a 570-kd peripheral protein composed of eight subunits (A to H), with three copies of the A and B subunits and single copies of the remaining subunits. The V0 transmembrane domain contains five subunits (a, d, c, c', and c''), with six copies of c and c', and single copies of the others. c, c', and c'' subunits span the membrane and contribute to the organization of the proton channel. The a subunit is found in three isoforms, a1, a2, and a3, with the a3 being the one that is osteoclast-specific.5,9-11 Transcription of this subunit increases in resorption-competent osteoclasts and the protein is transferred to the ruffled border membrane during the process of cell polarization.12,13
The a subunit is a transmembrane glycoprotein possessing a large N-terminal hydrophilic domain and a C-terminal hydrophobic domain, containing multiple putative transmembrane helices. It has several buried charged residues that appear to be in a position to influence proton translocation. It also emerges to possess the binding site for the V-ATPase inhibitor bafilomycin.14,15
The osteoclast-specific a3 subunit of the V-ATPase is a 116-kd glycoprotein encoded by the ATP6i gene, also known as TCIRG1.16,17 Two transcripts arise from this gene. The OC116 is the osteoclast-specific form and is assembled from 20 exons. Another transcript, termed TIRC7, is more widely expressed. It starts from exon 5, has a translational start site located in exon 6, codon 217, and spans the remaining 14 exons.18 ATP6i-deficient mice, by homologous recombination, show severe osteopetrosis because of loss of osteoclast-mediated extracellular acidification.16,17 Likewise, the ATP6i gene has been found to posses recessive mutations in human osteopetrosis, and recent reports confirmed that this occurs in a large portion of the infantile malignant form of the disease.19-21
Human osteopetrosis is a severe heterogeneous genetic disorder, characterized by dense bones prone to fracture, severe hematological failure, and neural defects. However, all these forms have a common cellular defect, consisting in impaired osteoclast bone resorption.22,23
Various subtypes have been identified. The ATP6i-dependent one is the most common and is thought to account for 
50% of cases in autosomal-recessive osteopetrosis,19-21
followed by those dependent on mutations of the carbonic anhydrase type II (50 cases described to date)24
and of the ClC7 chloride channel (2 cases of malignant and 12 families of type II benign osteopetrosis).25,26
In many patients, however, the underlying genetic abnormality remains unclear.
Clinical manifestations of osteopetrosis are also highly variable, likely mirroring the genotype heterogeneity.22,23 Correlation of symptoms with the genetic background is still incomplete. For instance, the carbonic anhydrase type II mutation is responsible of a form also called "marble brain disease" because of cerebral calcifications. Patients also suffer from tubular acidosis because the carbonic anhydrase type II is strongly expressed by renal tubular cells.22-24 In the ClC7 mutation variant of the malignant osteopetrosis, retinal degeneration independent of optic nerve compression is likely to represent a specific stigma of the disease.25 Interestingly, this gene appears to also cause type II benign autosomal dominant osteopetrosis, a milder syndrome known as Albers-Schönberg disease, in which the mutant ClCN7 gene is thought to act as a dominant-negative gene, as opposed to the malignant form in which the loss-of-function mutation does not affect heterozygous individuals.26
Although ATP6i mutations account for most cases of autosomal recessive osteopetrosis, there is limited information on the correlation between genotype and phenotype, particularly at a cellular level. In view of this, the present study was designed to provide insights into the genetic, clinical, and cellular features in this form of the disease.
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Materials and Methods |
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Four patients affected by ATP6i-dependent autosomal recessive infantile osteopetrosis were analyzed in this study. A summary of clinical information is shown in Table 1
. The study abides by the rules of our Internal Review Board and the tenets of the Helsinki protocol.
