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Research Article

Mice lacking β3 integrins are osteosclerotic because of dysfunctional osteoclasts

Kevin P. McHugh1, Kairbaan Hodivala-Dilke2, Ming-Hao Zheng1,3, Noriyuki Namba1, Jonathan Lam1, Deborah Novack1, Xu Feng1, F. Patrick Ross1, Richard O. Hynes2 and Steven L. Teitelbaum1

1Department of Pathology, Washington University School of Medicine, St. Louis, Missouri 63110, USA
2Howard Hughes Medical Institute, Center for Cancer Research and Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA
3Department of Orthopedic Surgery, University of Western Australia, Nedlands, Western Australia 6009, Australia

Address correspondence to: Steven L. Teitelbaum, Washington University School of Medicine, Barnes-Jewish Hospital North, 216 South Kingshighway, Mail Stop 9031649, St. Louis, Missouri 63110, USA. Phone: (314) 454-8463; Fax: (314) 454-5505; E-mail: teitelbs@medicine.wustl.edu.

Published February 15, 2000
Received for publication November 11, 1999, and accepted in revised form January 10, 2000.

Osteoclasts express the αvβ3 integrin, an adhesion receptor that has been implicated in bone resorption and that is therefore a potential therapeutic target. To assess the role of this heterodimer in skeletal development in vivo, we engineered mice in which the gene for the β3 integrin subunit was deleted. Bone marrow macrophages derived from these mutants differentiate in vitro into numerous osteoclasts, thus establishing that αvβ3 is not necessary for osteoclast recruitment. Furthermore, the closely related integrin, αvβ5, does not substitute for αvβ3 during cytokine stimulation or authentic osteoclastogenesis. β3 knockout mice, but not their heterozygous littermates, develop histologically and radiographically evident osteosclerosis with age. Despite their increased bone mass, β3-null mice contain 3.5-fold more osteoclasts than do heterozygotes. These mutant osteoclasts are, however, dysfunctional, as evidenced by their reduced ability to resorb whale dentin in vitro and the significant hypocalcemia seen in the knockout mice. The resorptive defect in β3-deficient osteoclasts may reflect absence of matrix-derived intracellular signals, since their cytoskeleton is distinctly abnormal and they fail to spread in vitro, to form actin rings ex vivo, or to form normal ruffled membranes in vivo. Thus, although it is not required for osteoclastogenesis, the integrin αvβ3 is essential for normal osteoclast function.

Introduction

The osteoclast, a polykaryon of monocyte/macrophage origin, is probably the exclusive resorptive cell of bone. As any type of osteoporosis always reflects enhanced resorption relative to formation, the osteoclast has been a principal therapeutic target in circumstances of diminished bone mass. In fact, all successful antiosteoporosis agents identified to date target the osteoclast.

Despite success achieved with antiresorptive drugs such as estrogen and newer compounds like bisphosonates, each carries, unfortunately, the potential for substantial complications. However, recent years have witnessed identification of novel, osteoclast-expressed molecules that may serve as potential therapeutic targets. The success of this search is reflective of the insights gained into osteoclast formation mechanisms and the means by which the cell resorbs bone. It is now known that osteoclasts differentiate from monocyte/macrophage precursors under the influence of 2 essential molecules, namely the receptor activator of NF-κB ligand (RANKL) (equivalent to osteoprotegerin ligand) and the macrophage colony stimulating factor (M-CSF) (1). When the differentiated polykaryon contacts bone, it undergoes cytoskeletal reorganization eventuating in polarization of its resorptive apparatus to the cell-bone interface creating, thereof, an isolated, resorptive microenvironment (2). Thus, matrix-derived intracellular signals and physical intimacy of the osteoclast with underlying bone, are central to the cell’s capacity to degrade the skeleton. Hence, osteoclast-residing, matrix attachment molecules — particularly those capable of transmitting matrix-derived signals — might serve as potential antiosteoporosis targets.

