Leucine-rich repeat kinase 1 (LRRK1) plays a critical role in regulating cytoskeletal organization, osteoclast activity, and bone resorption with little effect on bone formation parameters. Deficiency of Lrrk1 in mice causes a severe osteopetrosis in the metaphysis of the long bones and vertebrae bones, which makes LRRK1 an attractive alternative drug target for the treatment of osteoporosis and other high-turnover bone diseases. This review summarizes recent advances on the functions of the Lrrk1-related family members, Lrrk1 deficiency-induced skeletal phenotypes, LRRK1 structure–function, potential biological substrates and interacting proteins, and the mechanisms of LRRK1 action in osteoclasts.
Osteoporosis, a common age-related disorder, occurs as a consequence of two major causes:1 low peak bone mineral density (BMD), which is typically achieved at ~age 30 years, and2 a high bone loss rate, which normally occurs after menopause and during the natural process of aging. Bone loss occurs with age partly when the bone resorption rate is greater than the bone formation rate. Although bone resorption is coupled with bone formation during normal physiological conditions to maintain bone homeostasis, an increased number and/or function of osteoclasts are known to contribute to excessive bone loss during disease states and aging. The processes of bone formation and bone resorption are regulated by systemic hormones, nutrition, local growth factors, and mechanical stimuli.1,2 A high-throughput screen aimed at the identification of the functions of over 4 500 genes led to the discovery of a leucine-rich repeat kinase 1 (LRRK1) as a critical regulator of osteoclast function and bone resorption with little effect on bone formation.3,4 The severe osteopetrosis phenotype in long and axial bones observed in Lrrk1 knockout (KO) mice makes LRRK1 an ideal drug target for the prevention and treatment of osteoporotic fractures. This review summarizes recent advances on the functions of the Lrrk1-related family members, Lrrk1 deficiency-induced skeletal phenotypes, LRRK1 structure–functional, potential biological substrates and interacting proteins, and the mechanisms of LRRK1 action in osteoclasts.
LRRK1 family numbers
LRRK1 belongs to the ROCO family of proteins that are characterized by their unique domains including leucine-rich repeats (LRRs) and/or ankyrin repeats (ANK), a GTPase-like domain of ras of complex proteins (ROC), a C terminus of Roc domain (COR) with an unknown function, a serine/threonine kinase domain that shares sequence similarity with MAPKKK (mitogen-activated protein kinase kinase kinase), and a series of WD40 repeats in their C termini.5,
MASL1, also known as malignant fibrous histiocytoma-amplified sequence 1, is the only ROCO protein lacking a kinase domain.7,
DAPK1 contains a death domain on its C terminus and a kinase domain on its N terminus, but lacks the LRR repeats.14 Examination of the DAPK1 kinase domain revealed that DAPK1 is a Ca2+/calmodulin-dependent kinase linked with the cytoskeleton and a mediator of apoptosis.15 Inhibition of DAPK1 expression suppressed apoptosis, whereas the overexpression of DAPK1 resulted in neuronal cell death.16,
LRRK2 is one of the most studied proteins among the ROCO family proteins. Mutations in Lrrk2 have been associated with autosomal-dominant Parkinson’s disease (PD), a neurodegenerative disorder with symptoms of resting tremor, postural instability, muscle rigidity, and bradykinesia.25,26 The Lrrk2 gene encodes a large multi-domain protein of 2 527 amino acids. A mutation of G2019S in the kinase domain of LRRK2 has been shown to elevate its kinase activity, GTP binding, and contributed to PD, whereas other mutations identified in patients with PD had no effect on the kinase activity.27,
The human Lrrk1 gene is located on chromosome 15 (15q26.3) and consists of 34 exons spanning a region of over 150 kb. The coding region of the Lrrk1 mRNA encodes a protein of 2 015 amino acids with an estimated molecular weight of 250 kDa.38 It is believed that Lrrk1 and Lrrk2 in vertebrates may be derived from the same ancient gene by DNA duplication.38 Though LRRK1 and LRRK2 share similar structures, including the presence of LRR, and a ROC–COR domain, a serine/threonine kinase, and WD40 repeats, only LRRK1 has ankyrin-like repeats in its N terminus.39,40 Lrrk1was first identified as a mammalian growth regulatory factor in U2OS osteosarcoma cells, and the overexpression of Lrrk1 in human HEK293 cells was found to induce cell proliferation.41 However, loss of Lrrk1 in mice caused severe osteopetrosis.3 Lrrk1−/− mice were born alive, with the expected Mendelian frequency at 2 