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Cell culture media, serum, and reagents were from Gibco (Uxbridge, UK). Sterile glassware was from Falcon Becton Dickinson (Meylan, France). The anti-vß3 antibody, LM609, and the anti-Fc receptor (CD16) antibody were from Chemicon International Inc. (Temecula, CA). The anti pp60c-src polyclonal antibody and fluorescein isothiocyanate- or horseradish peroxidase-conjugated secondary antibodies were from Santa Cruz Biotechnology Inc. (Heidelberg, Germany). Antisera raised against the C-terminal peptide 811 to 829 (KFYSGTGYKLSPFTFAATD) of the a3 subunit of the osteoclast V-ATPase was kindly donated by Drs. J. P. Mattsson and D. Keeling (AstraZeneca, Mölndal, Sweden). The DNA extraction kit was from Stratagene (Amsterdam, The Netherlands). Reagents for polymerase chain reaction (PCR) were from Qiagen (Genenco, Florence, Italy). The nitrocellulose filter membrane and the chemiluminescence detection kit were from Amersham International plc (Chalfont Buckinghamshire, UK). Superscript II-reverse transcriptase was from Life Technologies (Milan, Italy). MwoI restriction enzyme was from New England Biolabs (Beverly, MA). Dye Terminator cycle sequencing ready reaction mix was from Perkin-Elmer Applied Biosystems (Foster City, CA). All other reagents were of the purest grade from Sigma Chemical Co. (St. Louis, MO).
Samples
Bone biopsies of the iliac crest were performed and processed for paraffin embedding. Sections were routinely stained with hematoxylin and eosin. Alternatively, sections were stained, as detailed below, to detect histochemically the tartrate-resistant acid phosphatase (TRAP) and immunocytochemically the a3 proton pump subunit.
When bone marrow samples were obtained for clinical purposes part of the material was used in this study. Bone marrow aspirates were also obtained from patient’s healthy relatives or unaffected age-matched controls. Peripheral blood samples were collected from patients and healthy donors. These materials were used with the informed consent of the patients or of their parents.
Mutation Analysis
DNA was extracted from ethylenediaminetetraacetic acid blood samples using a DNA extraction kit. The entire coding region of the 116-kd subunit was amplified using intronic primers deduced from sequence (GenBank accession number, AF033033), by the National Biosciences, Inc. OLIGO 4.1 Primer Analysis software. PCR reactions were performed using the Qiagen master mix kit, including 1x PCR buffer, 1x Q-solution, 200 µmol/L dNTP, 0.5 µmol/L primer pair, and 2.5 U/reaction Taq-DNA polymerase. Amplification conditions and primers are described in Table 2
. PCR products were purified using the Qiagen PCR purification kit (catalog no. 28104) following standard protocols recommended by the manufacturer. Ten ng of purified PCR were used for 100 bp of DNA cycle sequencing, which was performed using a Perkin-Elmer dye terminator cycle-sequencing ready reaction mix, using standard procedures. Reactions were applied to a Perkin-Elmer ABI 377 DNA sequencer. Sequences were aligned using the National Center for Biotechnology Information BLAST 2 program.
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RNA was extracted from ethylenediaminetetraacetic acid-peripheral blood samples using a standard phenol-chloroform method. For reverse transcriptase-PCR, 2 µg of total RNA were reverse-transcribed using Superscript II reverse transcriptase and one-tenth of the reaction product was used for PCR. This was performed in a final volume of 100 µl and 0.5 µmol/L of each primer (forward: 5'-GCT CGA TGG AGG AGG GAG TG-3'; reverse: 5'-GTA AGC ATC GTG TGC TGG GC-3'). Samples were then subjected to 2.5% agarose gel electrophoresis using 1x TAE running buffer (0.04 mol/L Tris-acetate, 0.001 mol/L ethylenediaminetetraacetic acid) to verify PCR quality. For restriction fragment length polymorphism analysis, PCR products were then purified by the Qiagen PCR purification kit and digested with 1 U/µg of restriction enzyme MwoI (restriction enzyme analysis, http://darwin.bio.geneseo.edu/yin/WebGene/RE.html), at 60°C for 3 hours. Digestion was assessed by ethidium bromide-2.5% agarose gel electrophoresis and ultraviolet transillumination.
