Intracellular tension in periosteum/perichondrium cells regulates long bone growth

Perichondrium/periosteum is involved in regulating long bone growth. Long bones grow faster after removal or circumferential division of periosteum. This can be countered by culturing them in conditioned medium from perichondrium/periosteum cells. Because both complete removal and circumferential division are effective, we hypothesized that perichondrium/periosteum cells require an intact environment to release the appropriate soluble factors. More specifically, we propose that this release depends on their ability to generate intracellular tension. This hypothesis was explored by modulating the ability of perichondrium/periosteum cells to generate intracellular tension and monitoring the effect thereof on long bone growth. Perichondrium/periosteum cells were cultured on substrates with different stiffness. The medium produced by these cultures was added to embryonic chick tibiotarsi from which perichondrium/periosteum was either stripped or left intact. After 3 culture days, long bone growth was proportionally related to the stiffness of the substrate on which perichondrium/periosteum cells were grown while they produced conditioned medium. A second set of experiments demonstrated that the effect occurred through expression of a growth‐inhibiting factor, rather than through the reduction of a stimulatory factor. Finally, evidence for the importance of intracellular tension was obtained by showing that the inhibitory effect was abolished when perichondrium/periosteum cells were treated with cytochalasin D, which disrupts the actin microfilaments. Thus, we concluded that modulation of long bone growth occurs through release of soluble inhibitors by perichondrium/periosteum cells, and that the ability of cells to develop intracellular tension through their actin microfilaments is at the base of this mechano‐regulated control pathway. © 2010 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 29:84–91, 2011

[1]  E Bell,et al.  Production of a tissue-like structure by contraction of collagen lattices by human fibroblasts of different proliferative potential in vitro. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[2]  M. Dembo,et al.  Substrate flexibility regulates growth and apoptosis of normal but not transformed cells. , 2000, American journal of physiology. Cell physiology.

[3]  R. Goss,et al.  Regulation of Organ and Tissue Growth , 1971, Science.

[4]  Karin Macfelda,et al.  Behavior of cardiomyocytes and skeletal muscle cells on different extracellular matrix components--relevance for cardiac tissue engineering. , 2007, Artificial organs.

[5]  Viktor Hamburger,et al.  A series of normal stages in the development of the chick embryo , 1992, Journal of morphology.

[6]  A. Hodgson,et al.  Physiologic leg lengthening. A preliminary report. , 1970, Clinical orthopaedics and related research.

[7]  M. Bissell,et al.  Modulation of secreted proteins of mouse mammary epithelial cells by the collagenous substrata , 1984, The Journal of cell biology.

[8]  J E Bertram,et al.  Mechanics of avian fibrous periosteum: tensile and adhesion properties during growth. , 1998, Bone.

[9]  F. Grinnell,et al.  Studies on the mechanism of hydrated collagen gel reorganization by human skin fibroblasts. , 1985, Journal of cell science.

[10]  C. Oomens,et al.  The non-linear mechanical properties of soft engineered biological tissues determined by finite spherical indentation , 2008, Computer methods in biomechanics and biomedical engineering.

[11]  Y. Wang,et al.  Cell locomotion and focal adhesions are regulated by substrate flexibility. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[12]  Rik Huiskes,et al.  Collagen orientation in periosteum and perichondrium is aligned with preferential directions of tissue growth , 2008, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[13]  F. Long,et al.  Regulation of growth region cartilage proliferation and differentiation by perichondrium. , 1998, Development.

[14]  Rik Huiskes,et al.  Residual periosteum tension is insufficient to directly modulate bone growth. , 2009, Journal of biomechanics.

[15]  Dennis Discher,et al.  Substrate compliance versus ligand density in cell on gel responses. , 2004, Biophysical journal.

[16]  Chang Kp,et al.  8 Physiologic Leg Lengthening A Preliminary Report , 1970 .

[17]  D. Jenkins,et al.  Stimulation of bone growth by periosteal stripping. A clinical study. , 1975, The Journal of bone and joint surgery. British volume.

