The osteocyte as a wiring transmission system.

The mechanism of transduction of mechanical strains into biological signals remains one of the more baffling problems of skeletal homeostasis. The updated literature ascribes to osteocytes the function of sensing the strains induced into the bone matrix by mechanical stresses. Whether the osteocytes perform such function by themselves or they are helped by other cells is also unknown. Indeed TEM investigations carried out in our laboratory pointed out the existence of a functional syncytium among all the cells of the osteogenic lineage (COL; stromal cells, osteoblasts or bone lining cells, osteocytes). On the basis of this finding, we suggested that COL may reciprocally modulate their function not only by volume transmission (paracrine and autocrine stimulation) but also by wiring transmission, namely in a neuronal like manner. Thanks to their location, osteocytes should theoretically be the first cells of COL functional syncytium to sense mechanical strains, whereas stromal cells should be the first to be activated by hormonal molecules diffusing across the endothelial lining. Since PTH and Estrogen receptors have also been localized on osteocytes, and considering that such hormones have been suggested to modulate the sensitivity to strain of the bone mechanosensor, we suggested that the osteocyte syncytium may constitute the microscopic bone structure that sense both mechanical strain and biochemical factors and, at any moment, after having combined the two types of stimuli, issues the appropriate signals to the other bone cells by volume and/or wiring-transmission. Stromal cells, on the other hand, besides transmitting signals from vascular endothelium to bone cells, may control the differentiation and then direct the course of the osteoblasts around the vascular framework.

[1]  G. Marotti,et al.  ULTRASTRUCTURAL EVIDENCE OF THE EXISTENCE OF A DENDRITIC NETWORK THROUGHOUT THE CELLS OF THE OSTEOGENIC LINEAGE: THE NOVEL CONCEPT OF WIRING- AND VOLUME-TRANSMISSION IN BONE , 1996 .

[2]  Harold M. Frost,et al.  Bone "mass" and the "mechanostat" , 1987 .

[3]  D. Zaffe,et al.  Quantitative investigation on osteocyte canaliculi in human compact and spongy bone. , 1985, Bone.

[4]  N. Waters,et al.  Maturation Rate of the Osteon of the Cat , 1963, Nature.

[5]  G. Marotti The structure of bone tissues and the cellular control of their deposition. , 1996, Italian journal of anatomy and embryology = Archivio italiano di anatomia ed embriologia.

[6]  H. Frost Bone “mass” and the “mechanostat”: A proposal , 1987, The Anatomical record.

[7]  J M Polak,et al.  Mechanical Strain Stimulates Nitric Oxide Production by Rapid Activation of Endothelial Nitric Oxide Synthase in Osteocytes , 1999, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[8]  G. Marotti,et al.  Morphological study of intercellular junctions during osteocyte differentiation. , 1990, Bone.

[9]  G. Marotti,et al.  Osteocyte-Bone Lining Cell System at the Origin of Steady Ionic Current in Damaged Amphibian Bone , 1998, Calcified Tissue International.

[10]  G. Marotti,et al.  A quantitative evaluation of osteoblast-osteocyte relationships on growing endosteal surface of rabbit tibiae. , 1992, Bone.

[11]  A. Favia,et al.  Distribution of resorption processes in the compacta and spongiosa of bones from lactating rats fed a low-calcium diet. , 1988, Bone.

[12]  D. Zaffe,et al.  Osteocyte differentiation in the tibia of newborn rabbit: an ultrastructural study of the formation of cytoplasmic processes. , 1990, Acta anatomica.

[13]  C. Bagi,et al.  Comparison of osteopenic changes in cancellous bone induced by ovariectomy and/or immobilization in adult rats , 1994, The Anatomical record.

[14]  G. Marotti,et al.  Stromal cell structure and relationships in perimedullary spaces of chick embryo shaft bones , 1998, Anatomy and Embryology.