Western Blot
Cells were washed twice with phosphate-buffered saline (PBS) and lysed in a buffer containing 50 mmol/L Hepes (pH 7.2), 150 mmol/L NaCl, 10% glycerol, 1% Triton X-100, 1.5 mmol/L MgCl2, 5 mmol/L EGTA, 50 mmol/L NaF, 100 µmol/L sodium vanadate, 10 µg/ml aprotinin, 10 µg/ml leupeptin, 1 mmol/L phenylmethylsulfonyl fluoride. Lysates were centrifuged at 14,000 rpm at 4°C for 10 minutes, and protein were measured by the Bradford method. Eighty µg of protein in reducing sample buffer was subjected to 10% sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Proteins were then transferred to nitrocellulose filter papers and incubated with primary antibody diluted 1:1000 in TBST buffer (25 mmol/L Tris-buffered saline, pH 7.4, 0.05% Tween), containing 1% nonfat milk, at room temperature for 1 hour. Filters were washed three times in TBST buffer and then incubated with secondary antibody diluted 1:10,000 in TBST buffer containing 1% nonfat milk, at room temperature for 1 hour. Bands were revealed by the enhanced chemiluminescence detection kit.
Osteoclast Preparation from Bone Marrow
The total bone marrow cell fraction was dispersed in Iscove’s modified minimum essential medium supplemented with 20% fetal calf serum, 100 U/ml penicillin, and 100 µg/ml streptomycin, and cultured in plastic dishes at 37°C in a humidified atmosphere of 95% air and 5% CO2. After 24 hours, nonadherent cells were removed by aspiration and extensive washing.
Osteoclast Preparation from Peripheral Blood Monocytes
Peripheral blood mononuclear cells were prepared from human blood diluted in Hanks’ balanced salt solution (1:1). Diluted blood was layered over Histopaque 1077 solution, centrifuged at 400 x g for 30 minutes, then washed twice with Hanks’ solution and centrifuged at the speed as above for 10 minutes. Cells were resuspended in Dulbecco’s modified Eagle’s medium containing 4 mmol/L of L-glutamine, 100 U/ml of penicillin, 100 µg/ml of streptomycin, and 10% fetal calf serum. Cells (3 x 106 cells/cm2) were plated on glass coverslips or bone slices and incubated at 37°C in a humidified atmosphere with 5% CO2. After 1 hour, cell cultures were rinsed to remove nonadherent cells and were maintained in medium as above in the presence of 25 ng/ml of recombinant human macrophage colony stimulating factor, 30 ng/ml of recombinant human receptor activator of NF-
B ligand, and 100 nmol/L of parathyroid hormone (PTH) for 21 days. Medium and factors were replaced every 3 to 4 days.
TRAP Activity
Cells were fixed in 3% paraformaldehyde in 0.1 mol/L of cacodylate buffer for 15 minutes, then extensively washed in the same buffer. TRAP activity was detected histochemically in cells or in paraffin-embedded sections of the bone biopsies, using the Sigma-Aldrich kit no. 386, according to the manufacturer’s instruction.
Bone Resorption Assay
Cells were cultured in 24-plate multiwells containing 4 x 4-mm bovine bone slices, and fixed in 3% paraformaldehyde in PBS, then slices were cleaned free of cells by sonication, stained with 1% toluidine blue, and observed by conventional light microscopy.
Immunocytochemistry and Fluorescence Microscopy
Cells plated on glass coverslips were fixed with 4% paraformaldehyde in PBS at 4°C for 10 minutes, washed three times in PBS, then, when required, permeabilized with 0.05% Triton X-100 in PBS at 4°C for 10 minutes and incubated in 1% bovine serum albumin at room temperature for 15 minutes. Samples were incubated at 37°C for 1 hour with a3, c-Src, vß3 integrin, and PYK2 antibodies, then washed with PBS, followed by TRITC- or horseradish peroxidase-conjugated anti-mouse or anti-rabbit secondary antibody at 37°C for 1 hour. Microfilaments were decorated by incubation with 5 µg/ml of TRITC-conjugated phalloidin at 37°C for 1 hour. Samples were viewed with conventional light or epifluorescence in a Zeiss Axioplan microscope (Jena, Germany).