weeks of age. The body length of the Lrrk1 KO mice was slightly shorter compared to the wild-type (WT) control littermates at 4 weeks of age. Targeted disruption of Lrrk1 resulted in the highest observed body volumetric bone mineral density (vBMD) of the 3 629 distinct gene KO lines examined by dual-energy x-ray absorptiometry (DEXA) using high-throughput screening.3 The vBMD of Lrrk1 KO mice was higher than Sost and c-Src KO mice. Both Lrrk1 KO males and females have the same elevation in total BMD as compared to WT gender-matched littermate mice, and the increase in BMD in the long bones and spines of KO mice was persistent during aging. Micro computed tomography (micro-CT) analyses revealed that the trabecular bone volume was markedly increased in 8-week old, growing Lrrk1 KO mice, as well as, in 79-week-old aging mice due to elevated trabecular number and trabecular thickness, and reduced trabecular separation. Interestingly, long bones had a wider metaphysis, normal diaphysis, but reduced marrow cavity area. Disruption of Lrrk1 also resulted in slightly increased cortical bone thickness in the tibia and femur shaft in young as well as aging mice due to reduced endocortical resorption as total area (diameter) was unaffected and the marrow cavity area was reduced. In contrast to markedly elevated trabecular bone volume in long bones and vertebrae, our unpublished data showed that deficiency of Lrrk1 had only a mild effect on the skull. The calvarias from Lrrk1 KO mice had normal total volume (TV) but 20% higher BV and 17% higher BV/TV than control mice (Figure 1). In the mandible, TV, bone volume (BV), and BV/TV in Lrrk1 KO mice were increased 25%, 34%, and 7%, respectively. The modest skull and mandible phenotypes of Lrrk1 KO mice compared to the long bones and the vertebra are consistent with evidence that regulation of osteoclast function is different in membranous and endochondral bone, or that the osteoclast-mediated bone remodeling is less relevant in flat bones compared to long bones or vertebrae.
Histological analyses showed that there was extensive unresorbed cartilage below the growth plate of the distal femur and proximal tibia of Lrrk1 KO mice, and numerous tartrate-resistant acid phosphatase (TRAP)-positive osteoclasts with an increased trabecular number and trabecular bone volume. The primary spongiosa in the Lrrk1 KO mice extended to the diaphysis and was characterized by increased mature osteoclasts, cartilage, and trabecular bone. The secondary spongiosa was very short and incomplete. The Lrrk1 KO osteoclasts in bone contained increased amounts of pale eosinophilic cytoplasm with enlarged scattered nuclei. Histological examinations of teeth and surrounding bones at 79 weeks of age found that Lrrk1 KO mice had normal incisors, molars, and periodontal ligaments. The turbinate bones were of normal thickness and contained prominent basophilic (reversal) lines. Consistent with the micro-CT analyses, there was modest osteosclerosis of the periodontal bone, nasal septum, and bridge of the nose. Analyses of serum chemistry values from Lrrk1 KO and WT control littermates showed that TRAP5b, a marker of osteoclast number, was elevated both in young and older mice.
More recently, an autosomal recessive mutation of Lrrk1 has been identified in a human patient.42 A partial DNA deletion in the Lrrk1 gene caused a frame-shift mutation, resulting in the disruption of the 7th WD40 repeats, and addition of a 66-amino-acid sequence to the C terminus of the LRRK1 protein. The mutation caused a loss of LRRK1 function in osteoclasts. The clinical features of the patient were very similar to the skeletal phenotypes observed in the Lrrk1 KO mice. The patient with a loss of function mutation had an osteosclerotic metaphyseal dysplasia, a distinctive form of osteopetrosis characterized by severe osteosclerosis confined to the metaphysis of the long and short tubular bones due to osteoclast dysfunction.3,42 A skeletal survey showed a normal skull; the vertebral bodies were of normal height but had mild marginal sclerosis. The ribs were slightly broad. Marginal sclerosis of the ilia and broad, and sclerotic metaphyses of the proximal femur were noted. Hand radiographs showed broad, sclerotic metaphyses of the distal radius and ulna, and sclerotic metaphyses of the metacarpals and phalanges. The skeletal phenotypes in Lrrk1 KO mice and the clinical skeletal signs in the affected patient with an Lrrk1 gene mutation are summarized in Table 1. The human genetic studies together with the studies in the Lrrk1 KO mouse model strongly suggest that LRRK1 plays a critical role in regulating osteoclast function and peak bone mass.