Based on blocking experiments, the αvβ3 integrin has been identified as a major functional adhesion receptor on osteoclasts. Specifically, inhibitors of αvβ3, particularly peptides or peptidomimetics, reduce the capacity of osteoclasts to bind to and resorb bone (3, 4). These observations suggest that αvβ3 plays a major role in osteoclast function (3, 4) and generation (5), and that inhibitors of this integrin may be useful in preventing osteoporosis (4).

By application of similar inhibitors, αvβ3 has also been implicated in angiogenesis (6). Genetic ablation of either αv (7) or β3 (8) fails, however, to block angiogenesis. Thus, despite observations made with αvβ3 inhibitors, these studies not only establish that αvβ3 is not essential for angiogenesis, but also raise questions regarding the validity of the osteoclast-based blocking experiments. This conundrum, taken with the possibility that αvβ3 may indirectly regulate the functions of other integrins by so-called “transdominant regulation” (9), indicates that further exploration of the role of αvβ3 in osteoclastic bone resorption is essential. To that end, we generated β3–/– mice using a targeting construct in which a 1.2-kb genomic fragment (including 300 bp of the promoter, the transcriptional start site, exon I, intron I, and exon II) is replaced by a phosphoglycerokinase promoter-neomycin resistance gene cassette (8). β3-null mice are viable and exhibit the bleeding disorders expected as a consequence of their lack of αIIbβ3 integrin on platelets (8). Here we report our analyses of bone structure and metabolism in these mice. Our findings demonstrate that although αvβ3 crucially — but incompletely — regulates osteoclast function (which is in contrast to results obtained with inhibitors of the integrin [5]), it is not necessary for osteoclast generation.

Methods

Materials. Recombinant murine IL-4 and GM-CSF were purchased from Genzyme Pharmaceuticals (Cambridge, Massachusetts, USA). 1,25-Dihyroxyvitamin D3 was a gift of Milan Uscosovich (Hoffman LaRoche Inc., Nutley, New Jersey, USA). Murine M-CSF was generated and purified in our laboratory as described previously (10). Glutathione-S-transferase (GST)-RANKL was expressed in our laboratory. The GST-RANKL vector was constructed by PCR cloning a SalI/NotI fragment corresponding to amino acids 158–316 of murine RANKL from osteoblast cDNA (forward primer: 5′-ATGTGGCCCGTCGACGCAAGCCTGAGGCCCAGCC-3′; reverse primer: 5′-AAACATCTAGGGCGGCCGCGCTAATG-3′) and cloning into pGEX-4T-1 (Amersham Pharmacia Biotech, Piscataway, New Jersey, USA). Both strands were sequenced. High-expressing BL21 (Stratagene, La Jolla, California, USA) cells were lysed under nondenaturing conditions and GST-RANKL was purified over a glutathione-Sepharose column followed by ion exchange chromatography.

Osteoclast generation. Bone marrow macrophages (BMMs) were isolated from whole marrow of 4- to 8-week-old mice, cultured overnight, and then subjected to Ficoll-Hypaque gradient purification as described (11). Cells at the gradient interface were collected and cultured on tissue culture plates or dentin slices at a 10:1 ratio with the ST2 stromal cell line in α minimal essential medium containing 1,25-dihydroxyvitamin D3 and glucocorticoids, supplemented with 10% heat-inactivated fetal bovine serum at 37°C with 5% CO2 (12). In some experiments, pure populations of BMMs (13) were maintained with RANKL (100 ng/mL) and M-CSF (10 ng/mL), which induces these cells to undergo osteoclast differentiation (1).

Histology. Mouse femurs were excised, cleaned of soft tissue, and decalcified in EDTA. Histologic sections were stained with hematoxylin and eosin or for tartrate-resistant acid phosphatase (TRAP) activity using a commercial kit (Sigma Chemical Co., St. Louis, Missouri, USA). Generated osteoclasts were stained for TRAP activity using the same kit. The number of osteoclasts per millimeter surface of trabecular bone was determined using the Bioquant system (R&M Biometrics, Nashville, Tennessee, USA).