Quantitative Analysis
Bone resorption was determined by pit enumeration. Histochemical TRAP staining intensity was determined by densitometry and indicated as arbitrary units. Quantitative data were expressed as mean ± SEM. Statistics was computed by the Student’s t-test and a P < 0.05 was conventionally considered significant.
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Results |
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TopAbstractMaterials and MethodsResultsDiscussionReferences |
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Mutation analysis was performed sequencing all of the 20 coding exons and intron junctions after amplification from genomic DNA, and ATP6i mutations were identified in these patients (Figure 1)
. A summary of mutations is shown in Table 3
. Patient 1 was homozygous for a mutation in exon 11 consisting of a single G nucleotide deletion that predicted a frameshift and truncation of the protein in the I/II transmembrane domain. Patient 2 was homozygous for a C/A transversion in exon 13 that is predicted to introduce a stop codon in the III/IV transmembrane domains. Patient 3 was a compound heterozygote, carrying single point mutations affecting the acceptor splice site of intron 14 and the last nucleotide of exon 18. The mutation in intron 14 (G/A transition) was predicted to determine putative abnormal splicing in loop IV/V, whereas mutation in exon 18 (C/T transition) could give rise either to abnormal splicing or to protein truncation in the VIII transmembrane domain. In patient 4, there was a homozygous splice donor site mutation in intron 18 that is predicted to determine abnormal splicing in the VIII transmembrane domain (Figure 1
, Table 3
). To the best of our knowledge, the mutations found in patients 1 and 2, and that in exon 18 of patient 3 are novel and had not been previously described.
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, MwoI restriction enzyme, cutting gcnnnnn/nngc sequences, was predicted to digest amplified wild-type cDNA in nine fragments of 14 to 146 bp, spanning nucleotides 1073 to 1558 of exons 10 to 12. In patient 1, the G deletion predicted in cDNA position 1285 would determine the appearance of an additional MwoI restriction cut site (Figure 2)
. Therefore, 10 fragments of 14 to 109 bp were expected to be formed in this patient. This resulted to be the case, as in Figure 2
two fragments of 87 bp and 58 bp were observed in the patient, but not in the control. In contrast, the 146-bp fragment apparent in the control subject was not observed in the patient.
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shows that peripheral blood mononuclear cells harvested from a control subject express high amounts of the TIRC7 protein, derived by alternative splicing of the ATP6i gene, which is known to play a relevant role in lymphocyte activation.18
Long film exposure demonstrated also faint expression in these cells of the 116-kd a3 subunit. In contrast, proteins extracted from peripheral blood mononuclear cells of patient 1 failed to immunoreact with this antibody, confirming lacking of the protein C-terminal sequence.
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Clinical follow-up was available for our patients (Table 1)
. Symptoms were quite variable, however all patients shared macrocephaly, growth retardation, and compromised vision because of optic nerve compression syndrome. Three patients also showed hepatosplenomegaly. Laboratory findings (Table 4)
revealed severe anemia and altered white cell counts in all patients, whereas platelet counts were low only in one patient. Interestingly, all patients shared mild to severe hypocalcemia, and elevated serum alkaline phosphatase activity and PTH levels. When available, total creatinine kinase enzyme was unremarkable. Radiographs showed a generalized increase in bone density, sclerosis of the basis of the skull with increased density of the orbits (Figure 4A)
. Proximal metaphyses of femurs and tibias were irregularly shaped (Figure 4B)
and, together with forearms, showed diffused osteosclerosis and absence of medullary cavities (Figure 4, B and C)
. Femurs, tibias, forearms, phalanges, (Figure 4; B to D)
and iliac crests (not shown) showed endobone appearance.