Lrrk1 and Lrrk2 expression
Drosophila and lower vertebrate organisms such as Fugu and Zebrafish have only a single Lrrk gene, whereas the mammalian genome contains both Lrrk1 and Lrrk2 genes.40 Biskup et al recently measured Lrrk1 and Lrrk2 mRNA in multiple organs in neonatal and adult mice, and found that expression levels of Lrrk1 and Lrrk2 mRNA were almost identical in the lung, heart, skeletal muscle, and lymph node.43 However, Lrrk2 mRNA is more abundant in kidney and brain tissue, whereas Lrrk1 mRNA is more abundant in the stomach, liver, small intestine, thymus, and smooth muscle. Other studies indicated that Lrrk2 mRNA is expressed in adult rat striatum, hippocampus, cerebral cortex, sensory and sympathetic ganglia, lung, spleen, and kidney.44 In the developing rat striatum, Lrrk2 transcription is first observed at postnatal day 8, followed by increased levels of expression up to 3 weeks of age. The expression level then remains constant for nearly 2 years. The time course of postnatal development of Lrrk2 expression patterns in the striatum thus closely mirrors the postnatal development of dopamine innervation of the striatum. Lrrk1 is also found in most tissues of the postnatal day 1 rats. It is also known to be expressed in a number of adult rat tissues including brain, adrenal gland, liver, lung, spleen, and kidney. Interestingly, although both Lrrk1 and Lrrk2 are expressed in the adult human cortex cerebra, hippocampus, only Lrrk2, but not Lrrk1, is expressed in the striatum.44,45 Strong expression of Lrrk2 is mainly found in neurons, specifically in the dopamine receptor 1 (DRD1a) and 2 (DRD2)-positive subpopulations of the striatal medium spiny neurons.45 More recently, Lrrk1 expression is found to be low in murine osteoblasts and osteocytes, but its expression is significantly increased during the late stages of osteoclast differentiation.42 These studies strongly suggest that the two paralogous family members may not have overlapping functions, although they have partly complementary expression patterns in the brain, as well as in certain peripheral organs including lymphatic tissues and bones. The differential expression patterns of Lrrk1 and Lrrk2 genes in specific cell types and developmental stages may explain in part why loss of Lrrk1 exhibited skeletal phenotypes but not PD, and Lrrk2 expression could not compensate for the loss of Lrrk1 in bones.3
Functional domains of Lrrk1 in osteoclasts
The large multi-domains of LRRK1 could function as an adapter, a kinase, or a GTPase-modulating protein of focal adhesion molecules in osteoclasts. Previous studies have linked mutations in the Lrrk2 but not the Lrrk1 gene in humans to PD, although both Lrrk1 and Lrrk2 are expressed in multiple tissues including macrophage precursors.25,40,43,46,47 Although both LRRK1 and LRRK2 have several common functional motifs, LRRK1 but not LRRK2 contains N-terminal ANK repeats.39,40 Sequence analysis found that LRRK1 contains four ANK repeats that are highly identical to the ANK repeat consensus sequence. The predicted three-dimensional structure of the ANK repeat domain of human LRRK1 is similar to secondary structures of the typical ANK repeats and the Ankyrin repeat, SH3-domain, and proline-rich-region containing protein 2 (ASPP2, also known as 53BP2), which binds to p53 as a co-activator and regulates cell apoptosis.48 It contains functional motifs of β-hairpins, inner helices, and outer helices that can bind to important proteins involved in podosome assembly and disassembly in osteoclasts (Figures 2a and b).48,
Previous findings indicate that the K651A point mutation of the ROC region of LRRK1 prevents GTP binding, reduces enzymatic activity, and impairs osteoclast bone resorption.54,
Mechanisms of Lrrk1 action in osteoclasts
The ability of the mature osteoclasts to resorb bone is largely regulated by cytoskeletal organization, and its function is dependent on actin ring or sealing zone formation. By using primary osteoclast precursors derived from WT and Lrrk1 KO mice, recent in vitro osteoclast differentiation and resorptive pit formation studies revealed that Lrrk1-deficient monocytes can differentiate into larger, TRAP-positive multinuclear osteoclasts. Interestingly, most of the Lrrk1-deficient mature osteoclasts showed diffused F-actin or small actin rings in the cytoplasm, and they failed to form one large peripheral F-actin ring, and assemble sealing rings when seeded on bone slices. These flat cells remained on the bone surface, but were not associated with resorption pits, a similar phenotype also found in Wiskott–Aldrich syndrome protein (WASP)-deficient cells.60 Only a very small portion (<5%) of the Lrrk1 KO osteoclasts exhibited typical but extremely large, round, and weak peripheral rings.3 This study indicates that dysfunction of Lrrk1-deficient osteoclasts contributes to the disruption of cytoskeletal rearrangement, as well as sealing ring and podosome assembly in osteoclasts.