Cell surface protein biotinylation. For 5 days, 107 BMMs were grown in α-MEM + 10% FCS containing 1,000 U/mL M-CSF (stage-1) and then treated with IL-4 (5 ng/mL) (R & D Systems Inc., Minneapolis, Minnesota, USA) or vehicle for an additional 48 hours. Cells were washed in PBS-0.1M HEPES, and cell surface proteins were biotinylated using n-hydroxysuccinimide-biotin (NHS-biotin, Pierce Chemical Co., Rockford, Illinois, USA) and the manufacturer’s recommended conditions (450 μg NHS-biotin in 2.5 mL PBS-0.1 M HEPES per 150 mm2 plate, and then incubated for 45 minutes at room temperature). Cells were washed gently 3 times with cold PBS and then lysed in lysis buffer (10 mM Tris, 150 mM NaCl, 1.0 mM CaCl, 0.02% NaN3 2× protease inhibitor cocktail, and 2% Renex (Sigma Chemical Co.). Protein concentrations in the lysates were determined by bicinchoninic acid reaction (Pierce Chemical Co.), and equal amounts of total protein were immunoprecipitated.

Immunoprecipitation. Immunoprecipitation was carried out essentially as previously described (10). Lysates were precleared for 1 hour by incubation at 4°C with 100 μL γ-bind (Pharmacia Biotech AB, Uppsala, Sweden) in lysis buffer. After centrifugation, supernatants were collected and precleared with nonspecific Ab by the addition of 5 μg (5 μL) of hamster IgG (PharMingen, San Diego, California, USA) with 100 μL γ-bind and incubated for 1 hour at 4°C. After centrifugation, pellets were washed 4 times in 0.5 mL lysis buffer, and then finally resuspended in 75 μL gel loading buffer and boiled for 5 minutes before electrophoresis.

Blotting and detection. Western blots were carried out as described previously (11). Precipitated proteins were resolved by 8% SDS-PAGE. Proteins were electroblotted on nitrocellulose, and membranes were blocked in 10% skim milk, prepared in PBS with 0.05% Tween-20. Biotinylated proteins were detected by the addition of avidin–horseradish peroxidase conjugate (Pierce Chemical Co.), to 2 μg/mL in 10% milk, PBS, and 0.05% Tween-20 for 1 hour at room temperature. Membranes were washed extensively (5 times for 15 minutes) in PBS-0.05% Tween, and the blot was developed for horseradish peroxidase activity by enhanced chemiluminescence (ECL) (Amersham Life Sciences Inc., Arlington Heights, Illinois, USA).

Northern analysis. After Ficoll-Hypaque gradient purification, BMMs were cultured for 4 days in the presence of GM-CSF(10ng/mL), and an optimal amount of M-CSF (purified from L929 conditioned media) and recombinant GST-osteoprotegerin ligand (OPGL) (2 ng/mL) generated in our laboratory. Total RNA was isolated using Trizol (GIBCO BRL, Gaithersburg, Maryland, USA), and then analyzed using NorthernMax (Ambion Inc., Austin, Texas, USA). Nonisotopic probes were generated using the BrightStar kit (Ambion Inc.); GAPDH control probe was supplied by the manufacturer, murine β3 integrin probe consisted of a 537-nucleotide BamHI/HindIII fragment at the 5′ end of the cDNA (14), murine β5 integrin probe consisted of a 1-kb SalI fragment of cDNA (15).

Radiography. Four-month-old β3–/– mice were simultaneously radiographed with a β3+/+ or β3+/– littermate using mammography film.

Transmission electron microscopy. Long bones from 4- to 5-day-old β3+/– and β3–/– mice were dissected free of soft tissue and fixed with 2.5% glutaraldehyde and 4% paraformaldehyde in 0.01 M cacodylate buffer for at least 10 minutes. They were then washed and postfixed with 1% OsO4, dehydrated, and then embedded in araldite (Polyscience, Worhtington, Pennsylvania, USA). Sections were cut on an ultramicrotome and examined on an electron microscope (410; Philips Electron Optics, Mahwah, New Jersey, USA).

