Primary cilia mediate mechanosensing in bone cells by a calcium-independent mechanism

Primary cilia are sensory organelles that translate extracellular chemical and mechanical cues into cellular responses. Bone is an exquisitely mechanosensitive organ, and its homeostasis depends on the ability of bone cells to sense and respond to mechanical stimuli. One such stimulus is dynamic fluid flow, which triggers biochemical and transcriptional changes in bone cells by an unknown mechanism. Here we report that bone cells possess primary cilia that project from the cell surface and deflect during fluid flow and that these primary cilia are required for osteogenic and bone resorptive responses to dynamic fluid flow. We also show that, unlike in kidney cells, primary cilia in bone translate fluid flow into cellular responses in bone cells independently of Ca2+ flux and stretch-activated ion channels. These results suggest that primary cilia might regulate homeostasis in diverse tissues by allowing mechanical signals to alter cellular activity via tissue-specific pathways. Our identification of a mechanism for mechanotransduction in bone could lead to therapeutic approaches for combating bone loss due to osteoporosis and disuse.

[1]  E. A. Tonna,et al.  Electron microscopy of aging skeletal cells. I. Centrioles and solitary cilia. , 1972, Journal of gerontology.

[2]  L. McIntire,et al.  Response of cultured endothelial cells to steady flow. , 1984, Microvascular research.

[3]  C. Dewey Effects of fluid flow on living vascular cells. , 1984, Journal of biomechanical engineering.

[4]  R M Nerem,et al.  The elongation and orientation of cultured endothelial cells in response to shear stress. , 1985, Journal of biomechanical engineering.

[5]  G. Piperno,et al.  Microtubules containing acetylated alpha-tubulin in mammalian cells in culture , 1987, The Journal of cell biology.

[6]  A Kamiya,et al.  The effect of fluid shear stress on the migration and proliferation of cultured endothelial cells. , 1986, Microvascular research.

[7]  G. Gawdi,et al.  Chloral hydrate disrupts mitosis by increasing intracellular free calcium. , 1987, Journal of cell science.

[8]  A Kamiya,et al.  A disk-type apparatus for applying fluid shear stress on cultured endothelial cell. , 1988, Biorheology.

[9]  C. Rieder,et al.  Flexible-substratum technique for viewing cells from the side: some in vivo properties of primary (9+0) cilia in cultured kidney epithelia. , 1988, Journal of cell science.

[10]  A. Kamiya,et al.  Increase in endothelial cell density before artery enlargement in flow-loaded canine carotid artery. , 1989, Arteriosclerosis.

[11]  R. Nerem,et al.  The Influence of Shear Stress on Cultured Vascular Endothelial Cells: The Stress Response of an Anchorage‐Dependent Mammalian Cell , 1989 .

[12]  J. Ando,et al.  Fluid shear stress enhanced DNA synthesis in cultured endothelial cells during repair of mechanical denudation. , 1990, Biorheology.

[13]  S. Ljunghall,et al.  Thrombin increases cytoplasmic Ca2+ and stimulates formation of prostaglandin E2 in the osteoblastic cell line MC3T3-El. , 1991, Bone and mineral.

[14]  Siep Thomas,et al.  THE POLYCYSTIC KIDNEY-DISEASE-1 GENE ENCODES A 14-KB TRANSCRIPT AND LIES WITHIN A DUPLICATED REGION ON CHROMOSOME-16 , 1994 .

[15]  P. Davies,et al.  Flow-mediated endothelial mechanotransduction. , 1995, Physiological reviews.

[16]  J. Tarbell,et al.  Modeling interstitial flow in an artery wall allows estimation of wall shear stress on smooth muscle cells. , 1995, Journal of biomechanical engineering.

[17]  R. Lorentzon,et al.  In situ microdialysis in bone tissue. Stimulation of prostaglandin E2 release by weight-bearing mechanical loading. , 1996, The Journal of clinical investigation.

[18]  D N Wheatley,et al.  EXPRESSION OF PRIMARY CILIA IN MAMMALIAN CELLS , 1996, Cell biology international.

[19]  E. Dejana,et al.  Targeted null-mutation in the vascular endothelial-cadherin gene impairs the organization of vascular-like structures in embryoid bodies. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[20]  Takayuki Asahara,et al.  Isolation of Putative Progenitor Endothelial Cells for Angiogenesis , 1997, Science.