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. Nine months post-BMT (which was received at the age of 6 months), patient 1 shows a mild osteosclerotic pattern. Patient 2 was transplanted 1 year ago at the age of 22 months. She still shows growth retardation and post-BMT hypercalcemia.22
Patient 3 was transplanted 2.5 years ago at the age of 9 months. This patient had severe optic nerve failure, which was not rescued by BMT. Because of positive family history, patient 4 was investigated at birth and received an early diagnosis. Pre-BMT evoked visual potential analysis had revealed bilateral severely compromised optic nerve function. This patient was transplanted 5 years ago at the age of 2 months and underwent surgery for optic channel decompression. Now he is healthy, with normal growth rate. The right eye completely rescued its function, whereas the left eye still presents remarkable reduced vision (<1/50). Bone Biopsies
A clear-cut osteosclerotic pattern was obvious in sections of iliac crest biopsies of all patients (Figure 5)
. Bone trabeculae were massive and irregular in shape. In some of them inner cores of unresorbed mineralized cartilage (endochondral trabeculae) (Figure 5, B and H)
were noticed. Several osteoclasts noted for their large size, multinuclearity (average, four to seven nuclei per cell; Figure 5
), and positivity to TRAP activity (Figure 6)
were associated with the trabecular profiles. These osteoclasts showed apparent normal polarization and contact with bone (Figure 5)
. Some of them laid in shallow Howship lacunae, indicating that some resorption of bone could take place (Figure 5H)
. Some trabeculae were layered by active matrix-forming osteoblasts (not shown). Hematopoietic tissue was scarce against a remarkable background of diffuse fibrosis (Figure 5)
.
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Growth of bone marrow cells from patient 1 resulted in the immediate appearance of a population of giant cells, phenotypically indistinguishable from multinucleated osteoclasts. These cells attached to the culture dish in a few hours and showed a highly motile phenotype underlined by the appearance of well-developed lamellipodia in their paramarginal area (Figure 8A)
. Similar to what was observed in the iliac crest biopsy, giant cells had an average number of nuclei ranging from four to seven, with prominent nucleoli. Nuclei were located in the cell center together with organelles and vacuoles of variable size. As expected, no giant cells were readily apparent in the cultures of the healthy sister of this patient and of control donors (not shown). Long-term cultures resulted in the overgrowth of a stromal-like cell population, both in the patient and in the normal controls. However, histochemical staining revealed the presence of TRAP-positive giant cells only in the patient (Figure 8B)
, whereas, as already described,27
in the cultures of controls no TRAP-positive cells or only TRAP-positive putative mononuclear osteoclast precursors were observed (not shown). Despite the large numbers of osteoclasts in the bone marrow culture of the patient, only small pits could be detected (Figure 8C)
, thus indicating a failure in the resorbing function of the giant cells.
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. In both cultures, giant cells appeared disk-shaped, with a clear zone-like paramarginal area, nuclei and organelles were unremarkable. A strong TRAP activity was apparent in the giant cells from the patient (Figure 9, B and C)
. Enzyme distribution in perinuclear vesicles was identical to control cells, however stain intensity was twofold higher in diseased relative to normal osteoclasts (Figure 9; A to C)
(quantitative analysis, arbitrary units ± SEM: control, 10.8 ± 0.57; patient, 20.1 ± 1.13; n = 5; P < 0.001). Interestingly, osteoclasts harvested from patient 1 after BMT that were supposed to derive from the donor showed TRAP staining apparently lower than in pre-BMT osteoclasts (Figure 9, C and D)
. Notably, although control osteoclasts immunostained with the antisera raised against the C-terminal peptide of the a3 subunit of the osteoclast V-ATPase the osteoclasts from the patient were immunonegative. Osteoclasts harvested from patient 1 after BMT showed rescue of the immunoreactivity (not shown).
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, those excavated by osteopetrotic osteoclasts appeared very pale indicating that little organic matrix was exposed (Figure 9F)
. However, the number of pits was similar in the control and in the patient (number/section: control, 24.6 ± 1.94; patient, 22.8 ± 0.88; n = 3; n.s.). Together with the observation in the bone biopsies, these findings indicate that in ATP6i-dependent osteopetrosis, osteoclast bone resorption is severely compromised but not completely absent.