Examination of actin cytoskeleton. Long bones from 4- to 5-day-old mice were dissected free of soft tissue and sectioned longitudinally. They were placed in PBS in pyrocarbonate (DEPC)-treated water. Adherent marrow cells were removed with a fine paint brush. The bones were imprinted with minimal pressure onto salinated glass slides. The slides were air-dried at room temperature for 15 minutes, fixed with 3.7% formaldehyde, and then stained for TRAP by incubating with Naphthol AS-BI phosphate in the presence of 100 nM of sodium tartrate (osteoclasts were identified by expression of TRAP). To examine the F-actin distribution within osteoclasts, slides were treated with 0.1% Triton X-100 in PBS for 5 minutes and reacted with rhodamine phalloidin. A confocal microscope (MRC-1000; Bio-Rad Laboratories Inc., Hercules, California, USA) equipped with a PlanApo 60 × 1.4 NA objective was used to assess the cytoplasmic distribution of F-actin in TRAP-positive cells. The wavelength for excitation and emission for F-actin was 554 nm and 573 nm, respectively.

Bone resorption. Osteoclasts were generated in BMM/ST2 coculture on dentin slices for 7–10 days. Cells were removed from the dentin slices with 0.25 M ammonium hydroxide and mechanical agitation. Dentin slices were then subjected to scanning electron microscopy (16). Maximum resorption lacuna depth was measured using a confocal microscope (Microradiance; Bio-Rad Laboratories Inc.). Images were collected in 514-nm argon laser light with epireflection.

Results

β3–/– BMMs differentiate into osteoclasts that fail to spread. Similar to murine BMMs expressing the integrin subunit, osteoclasts can be generated from those that are β3 null (Figure 1). Within 7 days of coculture with the marrow stromal line, ST2, in the presence of 1,25-dihydroxyvitamin D3 and glucocorticoids, both wild-type and heterozygous BMMs differentiate into well spread, TRAP-expressing polykaryons (in all circumstances, β3+/+ and β3+/– BMMs yield similar results; thus, heterozygous or wild-type cells were utilized in various experiments on the basis of litter availability). β3-null macrophages also develop into numerous TRAP-positive multinucleated cells, but these fail to spread properly.

β3–/– BMMs differentiate into osteoclasts that fail to spread. Seven-day osFigure 1

β3–/– BMMs differentiate into osteoclasts that fail to spread. Seven-day osteoclastogenic cultures, containing BMMs of 2-month-old female littermates and ST2 stromal cells, were stained for TRAP activity (red reaction product). β3+/+ and β3+/– BMMs form numerous well spread, TRAP-expressing giant cells. TRAP-expressing cells in cultures with β3–/– BMMS, in contrast, fail to spread (×100). High magnification of the same cultures (bottom row) demonstrates that the TRAP-expressing giant cells, in each circumstance, contain multiple nuclei (arrow) (×250).

β3–/– BMMs fail to express αvβ3, and the integrin is not induced by IL-4. αvβ3 is minimally expressed by BMMs and appears as the cells assume the osteoclast phenotype (17) or are exposed to cytokines such as IL-4, which induces the integrin by transactivation of the β3 gene (10). To confirm that mutant BMMs lack the capacity to express αvβ3, we exposed β3+/– and β3–/– cells to IL-4 (50 units/mL) for 36 hours (10). The cells were surfaced labeled and lysed. The lysate was immunoprecipitated with a β3-specific antibody, and the immunoprecipitate was analyzed by SDS-PAGE. As expected, untreated heterozygous and mutant BMMs fail to express αvβ3 (Figure 2). Whereas the integrin is abundantly induced in cytokine-exposed heterozygous cells, αvβ3 remains undetectable in β3 knockout BMMs even in the presence of IL-4.

β3–/– BMMs fail to express αvβ3 and the integrin is not induced by IL-4. PuFigure 2

β3–/– BMMs fail to express αvβ3 and the integrin is not induced by IL-4. Pure populations of β3+/– or β3–/– BMMs were treated for 48 hours with vehicle (C) or murine IL-4 in an amount (5 ng/mL) known to optimally enhance β3 expression (10). The cells were then surface labeled with NHS-biotin and lysed, and then the lysate was immunoprecipitated with hamster antimurine β3 mAb and the immunoprecipitate subjected to SDS-PAGE. Similar to wild-type BMMs (10), β3+/– cells express minimal αvβ3 and the integrin is upregulated by IL-4. In contrast, β3–/– BMMs fail to express αvβ3 in the presence or absence of IL-4.