[21]  J. Kearney,et al.  AC133, a novel marker for human hematopoietic stem and progenitor cells. , 1997, Blood.

[22]  H. Schatten,et al.  Chloral hydrate alters the organization of the ciliary basal apparatus and cell organelles in sea urchin embryos , 1998, Cell and Tissue Research.

[23]  D. Grant,et al.  VE-Cadherin mediates endothelial cell capillary tube formation in fibrin and collagen gels. , 1998, Experimental cell research.

[24]  J. Ando,et al.  Fluid shear stress increases the production of granulocyte-macrophage colony-stimulating factor by endothelial cells via mRNA stabilization. , 1998, Circulation research.

[25]  B L Langille,et al.  Transient and steady-state effects of shear stress on endothelial cell adherens junctions. , 1999, Circulation research.

[26]  Shu Chien,et al.  Mechanotransduction in Response to Shear Stress , 1999, The Journal of Biological Chemistry.

[27]  J. Isner,et al.  Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization. , 1999, Circulation research.

[28]  S. Schulz,et al.  Selective targeting of somatostatin receptor 3 to neuronal cilia , 1999, Neuroscience.

[29]  J. Isner,et al.  VEGF contributes to postnatal neovascularization by mobilizing bone marrow‐derived endothelial progenitor cells , 1999, The EMBO journal.

[30]  M. Gerritsen,et al.  Functional roles for PECAM-1 (CD31) and VE-cadherin (CD144) in tube assembly and lumen formation in three-dimensional collagen gels. , 1999, The American journal of pathology.

[31]  R Langer,et al.  Functional arteries grown in vitro. , 1999, Science.

[32]  N. Udagawa,et al.  A novel molecular mechanism modulating osteoclast differentiation and function. , 1999, Bone.

[33]  P. Carmeliet,et al.  Targeted Deficiency or Cytosolic Truncation of the VE-cadherin Gene in Mice Impairs VEGF-Mediated Endothelial Survival and Angiogenesis , 1999, Cell.

[34]  Haruchika Masuda,et al.  Ischemia- and cytokine-induced mobilization of bone marrow-derived endothelial progenitor cells for neovascularization , 1999, Nature Medicine.

[35]  N. Sato,et al.  Reciprocal gene expression of osteoclastogenesis inhibitory factor and osteoclast differentiation factor regulates osteoclast formation. , 1999, Biochemical and biophysical research communications.

[36]  K. Pantel,et al.  In vitro differentiation of endothelial cells from AC133-positive progenitor cells , 2000 .

[37]  C. Jacobs,et al.  Functional Gap Junctions Between Osteocytic and Osteoblastic Cells , 2000, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[38]  F. C. Lucibello,et al.  Endothelial-like cells derived from human CD14 positive monocytes. , 2000, Differentiation; research in biological diversity.

[39]  P. Niederer,et al.  A finite difference model of load-induced fluid displacements within bone under mechanical loading. , 2000, Medical engineering & physics.

[40]  T. Sasaguri,et al.  Laminar shear stress inhibits vascular endothelial cell proliferation by inducing cyclin-dependent kinase inhibitor p21(Sdi1/Cip1/Waf1) , 2000, Circulation research.

[41]  S. Rafii,et al.  Expression of VEGFR-2 and AC133 by circulating human CD34(+) cells identifies a population of functional endothelial precursors. , 2000, Blood.

[42]  J. Isner,et al.  Transplantation of ex vivo expanded endothelial progenitor cells for therapeutic neovascularization. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[43]  J. Isner,et al.  Vascular endothelial growth factor(165) gene transfer augments circulating endothelial progenitor cells in human subjects. , 2000, Circulation research.

[44]  S. Rafii,et al.  Circulating endothelial precursors: mystery, reality, and promise. , 2000, The Journal of clinical investigation.

[45]  R. Hebbel,et al.  Origins of circulating endothelial cells and endothelial outgrowth from blood. , 2000, The Journal of clinical investigation.

[46]  T. Murohara,et al.  Transplanted cord blood-derived endothelial precursor cells augment postnatal neovascularization. , 2000, The Journal of clinical investigation.

[47]  S. Rafii,et al.  Vascular Endothelial Growth Factor and Angiopoietin-1 Stimulate Postnatal Hematopoiesis by Recruitment of Vasculogenic and Hematopoietic Stem Cells , 2001, The Journal of experimental medicine.

[48]  S. Rafii,et al.  Impaired recruitment of bone-marrow–derived endothelial and hematopoietic precursor cells blocks tumor angiogenesis and growth , 2001, Nature Medicine.