Potential substrates of LRRK1 kinase
Very little is known about the direct biological substrates in osteoclasts, and the mechanism underlying regulation of LRRK1 on osteoclast function. Kedashiro et al reported that LRRK1 regulates epidermal growth factor receptor (EGFR) trafficking by phosphorylating mouse CLIP-170 (also named as CLIP1) at threonine residue 1 384 within the waTnc motif. This promotes the association of CLIP-170 with dynein–dynactin complex formation, and the subsequent recruitment of p150Glued to microtubule plus ends in HEK293 human kidney cells.61,62 Although changes in EGFR activation are known to influence osteoclast formation and survival,63 loss of Lrrk1 in the precursors did not affect osteoclast formation and maturation. Mice with complete disruption of EGFR function exhibited a remarkable decrease in tibial trabecular bone mass with abnormalities in trabecular number and thickness due to the decreases in osteoblast number and mineralization activity, and an increase in osteoclast number.64 Thus, it is unlikely that an interaction of LRRK1 with EGFR will play a critical role in regulating osteoclast activity and bone mass. Though CLIP-170 is involved in cytoskeleton arrangement, male mice with disruption of CLIP-170 exhibited abnormal sperm and reduced fertility without skeletal phenotypes,65 whereas Lrrk1-deficient males showed normal fertility but severe osteopetrosis.3 A nonsense mutation in the human CLIP-170 gene caused the absence of CLIP-170 transcripts and protein, resulting in an autosomal recessive intellectual disability without radiographically detectable skeletal abnormalities66 (and personal communication). Recently, Barrera et al reported that LRRK1 phosphorylates DCK5RAP2 in its γ-tubulin-binding motif to promote the interaction of CDK5RAP2 with γ-tubulin. LRRK1 phosphorylation of human CDK5RAP2 at serine 140 (ggSei) is necessary for the mitotic spindle orientation.67 However, mice with the loss of CDK5RAP2 function exhibited small size, kyphosis, severe anemia, and neonatal death, which are not consistent with the phenotypes of Lrrk1 KO mice that we observed.3,68,69 The peptide sequences of potential LRRK1 substrates from the two reports appear to lack conserved substrate motifs, and this is inconsistent with a predicted phosphor-PKCs’ substrate motif.70 Therefore, neither CLIP-170 nor CDK5RAP2 is likely a key biological substrate of LRRK1 in osteoclasts.
The ability of mature osteoclasts to resorb bone is largely dependent on cytoskeletal organization or sealing zone formation. The integrin αvβ3, c-Src, and Rac are key regulators of the osteoclast cytoskeleton and osteoclast activity, but do not promote osteoclastogenesis.71,
It is known that Csk, a nonreceptor tyrosine kinase, negatively regulates c-Src activity by phosphorylating Tyr-527 and switching the c-Src from the active open formation to an inactive closed architecture.81,82 There is evidence that Csk is recruited to the membrane where c-Src is in an active state through binding to Csk-binding protein.83,84 Mice with disruption of Csk caused embryonic lethality because of developmental arrest.85 However, overexpression of Csk in osteoclasts caused disorganization of the cytoskeleton, and strongly suppressed resorptive pit formation in vitro, whereas overexpression of kinase inactive, dominant negative Csk in osteoclasts caused increased c-Src activity, and bone-resorbing activity in vitro and in vivo assays.86 These observations strongly support the prediction that LRRK1 may modulate c-Src signaling pathways via interacting with Csk and modifying its function in osteoclasts.