The β5 integrin subunit does not compensate for absence of β3. Although they do not express αvβ3, immature osteoclast precursors express αvβ5, which, like αvβ3, recognizes the RGD amino acid motif (17). We have shown that as BMMs differentiate into mature osteoclasts in vitro, αvβ5 is replaced by αvβ3 (17). This observation raised the possibility that the absence of β3 integrin, in differentiating osteoclast precursors, might be compensated by persistence of αvβ5. To determine if this is the case, we took advantage of the capacity of GM-CSF to reciprocally modulate β5 and β3 integrin expression, by BMMs, in a manner mirroring osteoclastogenesis (17). In fact, GM-CSF prompts disappearance of β5 mRNA in mutant as well as heterozygous BMMs (Figure 3). Thus, αvβ5 does not substitute for αvβ3 when the latter is absent in cytokine-stimulated osteoclast precursors.

The β5 integrin subunit does not compensate for absence of β3 in GM-CSF–treFigure 3

The β5 integrin subunit does not compensate for absence of β3 in GM-CSF–treated β3–/– BMMs. Pure populations of β3+/– or β3–/– BMMs were treated for 48 or 72 hours with vehicle (–) or murine GM-CSF (+) in an amount (10 ng/mL) known to optimally suppress β5 mRNA expression by wild-type BMMs (17). Total RNA was isolated and subjected to Northern analysis using a murine β5 cDNA. The cytokine inhibits β5 mRNA expression equally in β3+/– and β3–/– BMMs.

We next asked if β3 mRNA is absent and the β5 message is enhanced in β3 knockout cells, in the context of authentic osteoclastogenesis. To this end, we used RANKL which, in the presence of M-CSF, prompts BMM differentiation into osteoclasts (1). Thus, β3+/+ and β3–/– BMMs were treated with M-CSF alone or M-CSF plus RANKL. After 4 days, RNA was probed by Northern blot analysis using murine β3 and β5 cDNAs. β5 mRNA is abundant in wild-type and mutant cells treated only with M-CSF and diminishes, in both strains, with addition of RANKL (Figure 4). As expected, β3 message is enhanced by RANKL in wild-type BMMs and fails to appear in similarly treated null cells. Thus, at least in vitro, αvβ5 does not compensate for lack of αvβ3 in β3–/– cells committed to osteoclast differentiation.

Compensatory upregulation of β5 integrin does not occur in β3–/– osteoclastFigure 4

Compensatory upregulation of β5 integrin does not occur in β3–/– osteoclasts. Wild-type (WT) and β3–/– BMMs were grown in the presence of M-CSF alone or in combination with OPGL for 4 days. Ten micrograms of total RNA was run in each lane for Northern analysis. The blot was probed first with a combination of β5 and GAPDH probes, then stripped and probed with β3. In WT cultures, OPGL upregulates expression of β3 and downregulates expression of β5. In β3–/– cultures, no β3 mRNA is seen, and the downregulation of β5 is equivalent to that seen in WT cultures.

β3–/– mice become osteosclerotic with age. The external appearance of β3-null and wild-type mice, at birth and throughout life, is similar. On the other hand, as β3–/– mice age, they become osteosclerotic. This increase in bone mass is radiographically evident by 4 months. At 6 months, radiographs of mutant tails invariably demonstrate increased bone density, and, by this means, we can reliably discriminate β3-null from wild-type and heterozygous mice, the latter being indistinguishable from the wild-type in all parameters examined (Figure 5).

β3–/– mice develop radiographic osteosclerosis. Tails of 3 6-month-old β3–/Figure 5

β3–/– mice develop radiographic osteosclerosis. Tails of 3 6-month-old β3–/– mice and their heterozygous or wild-type sex-matched littermates were radiographed simultaneously to avoid technical artifacts. The mutant, in all circumstances, shows enhanced bone density.