[49]  H J Donahue,et al.  Osteopontin Gene Regulation by Oscillatory Fluid Flow via Intracellular Calcium Mobilization and Activation of Mitogen-activated Protein Kinase in MC3T3–E1 Osteoblasts* , 2001, The Journal of Biological Chemistry.

[50]  K. R. Spring,et al.  Bending the MDCK Cell Primary Cilium Increases Intracellular Calcium , 2001, The Journal of Membrane Biology.

[51]  R. Hartley,et al.  CD34− Blood‐Derived Human Endothelial Cell Progenitors , 2001, Stem cells.

[52]  S. Rafii,et al.  Mobilization of Endothelial and Hematopoietic Stem and Progenitor Cells by Adenovector‐Mediated Elevation of Serum Levels of SDF‐1, VEGF, and Angiopoietin‐1 , 2001, Annals of the New York Academy of Sciences.

[53]  L. Bonewald,et al.  Printed in U.S.A. Copyright © 2001 by The Endocrine Society PGE 2 Is Essential for Gap Junction-Mediated Intercellular Communication between Osteocyte-Like MLO-Y4 Cells in Response to Mechanical Strain , 2022 .

[54]  S. Homma,et al.  Neovascularization of ischemic myocardium by human bone-marrow–derived angioblasts prevents cardiomyocyte apoptosis, reduces remodeling and improves cardiac function , 2001, Nature Medicine.

[55]  A. Luttun,et al.  The Emerging Role of the Bone Marrow-Derived Stem Cells in (Therapeutic) Angiogenesis , 2001, Thrombosis and Haemostasis.

[56]  A. M. Simon,et al.  Cyclo‐Oxygenase 2 Function Is Essential for Bone Fracture Healing , 2002, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[57]  L. Bonewald,et al.  MLO‐Y4 Osteocyte‐Like Cells Support Osteoclast Formation and Activation , 2002, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[58]  Origin of endothelial progenitors in human postnatal bone marrow , 2002 .

[59]  R. Kuriyama,et al.  Characterization of Cep135, a novel coiled-coil centrosomal protein involved in microtubule organization in mammalian cells , 2002, The Journal of cell biology.

[60]  Christopher R Jacobs,et al.  Fluid flow induced PGE2 release by bone cells is reduced by glycocalyx degradation whereas calcium signals are not. , 2003, Biorheology.

[61]  K. Spring,et al.  Removal of the MDCK Cell Primary Cilium Abolishes Flow Sensing , 2003, The Journal of Membrane Biology.

[62]  M. Wong,et al.  Cyclic tensile strain and cyclic hydrostatic pressure differentially regulate expression of hypertrophic markers in primary chondrocytes. , 2003, Bone.

[63]  Focal adhesion kinase expression during mandibular distraction osteogenesis: evidence for mechanotransduction. , 2003 .

[64]  T. Murohara,et al.  Hypoxic Preconditioning Augments Efficacy of Human Endothelial Progenitor Cells for Therapeutic Neovascularization , 2003, Laboratory Investigation.

[65]  Christie M. Orschell,et al.  Peripheral Blood “Endothelial Progenitor Cells” Are Derived From Monocyte/Macrophages and Secrete Angiogenic Growth Factors , 2003, Circulation.

[66]  Jing Zhou,et al.  Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells , 2003, Nature Genetics.

[67]  J. Whitfield Primary cilium—is it an osteocyte's strain‐sensing flowmeter? , 2003, Journal of cellular biochemistry.

[68]  Kimiko Yamamoto,et al.  Proliferation, differentiation, and tube formation by endothelial progenitor cells in response to shear stress. , 2003, Journal of applied physiology.

[69]  L. Goldstein,et al.  Kidney-specific inactivation of the KIF3A subunit of kinesin-II inhibits renal ciliogenesis and produces polycystic kidney disease , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[70]  T. Stearns,et al.  Centrosome number is controlled by a centrosome-intrinsic block to reduplication , 2003, Nature Cell Biology.

[71]  S. Rafii,et al.  Molecular pathways regulating mobilization of marrow-derived stem cells for tissue revascularization. , 2003, Trends in molecular medicine.

[72]  J. Frøkiaer,et al.  Bending the Primary Cilium Opens Ca2+-sensitive Intermediate-Conductance K+ Channels in MDCK Cells , 2003, The Journal of Membrane Biology.