Consistent with the normal polarization of osteoclasts observed in the iliac crest biopsies, osteoclasts harvested from the peripheral blood monocytes of the patients did not show remarkable alteration of cytoskeletal arrangement and podosome distribution. Fluorescent phalloidin staining revealed normal actin rings with typical punctate patterns as also observed in control cells (Figure 10, A and B)
. Membrane distribution of the vitronectin Vß3 integrin receptor was unremarkable (Figure 10, C and D)
. Thus, at variance with previous observations by us and others,27,28
and similar to what observed by Flanagan and colleagues29
in patients affected by malignant osteopetrosis of unknown genetic origin, no obvious alteration of the adhesion and polarization patterns is observed in our ATP6i-dependent patients. Consistently, in the osteopetrotic osteoclasts PYK2 and c-Src appeared normally distributed at the paramarginal area overlapping the actin ring (Figure 10, E and F)
where these tyrosine kinases are supposed to contribute to integrin-mediated osteoclast adhesion and outside-in signaling.
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Discussion |
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TopAbstractMaterials and MethodsResultsDiscussionReferences |
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Previous reports have indicated that ATP6i mutations account for most cases of autosomal-recessive osteopetrosis19-21 and in our studies, this gene was mutated in all four patients. In three cases, the ATP6i gene mutations discovered were novel (exon 9, DelG8521; exon 13, C8980A; exon 18, C11278T). Interestingly, in all cases investigated so far, 20% of the alleles were found to carry a G10106A transition in intron 14 leading to abnormal splicing, suggesting that this could be a candidate hot spot for mutations.21
In this study all patients showed high alkaline phosphatase and PTH serum levels. These two biochemical findings are inconsistently present in osteopetrosis and reports can be contradictory.22,30,31 The elevated alkaline phosphatase activity could depend on altered osteoblast function.32 This biochemical marker is higher in children than in adults, reflecting elevated bone formation for skeletal growth.33 Its further increase in infants with osteopetrosis does not have a definitive explanation yet. Osteopetrosis is regarded as an osteoclast disease. However, some extent of osteosclerosis, namely increased osteoblast activity and bone formation, has been claimed to occur in this disease,34,35 and in our iliac crest biopsies, active osteoblasts are seen in patients. This event is not easily explainable if the osteoclast-osteoblast coupling is taken in account. However, it must be considered that during skeletal development, osteoclast and osteoblast activities are often uncoupled, as it occurs, for instance, during periosteal bone formation associated to endosteal bone resorption to increase diaphyseal collar size accompanied by enlargement of medullary cavity.36
Most forms of the disease in humans display increased numbers of osteoclasts. In our patients, this was a constant and obvious feature in bone biopsies, and others have reported similar findings.37,38 In the past, insensitivity of osteoclasts and osteoblasts to the effects of PTH was thought to be a cause of osteopetrosis.39-42 In the light of recent data,43 we speculate that the increased PTH levels are a result of the disease, because of the hypocalcemia that presumably depends on ineffective bone resorption. The increased osteoclast formation and bone formation that was observed could simply be a reflection of the elevated PTH levels, which also could contribute, in three of our patients, to maintain serum calcium values close to the normal ranges by its action on other organs (ie, the kidney).
Osteoclast morphology in our patients seems to be normal. Lack of ruffled border is claimed to be a common feature of osteopetrotic osteoclasts. Unfortunately, we could not address this issue in our study because of the lack of electron microscope samples of bone biopsies. Nevertheless, relative to another case of osteopetrosis investigated in our laboratory,27 where the ruffled borders of the osteoclasts were lacking and the adhesion properties altered, the osteoclasts of our ATP6i-positive patients showed no obvious morphological alterations by routine histology. Holliday and colleagues12 and Lee and colleagues13 have demonstrated that the mouse osteoclast V-ATPase interacts with microfilaments during bone resorption and proposed that proton transport by this pump is associated with reorganization of the actin cytoskeleton during osteoclast activation. However, this interaction seems to depend on the B subunits of the V-ATPase, therefore it is not surprising that no cytoskeletal rearrangements or abnormal polarization is observed in the osteoclasts of our patients.