Confirming our radiographic observations, histologic sections of β3–/– bones reveal a markedly increased cortical and trabecular mass (Figure 6). On the other hand, the histologic hallmark of osteopetrosis, namely the persistence of cartilaginous bars, reflecting failure to resorb primary spongiosa (18), is not evident in β3–/– animals.

β3–/– mice develop histologic osteosclerosis. Distal femora of 2 sets of 6-Figure 6

β3–/– mice develop histologic osteosclerosis. Distal femora of 2 sets of 6-month-old, sex-matched, β3+/+, β3+/–, and β3–/– littermates. Note the marked increase in cortical and trabecular bone mass in β3–/– mice as compared with wild-type and heterozygotes, which are indistinguishable. (Hematoxylin and eosin stained; ×40).

Osteoclasts in β3-1-mice are increased in number but dysfunctional. Despite their increased bone mass, mutant mice contain 15.0 ± 3.6 (SD) osteoclasts/mm trabecular bone surface as compared with 4.2 ± 1.1 (SD) osteoclasts/mm trabecular bone surface in their heterozygous littermates (P < 0.001) (Figure 7). Thus, osteoclasts appear in β3-null mice in increased numbers. Nonetheless, the bones of these mice progressively become osteosclerotic, suggesting that osteoclasts lacking αvβ3 may be defective. Consistent with this posture, circulating Ca2+ of mutant mice (4.38 mg/dL ± 0.27 [SD]) is substantially lower (P < .005) than that of heterozygotes (4.72 mg/dL ± .07 mg/dL [SD]). Hence, despite the increased number of osteoclasts present in β3–/– mice, they do not appear to efficiently resorb bone.

β3–/– mice generate increased numbers of osteoclasts. Histologic sections oFigure 7

β3–/– mice generate increased numbers of osteoclasts. Histologic sections of distal femoral metaphysic of 2-month-old β3+/– and β3–/– littermates were stained for TRAP activity (red reaction product) to identify osteoclasts that are increased in the mutant (×250).

To further define the nature of the osteoclast resorptive defect in β3-null mice, we examined β3+/– and β3–/– bone by transmission electron microscopy. As seen in Figure 8, the osteoclast’s resorptive organelle, namely the ruffled membrane, is distinctly abnormal in mutant cells. In contrast to the normal thin villous appearance of heterozygous ruffled membranes, this structure in β3 knockout osteoclasts consists of thick, blunted projections. Because ruffled membrane formation requires osteoclast/bone contact (19), failure of mutant osteoclasts to normally generate this structure suggests that essential, matrix-derived signals are mediated via αvβ3.

Ruffled membrane formation in osteoclasts of β3–/– mice is abnormal. ElectrFigure 8

Ruffled membrane formation in osteoclasts of β3–/– mice is abnormal. Electron micrographs of osteoclasts resident in metaphyseal bone of β3+/– and β3–/– mice. The ruffled membranes of heterozygous osteoclasts are indistinguishable from wild-type, whereas those of each β3–/– osteoclast consists of thickened and blunted villous structures. Scale bar: l.0 μm.

Ruffled membrane formation is typically associated with reorganization of the actin cytoskeleton (19). Furthermore, we demonstrated above (Figure 1), that whereas β3–/– BMMs develop into TRAP-positive multinucleated cells — in contrast to wild-type and heterozygous osteoclasts — these mutant polykaryons fail to spread. Thus, αvβ3 is not required for differentiation of osteoclast precursors into TRAP-expressing, multinuclear cells, but instead regulates their spreading capacity, which is also a function of the actin cytoskeleton.

To examine actin organization, primary osteoclasts (directly prepared as imprints from neonatal mouse bones) were permeabilized, stained with rhodamine-phalloidin, and subjected to confocal microscopy. Whereas the cytoskeleton of heterozygous osteoclasts is organized in circular structures consisting of podosomes or actin rings, in every mutant polykaryon examined, actin rings fail to form and actin is diffusely distributed, in a punctate pattern, throughout the cytoplasm (Figure 9). Therefore, αvβ3 transmits matrix-derived signals that organize the osteoclast cytoskeleton.