Sun et al87 reported that a serine residue within the catalytic domain of Csk was phosphorylated and inactivated by the c-AMP-dependent protein kinase A in vitro. In addition, other studies also reported that protein kinase A phosphorylated Csk at serine residues and as a result inactivated Csk in the acrosome and flagellum of murine spermatozoa.88 Although serine 364 phosphorylation of Csk is associated with Csk auto-phosphorylation and activation in T cells,89 the function of serine/threonine phosphorylation in osteoclasts, and whether Csk kinase activity in Lrrk1 KO osteoclasts is reduced remain unknown, and need to be further studied.
Although previous studies from our group have shown that LRRK1 plays a critical role in regulating osteoclast sealing zone formation, osteoclast activity, and bone resorption due to altered Tyr-527 phosphorylation of c-Src,3 mice with Lrrk1 disruption exhibit a more severe osteopetrosis phenotype than c-Src KO mice, suggesting that LRRK1 signaling may target other signaling molecules besides the Csk/Chk/c-Src signaling pathway via post-translational modification.3 Several signaling pathways including integrin, nuclear factor kappa-B (NF-kB), and Src could be involved in regulating osteoclast function.90 Rac1/cdc42 are small guanosine triphosphatases (GTPases), which belong to the RAS superfamily of small GTP-binding proteins and are known to regulate a wide range of cellular activities, including the control of cell growth, cytoskeletal reorganization, and the activation of protein kinases. Studies have showed that double KO of Rac1 and Rac2 in mice caused severe metaphyseal osteopetrosis due to cytoskeleton disarrangement and osteoclast dysfunction.73,74 Although Rac1/2-deficient osteoclasts in vitro and Rac1/2 KO mice exhibited bone resorption defects, the magnitude of phenotypic changes caused by lack of Rac1/2 is less severe than that of Lrrk1-deficient cells or Lrrk1 KO mice. Histomorphometric parameters of osteoblasts in Lrrk1 KO mice were similar to the adult RAC1/RAC2 KO mice. Both KO strains exhibited reduced osteoblast function and bone formation in vivo but the cell mineralization in vitro was normal, suggesting that the in vivo defect in osteoblast activity was not cell intrinsic. In addition, mice with deletion of Rac1/2 in mature osteoclasts also had a normal response to PTH treatment, just as in the case of Lrrk1 KO mice.74,91 Furthermore, RAC1 has been reported to interact with LRRK2 protein.92 These studies strongly suggest that small GTPase Rac1/Cdc42 may be direct biological substrates of LRRK1. Our recent studies have revealed that Lrrk1 deficiency in osteoclasts resulted in reduced phosphorylation and activation of RAC1/Cdc42. In vitro kinase assays confirmed that LRRK1 phosphorylated RAC1-GST, and immunoprecipitation analyses found that the interaction of LRRK1 with RAC1 occurred after RANKL treatment. Overexpression of constitutively active Q61L RAC1 partially rescued the resorptive function of Lrrk1-deficient osteoclasts. Further studies revealed that the lack of Lrrk1 in osteoclasts led to reduced PAK1 auto-phosphorylation, catalyzed by RAC1/Cdc42 binding and activation. Interestingly, RAC1 and Cdc42 proteins bear consensus substrate motifs (RxRxxS) for PKCs and protein kinases with motifs similar to PKCs.93 In supporting these studies, Cdc42-deficient and Cdc42 downstream WASP KO mice also showed severe osteopetrosis phenotypes.60,94 Osteoclasts lacking WASP spread over a much larger surface area and are highly polykaryotic. WASP-null cells were depleted of podosomes, and failed to form actin rings at sealing zones, a phenotype similar to what Lrrk1-null cells exhibited.54,60 Based on these studies, it is likely that LRRK1 may regulate osteoclast function via modulation of phosphorylation and activation of small GTPase RAC1/Cdc42 proteins and RAC1/Cdc42 proteins may be a part of direct biological substrates of LRRK1 in osteoclasts.54
Potential binding partners of LRRK1 kinase