[73]  C. Jacobs,et al.  Fluid flow-induced prostaglandin E2 response of osteoblastic ROS 17/2.8 cells is gap junction-mediated and independent of cytosolic calcium. , 2003, Bone.

[74]  Y. Yoon,et al.  Intramyocardial Transplantation of Autologous Endothelial Progenitor Cells for Therapeutic Neovascularization of Myocardial Ischemia , 2003, Circulation.

[75]  Millie Hughes-Fulford,et al.  Signal Transduction and Mechanical Stress , 2004, Science's STKE.

[76]  S. Ponik,et al.  Formation of focal adhesions on fibronectin promotes fluid shear stress induction of COX-2 and PGE2 release in MC3T3-E1 osteoblasts. , 2004, Journal of applied physiology.

[77]  G. Pazour Intraflagellar transport and cilia-dependent renal disease: the ciliary hypothesis of polycystic kidney disease. , 2004, Journal of the American Society of Nephrology : JASN.

[78]  Richard T. Lee,et al.  Cell mechanics and mechanotransduction: pathways, probes, and physiology. , 2004, American journal of physiology. Cell physiology.

[79]  I. Vorobjev,et al.  Vertebrate primary cilia: a sensory part of centrosomal complex in tissue cells, but a “sleeping beauty” in cultured cells? , 2004, Cell biology international.

[80]  W. Marshall,et al.  De Novo Formation of Left–Right Asymmetry by Posterior Tilt of Nodal Cilia , 2005, PLoS biology.

[81]  K. Anderson,et al.  Cilia and Hedgehog responsiveness in the mouse. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[82]  S. Christakos,et al.  The Vitamin D Receptor, Runx2, and the Notch Signaling Pathway Cooperate in the Transcriptional Regulation of Osteopontin* , 2005, Journal of Biological Chemistry.

[83]  Sheldon Weinbaum,et al.  In situ measurement of solute transport in the bone lacunar‐canalicular system , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[84]  Katarina T. Borer,et al.  Physical Activity in the Prevention and Amelioration of Osteoporosis in Women , 2005, Sports medicine.

[85]  Peter Satir,et al.  PDGFRαα Signaling Is Regulated through the Primary Cilium in Fibroblasts , 2005, Current Biology.

[86]  G. Germino,et al.  Polycystin 2 Interacts with Type I Inositol 1,4,5-Trisphosphate Receptor to Modulate Intracellular Ca2+ Signaling* , 2005, Journal of Biological Chemistry.

[87]  Shiqin Zhang,et al.  Cilia-like Structures and Polycystin-1 in Osteoblasts/Osteocytes and Associated Abnormalities in Skeletogenesis and Runx2 Expression* , 2006, Journal of Biological Chemistry.

[88]  I. Stokes,et al.  Endochondral growth in growth plates of three species at two anatomical locations modulated by mechanical compression and tension , 2006, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[89]  T. Weimbs,et al.  Polycystin-1, STAT6, and P100 function in a pathway that transduces ciliary mechanosensation and is activated in polycystic kidney disease. , 2006, Developmental cell.

[90]  Nicholas F LaRusso,et al.  Cholangiocyte cilia detect changes in luminal fluid flow and transmit them into intracellular Ca2+ and cAMP signaling. , 2006, Gastroenterology.

[91]  C. Jacobs,et al.  Oscillatory fluid flow-induced shear stress decreases osteoclastogenesis through RANKL and OPG signaling. , 2006, Bone.

[92]  L. Guay-Woodford,et al.  Loss of primary cilia results in deregulated and unabated apical calcium entry in ARPKD collecting duct cells. , 2006, American journal of physiology. Renal physiology.

[93]  G. Pazour,et al.  The intraflagellar transport protein IFT20 is associated with the Golgi complex and is required for cilia assembly. , 2006, Molecular biology of the cell.

[94]  F. Grosveld,et al.  Atherosclerotic Lesion Size and Vulnerability Are Determined by Patterns of Fluid Shear Stress , 2006, Circulation.

[95]  J. Reiter,et al.  The Primary Cilium as the Cell's Antenna: Signaling at a Sensory Organelle , 2006, Science.

[96]  G. Walz,et al.  Polycystic kidney disease: cell division without a c(l)ue? , 2006, Kidney international.

[97]  W. Jackson,et al.  Intraflagellar transport is essential for endochondral bone formation , 2007, Development.