Actin organization in β3–/– osteoclasts is abnormal. β3+/– and β3–/– marrowFigure 9

Actin organization in β3–/– osteoclasts is abnormal. β3+/– and β3–/– marrow was blotted onto slides. The cells were stained for TRAP activity, permeabilized, and then incubated with rhodamine-phalloidin. TRAP-expressing multinucleated cells were identified and f-actin was visualized by confocal microscopy. β3+/– osteoclasts develop a characteristic actin ring, whereas F-actin in β3 osteoclasts is diffusely distributed throughout the cytoplasm.

Finally, we turned to the nature of the resorptive defect observed in β3 knockout osteoclasts. To this end, we generated β3+/– and β3–/– osteoclasts from BMMs on whale dentin, and imaged the resulting lacunae by scanning electron microscopy. Heterozygous osteoclasts excavate numerous characteristic, well delineated resorptive “pits” on the dentin surface, whereas those produced by cells lacking αvβ3 are shallow and poorly defined (Figure 10). Specifically, the mean maximum depth of lacunae excavated by β3+/– osteoclasts is 12.9 μm ± 2.9 (SD), whereas that of pits generated by β3–/– osteoclasts is 8.0 μm ± 0.8 (SD) (P < 0.001). Thus, αvβ3 is not required to initiate osteoclastic bone resorption, but is essential for its optimal expression.

The resorptive capacity of β3–/– osteoclasts is defective. Osteoclasts wereFigure 10

The resorptive capacity of β3–/– osteoclasts is defective. Osteoclasts were generated by culturing β3+/– or β3–/– BMMs with ST2 cells on dentin. After 7 days, the cells were removed, and resorption lacuna visualized by scanning electron microscopy. Whereas β3+/– osteoclasts produce numerous, well defined resorption lacunae, those formed by β3–/– osteoclasts have indistinct borders and are shallow.

Discussion

The αv family of integrins are heterodimeric, transmembrane molecules that both anchor cells to and transmit signals from the extracellular matrix. In fact, β integrin subunits contain cytoplasmic domains that, upon matrix recognition, serve as a nidus for the attachment of cytoskeletal proteins and signaling molecules, thereby dictating cell shape and motility (20).

Net bone degradation may reflect either the mean resorptive capacity of the mature polykaryon and/or the rates at which osteoclasts differentiate and die. Given this complex scenario, there are many possibilities by which αvβ3 may regulate skeletal mass. We posited, for example, that the integrin heterodimer may merely serve as a matrix-anchoring molecule, or, alternatively, it may also transmit intracellular signals initiating the resorptive process (21). Evidence has subsequently appeared, however, confirming that osteoclast αvβ3 transmits extracellular signals leading to phosphorylation of key integrin-associated signaling proteins such as pyk2 (22). This information, although suggestive, does not prove that αvβ3-mediated matrix-derived signals regulate the osteoclast’s capacity to resorb bone.

To address these issues, we generated β3 knockout mice that, as expected, exhibit Glanzmann’s thrombasthenia (8). These mutants grow normally, and, by external examination, they are indistinguishable from their wild-type and heterozygous counterparts. Thus, lack of αvβ3 does not impact skeletal modeling or sculpting; this is an important consideration if inhibitors of the integrin are to be administered to osteopenic children.

Unlike previously reported in vitro (8) and in vivo (4) inhibitor studies implying αvβ3 occupancy is necessary for optimal osteoclastogenesis, β3–/– mice not only contain osteoclasts but do so in substantially increased numbers. Given the hypocalcemia extant in the mutant mice, hyperparathyroidism likely prompts exuberant osteoclastogenesis. A similar scenario holds true in osteopetrosis (23).

β3 osteoclasts are, however, morphologically and functionally abnormal. This dysfunction reflects failure to optimally organize the cytoskeleton upon matrix contact and is consistent with our suggestion that polarization of the cell’s proton pump to its resorptive microenvironment reflects intracellular signals originating by recognition of αvβ3 ligand (21). In this regard, failure to form normal ruffled membranes and the striking cytoskeletal abnormalities of αvβ3-deficient osteoclasts suggest that the integrin functions not merely as an anchoring molecule, but also transmits essential, matrix-derived, intraosteoclastic signals. Proof of this posture will require distinction of the events mediated by only ligand recognition from intracellular signals transmitted by the integrin.

