The Three-Dimensional Morphometry and Cell–Cell Communication of the Osteocyte Network in Chick and Mouse Embryonic Calvaria

The study of osteocytes has progressed in chicks. We examined whether chick osteocyte data can be applied to other species. We used mice for comparison because they are common clinical tools in biomedical research and useful for future study. We analyzed the three-dimensional (3D) osteocyte network and gap junctional intercellular communication (GJIC) in living embryonic calvaria for the anatomical features. Embryonic parietal bones were stained with fluorescently labeled phalloidin and observed using confocal laser scanning microscopy. GJIC between osteocytes in chick and mouse parietal bone was assessed using fluorescence recovery after photobleaching (FRAP). The values for one chick and mouse osteocyte, respectively, were calculated as follows: cell processes 1,131 ± 139 μm, 2,668 ± 596 μm; surface area 1,128 ± 358 μm2, 2,654 ± 659 μm2; and cell volume 455 ± 90 μm3, 1,328 ± 210 μm3. The density of 3D osteocyte processes in the bone matrix was not significantly different. FRAP analysis showed dye coupling among osteocytes in chick and mouse bone. The fluorescence intensity recovered to 49.0 ± 2.4% in chicks and 39.9 ± 2.4% in mice after 5 minutes. Fluorescence recovery was similar within 4 minutes. The difference in osteocyte size between the two species might have affected their functions. Osteocyte processes in the two species may sense similarly changes in the exterior environment. We successfully conducted morphological and functional analyses of the osteocyte network in chicks and mice. The size of the osteocytes in bone differed between the two species.

[1]  A. van der Plas,et al.  Sensitivity of osteocytes to biomechanical stress in vitro , 1995, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[2]  H. Ris,et al.  Primary Cultures of Chick Osteocytes Retain Functional Gap Junctions between Osteocytes and between Osteocytes and Osteoblasts , 2007, Microscopy and Microanalysis.

[3]  L. Lanyon Osteocytes, strain detection, bone modeling and remodeling , 2005, Calcified Tissue International.

[4]  H. Sissons,et al.  Quantitative histology of osteocyte lacunae in normal human cortical bone , 1976, Calcified Tissue Research.

[5]  L. Qin,et al.  Histomorphological study on pattern of fluid movement in cortical bone in goats , 1999, The Anatomical record.

[6]  R Huiskes,et al.  Osteocyte density changes in aging and osteoporosis. , 1996, Bone.

[7]  S. Cowin,et al.  A model for the excitation of osteocytes by mechanical loading-induced bone fluid shear stresses. , 1994, Journal of biomechanics.

[8]  L. Lanyon,et al.  Early strain‐related changes in enzyme activity in osteocytes following bone loading in vivo , 1989, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[9]  T. Steinberg,et al.  Connexin43 Deficiency Causes Delayed Ossification, Craniofacial Abnormalities, and Osteoblast Dysfunction , 2000, The Journal of cell biology.

[10]  P. Nijweide,et al.  Signal transduction pathways involved in fluid flow-induced PGE2 production by cultured osteocytes. , 1999, The American journal of physiology.

[11]  Connexin 43 as a signaling platform for increasing the volume and spatial distribution of regenerated tissue , 2009, Proceedings of the National Academy of Sciences.

[12]  S. Cowin,et al.  Candidates for the mechanosensory system in bone. , 1991, Journal of biomechanical engineering.

[13]  D Vashishth,et al.  Determination of bone volume by osteocyte population , 2002, The Anatomical record.

[14]  P. Hughes,et al.  Ontogenetic and regional morphologic variations in the turkey ulna diaphysis: implications for functional adaptation of cortical bone. , 2003, The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology.

[15]  M. Ferretti,et al.  Histomorphometric study on the osteocyte lacuno-canalicular network in animals of different species. I. Woven-fibered and parallel-fibered bones. , 1998, Italian journal of anatomy and embryology = Archivio italiano di anatomia ed embriologia.

[16]  J. Skedros Osteocyte Lacuna Population Densities in Sheep, Elk and Horse Calcanei , 2006, Cells Tissues Organs.

[17]  S. Morony,et al.  OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph-node organogenesis , 1999, Nature.

[18]  S. Nishikawa,et al.  The murine mutation osteopetrosis is in the coding region of the macrophage colony stimulating factor gene , 1990, Nature.

[19]  B L Langille,et al.  Cardiac malformation in neonatal mice lacking connexin43. , 1995, Science.

[20]  J. Trosko,et al.  A fluorescence photobleaching assay of gap junction-mediated communication between human cells. , 1986, Science.

[21]  H. Ris,et al.  Osteocyte Shape Is Dependent on Actin Filaments and Osteocyte Processes Are Unique Actin‐Rich Projections , 1998, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[22]  Stephen C Cowin,et al.  Estimation of bone permeability using accurate microstructural measurements. , 2006, Journal of biomechanics.

[23]  C. Hernandez,et al.  Osteocyte density in woven bone. , 2004, Bone.

[24]  A. van der Plas,et al.  Isolation and purification of osteocytes , 1992, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[25]  R Huiskes,et al.  Osteocyte density and histomorphometric parameters in cancellous bone of the proximal femur in five mammalian species , 1996, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[26]  T. Takano-Yamamoto,et al.  A three-dimensional distribution of osteocyte processes revealed by the combination of confocal laser scanning microscopy and differential interference contrast microscopy. , 2001, Bone.

[27]  David Taylor,et al.  The role of osteocytes and bone microstructure in preventing osteoporotic fractures , 2006, Osteoporosis International.

[28]  L. Bonewald,et al.  Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism , 2006, Nature Genetics.

[29]  D. Rao,et al.  Relationships between osteocyte density and bone formation rate in human cancellous bone. , 2002, Bone.

[30]  Mark L. Johnson,et al.  Osteocytes, mechanosensing and Wnt signaling. , 2008, Bone.

[31]  M. Muglia,et al.  Histomorphometric study on the osteocyte lacuno-canalicular network in animals of different species. II. Parallel-fibered and lamellar bones. , 1999, Italian journal of anatomy and embryology = Archivio italiano di anatomia ed embriologia.

[32]  T. Takano-Yamamoto,et al.  Fluid Shear Stress Induces Less Calcium Response in a Single Primary Osteocyte Than in a Single Osteoblast: Implication of Different Focal Adhesion Formation , 2006, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[33]  D. Rao,et al.  Age and distance from the surface but not menopause reduce osteocyte density in human cancellous bone. , 2002, Bone.

[34]  Teruko Takano-Yamamoto,et al.  Three-dimensional reconstruction of chick calvarial osteocytes and their cell processes using confocal microscopy. , 2005, Bone.

[35]  Makoto Sato,et al.  Targeted Disruption of Cbfa1 Results in a Complete Lack of Bone Formation owing to Maturational Arrest of Osteoblasts , 1997, Cell.