Multiple domains of LRRK1 could also play a role as a scaffold in mediating protein–protein interactions. Recent findings have demonstrated the importance of TBC1D2-dependent Rab7 inactivation in LRRK1 regulation of autophagy formation in mouse embryo fibroblasts.95 Mice with disruption of Lrrk1 were vulnerable to starvation and disrupted autolysosome formation due to a defect in lysosomal degradation during autophagy and reduced conversion of Rab7-GTP to GDP resulted from a reduction in the Rab7 GTPase-activating protein activity of TBC1D2. Indeed, Rab7, Rac1, and other Ras-like small GTPase proteins appear to act in concert to modulate ruffled border formation of bone-resorbing osteoclasts via protein–protein interactions and co-localization.73,74,96,
More recently, it has been demonstrated that LRRK1 regulates B-cell development and activation via positively modulating CARMA1 (caspase recruitment domain, CARD, membrane-associated guanylate kinase, MAGUK, protein 1) scaffold function to activate the NF-kB cascade in B lymphocytes.103 B cells lacking Lrrk1 exhibited a profound defect in proliferation and survival upon BCR stimulation, and had impaired BCR-mediated NF-kB activation and NF-kB target gene expression. The NF-kB has been shown to regulate positively osteoclast differentiation, and negatively modulate osteoblast differentiation.104,105 Although mice lacking NF-kB exhibited osteopetrosis due to an increase in bone resorption and bone formation in vivo, the phenotypic changes of osteoclasts lacking NF-kB in vitro were inconsistent with the osteoclast cultures derived from Lrrk1 KO mice, ruling out involvement of NF-kB signaling in LRRK1 regulation of osteoclast function.106
In our previous studies, we have demonstrated that LRRK1 physically interacts with Csk in osteoclasts in vitro.3 Besides potential serine/threonine phosphorylation and inactivation of Csk, there is also a possibility that LRRK1 interacts with Csk, leading to a Csk conformation change and inactivation. In addition, interaction of LRRK1 with Csk may alter Csk membrane localization, causing reduced Csk binding to Csk-binding protein/PAG1 on the lipid rafts where c-Src is localized. Thus, we can assume that in the presence of LRRK1, Csk is on a leash, thus c-Src Y527 is not phosphorylated and the osteoclast is active. In the absence of LRRK1, active Csk phosphorylates c-Src Y527 causing c-Src inactivation and osteoclast dysfunction.
Topologic structure of LRRK1 and LRRK2 functional domains
It has been difficult to resolve the crystal structure of LRRK2 because either full-length recombinant proteins or truncated proteins expressed in Escherichia coli are insoluble, unstable, or permanently bound to chaperones.39 Because the kinase domain is well conserved in the ROCO family of proteins across species, and ROCO4 has a sequence similarity of 47% to LRRK2, Gilsbach et al107 recently expressed the Dictyostelium ROCO4 kinase WT domain and corresponding PD-related mutant domains in E. coli, and resolved the structures of the ROCO4 kinase domain with LRRK2 inhibitor H1152. In the absence of crystal structure of the kinase domain of LRRK1 and LRRK2, the crystallography of the ROCO4 kinase domain can be used as a template for homology modeling of the LRRK2 or LRRK1 kinase domain for structure-based drug screening and structure refining.59 The crystal structure of the ROC domain dimer from LRRK2 has also been resolved and was used for a combination of computer-aided drug design for screening small-molecule competitors against the GTP pocket for treatment of PD.39,108 Little is known about the structures of LRRK1 kinase or ROC domains. Blast searches to identify suitable templates for modeling of the human LRRK1 kinase domain have led to three highly significant matches. The detected templates of transforming growth factor-beta-activated kinase 1 (TAK1), constitutive triple response 1 kinase, and mixed-lineage kinase 1 all belong to the PKC-like superfamily of serine/threonine protein kinases, and have been co-crystallized with small inhibitors.109,
Model for LRRK1 mechanism of action in osteoclasts