The impaired resorption extant in various osteopetrotic mutant mouse strains may represent failure to recruit osteoclasts (24) or diminished activity of the terminal polykaryon (25). The abundance of osteoclasts in the β3–/– mouse, also occurring in other states of resorptive insufficiency, both murine (25) and human (18), establishes that the resorptive defect in this mutant arises from diminished bone degradation by the mature cell and not from arrested osteoclastogenesis. On the other hand, osteoclast recruitment, a process requiring cell-matrix attachment, is brisk in the absence of αvβ3. Thus, an attachment molecule other than αvβ3 must mediate matrix recognition by β3–/– osteoclast precursors sufficient to permit differentiation, but insufficient to sustain normal bone degradation.

Macrophages, upon isolation from marrow, contain abundant αvβ5 and little αvβ3 (17). With commitment to the osteoclast phenotype, the β5 subunit is progressively replaced by β3. This observation raised the possibility that upon β3 deletion, αvβ5 persists and is functionally redundant. Such is not the case as osteoclast differentiation of both wild-type and mutant BMMs is attended by loss of αvβ5. We find, however, that β3–/– osteoclasts detach in the presence of collagenase and spread on native collagen (not shown), suggesting — but not proving — that collagen may serve as an attachment substrate sufficient for osteoclast differentiation, whereas optimal resorption requires αvβ3.

In contrast with studies of the role of αvβ3 in angiogenesis, wherein results with inhibitors (6) and genetic ablation (7, 8) are not in agreement, most of our observations conform with inhibitor experiments (3, 4). On the other hand, the potent αvβ3 ligand, echistatin dampens osteoclast formation in vitro (5), and an RGD peptidomimetic decreases osteoclast number in vivo (4). Thus, the β3 knockout mouse permits us to conclude that, in physiological circumstances, αvβ3 is probably not essential for osteoclastogenesis.

Perhaps the most challenging aspect of the αvβ3 knockout mouse is the relatively late appearance of profound osteosclerosis. The ability of β3–/– osteoclasts to initiate resorptive lacunae on dentin (albeit suboptimal), taken with normal skeletal development, tooth eruption, and resorption of physeal cartilage suggests bone remodeling proceeds in the absence of αvβ3. The fact that osteoclasts derived from 4- to 8-week-old mutants are dysfunctional indicates that the resorptive defect is not one acquired with age, but is instead the cumulative manifestation of partial osteoclast arrest. Thus, a reasonable hypothesis holds that although osteoclasts are dysfunctional in αvβ3-deficient mice, deployment of a larger than normal number of these cells initially achieves a reasonable net resorptive rate. With time, however, β3-null osteoclasts eventually fail to keep pace with bone deposition and osteosclerosis ensues.

Maintenance of skeletal integrity requires its continued remodeling (26). Hence, complete arrest of bone resorption is an undesirable feature of a potential bone-sparing agent. The fact, therefore, that bone resorption is not completely arrested in β3-null animals buttresses αvβ3 inhibition as a potential antiosteoporosis strategy.

Acknowledgments

We thank G. Papodemitirou of the University of Western Australia for his help. This work was supported by grants from the National Institutes of Health (NIH) (AR42404 to F.P. Ross; DE05413, AR46523, and AR32788 to S.L. Teitelbaum; National Heart, Lung, and Blood Institute grant HL41484 to R.O. Hynes; NIH grant GM07200 to J. Lam; NIH grant AR08335 to K.P. McHugh); Shriners’ Hospital for Crippled Children (grant 8560 to S.L. Teitelbaum); Alpha Omega Alpha Medical Honor Society 1998 Student Research Fellowship (to J. Lam); and by the Howard Hughes Medical Institute. K. Hodivala-Dilke was a fellow of the Human Frontiers Science Program and the Dystrophic Epidermolysis Bullosa Research Association. R.O. Hynes is an investigator of the Howard Hughes Medical Institute.

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