Interestingly, bone biopsies showed intensely TRAP-positive osteoclasts placed in altered resorption lacunae, which we believe to represent the result of impaired, but still remarkable, bone resorption. This result was confirmed in our in vitro assay, in which toluidine blue staining demonstrated similar pit numbers, although little organic matrix was exposed in the pits excavated by the osteoclasts of our patient. We believe that it would be remarkable to investigate the molecular mechanisms that could complement a3 activity, ie, other a subunits, or other proton extrusion devices, such as the Na+/H+ anti-port. It is interesting to note that redundant activities are often observed in bone cells, and double-knockout experiments are sometime required to disclose effective functions of given genes.44 We believe that such a knowledge in a3-deficient osteoclasts could be helpful for future pharmacological management of the disease.
Interestingly, TRAP-activity was found to be elevated in patients’ osteoclasts. Unfortunately, this marker has not been evaluated in the sera of these patients, therefore we cannot address the issue of whether a correlation exists between the cellular and the clinical findings. Notably, TRAP-activity was less pronounced in post-BMT osteoclasts harvested from the monocytic fraction of peripheral blood of patients. We believe that these are donor osteoclasts because of the fact that these osteoclasts are now positive to the a3 subunit of the V-ATPase. Clinical follow-up of this patient shows so far a marked amelioration of skeletal, hematological, and biochemical symptoms, thus confirming our hypothesis.
One of the means whereby we tested integrity of the ATP6i gene in one patient was the analysis of the TIRC7 protein in lymphocytes.18,45,46
This is a novel ATP6i gene product consisting of an 75-kd transmembrane protein expressed in the early stages of T-cell activation, which does not share structural or sequence homology with any of the known T-cell accessory molecules.18
TIRC7 expression increases during acute rejection of cardiac allografts,45,46
however its molecular and cellular roles are at present still unclear. Despite this, detection of TIRC7 expression could be used as a valid tool for a rapid diagnosis of ATP6i-dependent osteopetrosis, at least in those cases in which the genetic mutation leads to loss of the a3/TIRC7 C-terminus (the majority so far). In addition, antibodies against TIRC7 inhibit in vitro proliferation and Th1-type cytokine production by activated human T cells,47
thus representing an additional tool to investigate alteration of this gene in osteopetrotic patients. Further insights into the TIRC7 protein structure and function are however necessary to fully understand its role in lymphocytes and in other cell types.
In conclusion, we described genetic, clinical, and cellular findings in four individuals affected by ATP6i-dependent autosomal-recessive infantile osteopetrosis. We believe that this genotype/phenotype correlation will help future developments of successful management, including cell and gene therapy.
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Acknowledgements |
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Footnotes |
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Supported by the Telethon (grant E.0831), the Fondo per gli Investimenti per la Ricerca di Base (grant RBAU01X3NH), the University of L’Aquila (to A. T.), and by the Ministero della Salute (grant code 0002P70), Ricerca Corrente to Ospedale Bambino Gesù.
Accepted for publication September 11, 2002.
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K. Henriksen, J. Gram, S. Schaller, B. H. Dahl, M. H. Dziegiel, J. Bollerslev, and M. A. Karsdal Characterization of Osteoclasts from Patients Harboring a G215R Mutation in ClC-7 Causing Autosomal Dominant Osteopetrosis Type II Am. J. Pathol., May 1, 2004; 164(5): 1537 - 1545. [Abstract] [Full Text] [PDF]
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 U. H. Lerner NEW MOLECULES IN THE TUMOR NECROSIS FACTOR LIGAND AND RECEPTOR SUPERFAMILIES WITH IMPORTANCE FOR PHYSIOLOGICAL AND PATHOLOGICAL BONE RESORPTION Critical Reviews in Oral Biology & Medicine, March 1, 2004; 15(2): 64 - 81. [Abstract] [Full Text] [PDF]
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