[18]  Christopher S. Chen Mechanotransduction – a field pulling together? , 2008, Journal of Cell Science.

[19]  M. Dembo,et al.  Cell movement is guided by the rigidity of the substrate. , 2000, Biophysical journal.

[20]  F. Long,et al.  Regulation of endochondral cartilage growth in the developing avian limb: cooperative involvement of perichondrium and periosteum. , 2001, Developmental biology.

[21]  C. Hartmann,et al.  Dual roles of Wnt signaling during chondrogenesis in the chicken limb. , 2000, Development.

[22]  David J Odde,et al.  Traction Dynamics of Filopodia on Compliant Substrates , 2008, Science.

[23]  P. Janmey,et al.  Effects of substrate stiffness on cell morphology, cytoskeletal structure, and adhesion. , 2005, Cell motility and the cytoskeleton.

[24]  F. Grinnell,et al.  Contraction of hydrated collagen gels by fibroblasts: evidence for two mechanisms by which collagen fibrils are stabilized. , 1987, Collagen and related research.

[25]  V. Hamburger,et al.  A series of normal stages in the development of the chick embryo. 1951. , 2012, Developmental dynamics : an official publication of the American Association of Anatomists.

[26]  S. Sen,et al.  Matrix Elasticity Directs Stem Cell Lineage Specification , 2006, Cell.

[27]  G. Gabbiani Faculty Opinions recommendation of Focal adhesion size controls tension-dependent recruitment of alpha-smooth muscle actin to stress fibers. , 2006 .

[28]  M. Crochiere,et al.  Multiple mechanisms of perichondrial regulation of cartilage growth , 2002, Developmental dynamics : an official publication of the American Association of Anatomists.

[29]  D. Lovitch,et al.  Mineralization is more reliable in periosteum explants from size-selected chicken embryos , 1997, In Vitro Cellular & Developmental Biology - Animal.

[30]  M. Grounds,et al.  Extracellular matrix, growth factors, genetics: their influence on cell proliferation and myotube formation in primary cultures of adult mouse skeletal muscle. , 1995, Experimental cell research.

[31]  Jean-Jacques Meister,et al.  Focal adhesion size controls tension-dependent recruitment of α-smooth muscle actin to stress fibers , 2006, The Journal of cell biology.

[32]  M. Moss CHAPTER 7 – THE REGULATION OF SKELETAL GROWTH , 1972 .

[33]  Clifford J. Tabin,et al.  Regulation of Rate of Cartilage Differentiation by Indian Hedgehog and PTH-Related Protein , 1996, Science.

[34]  G. C. Baker,et al.  Circumferential periosteal release in the treatment of children with leg-length inequality. , 1987, The Journal of bone and joint surgery. British volume.

[35]  Ben Fabry,et al.  Single-cell response to stiffness exhibits muscle-like behavior , 2009, Proceedings of the National Academy of Sciences.

[36]  F. Baaijens,et al.  Essential environmental cues from the satellite cell niche: optimizing proliferation and differentiation. , 2009, American journal of physiology. Cell physiology.

[37]  E. Hay,et al.  Analysis of the role of microfilaments and microtubules in acquisition of bipolarity and elongation of fibroblasts in hydrated collagen gels , 1984, The Journal of cell biology.

[38]  Marion Ghibaudo,et al.  Rigidity-driven growth and migration of epithelial cells on microstructured anisotropic substrates , 2007, Proceedings of the National Academy of Sciences.

[39]  P. Janmey,et al.  Tissue Cells Feel and Respond to the Stiffness of Their Substrate , 2005, Science.

[40]  R. Serra,et al.  The perichondrium plays an important role in mediating the effects of TGF‐β1 on endochondral bone formation , 2001, Developmental dynamics : an official publication of the American Association of Anatomists.

[41]  Ulrich S Schwarz,et al.  Physical determinants of cell organization in soft media. , 2005, Medical engineering & physics.