Recent studies suggest that there is an extensive cross-talk between integrin, c-Src, and Rho signaling pathways.90 The osteopetrosis phenotype in Lrrk1 KO mice are much more severe than the c-Src KO, integrin beta 3 KO, or RAC1/2 double KO mice, although these mice display partially overlapping skeletal abnormalities that are caused by defective bone remodeling and dysfunctional osteoclasts. Although integrin, Src, and Rac1 are predicted to localize in the same signaling pathway, these molecules are also regulated by multiple upstream growth factors, protein kinases, and protein phosphatases. Inactivation of only the Src/Rac1 pathway by Lrrk1 deficiency could not explain the severe phenotypes observed in Lrrk1 KO mice. It is, therefore, possible that LRRK1 modulates other signaling pathways besides c-Src and Rac1/Cdc42. On the basis of current publications, we propose a model of the mechanism of LRRK1 action in osteoclasts as shown in Figure 3. In this model, phosphorylation and activation of LRRK1 by membrane receptors may regulate cytoskeletal arrangement, podosome assembly, and osteoclast activity via modulating multiple signaling pathways that are also triggered by a number of extracellular matrix proteins and growth factors such as the receptor for macrophage colony-stimulating factor, EGF, tumor necrosis factors, and RANKL (receptor activator of nuclear factor kappa-B ligand). Activation of integrin αvβ3, EGF, macrophage colony-stimulating factor receptor, and RANK stimulates Syk-mediated GTP binding to Rac1/Cdc42 via the phosphorylated Vav3 in osteoclasts, activate downstream factors, and promote cytoskeletal rearrangement. Integrin αvβ3 and RANK also control small GTPase-mediated regulation of the cytoskeletal remodeling proteins WASP that is crucial for podosome formation and osteoclast polarization.60,116 Although LRRK1 could directly mediate phosphorylation and activation of Rac1/cdc42 and CLIP1, it could also indirectly modulate c-Src phosphorylation via inactivating Csk, and Rab7-GDP vs Rab7-GTP conversion through TBC1D2 (tubulin-specific chaperone cofactor C1 domain family member 2), stimulating ruffled border and podosome formation. Although membrane receptors can activate NF-kB signaling pathways via TAK1/IKKs, inducing osteoclast differentiation, there is no evidence that LRRK1 influences osteoclast formation through activating IKK/NF-kB signaling pathway.
Conclusions and future directions
There is now considerable evidence to demonstrate that LRRK1 plays a key role in regulating cytoskeletal organization and osteoclast activity. Deficiency of Lrrk1 in mice causes a much higher BMD in the long bones and vertebrae than any other gene KO mouse lines that have been tested, which makes LRRK1 an attractive alternative drug target for the treatment of osteoporosis and osteoporotic fractures.4 The potential substrates in osteoclasts could be Csk, CLIP1, and Rac1/Cdc42 small GTPases. However, there are a number of other issues that remain to be addressed including: (1) are there other biological substrates in osteoclasts besides Csk, CLIP1, and Rac1/Cdc42? (2) Does LRRK1 regulate functions in other cell types such as chondrocyte differentiation and hypotrophy besides osteoclast function? (3) What are the upstream activators of LRRK1 and how is LRRK1 activated? (4) How does the LRRK1 signaling pathway interact with other known signaling pathways involved in the regulation of cytoskeletal rearrangement? (5) What is the three-dimensional crystal structure of the LRRK1 kinase domain? (6) What is structural difference between the full-length WT human LRRK1 and WD40 mutant human LRRK1 and does WD40 mutation affect the kinase conformation and activation? More information about these questions will facilitate the structure-based drug design for small molecular weight inhibitors and optimize the therapeutic strategies for prevention and treatment of osteoporosis.
We thank Dr Donna Strong for her proofreading. This research was supported by National Institutes of Health grant AR066831-01 and ASBMR GAP grant to Weirong R Xing. The funder had no role in study design, data collection and analysis, decision to publish, or manuscript preparation. The salary SM was supported by a senior research career scientist award from the Department of Veteran’s Affairs. The research work was performed at facilities provided by the Department of Veterans Affairs.
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