Rabbit tendon cells produce MMP-3 in response to fluid flow without significant calcium transients.

Forces applied to tendon during movement cause cellular deformation, as well as fluid movement. The goal of this study was to test the hypothesis that rabbit tendon fibroblasts detect and respond to fluid-induced shear stress. Cells were isolated from the paratenon of the rabbit Achilles tendon and then subjected to fluid flow at 1 dyn/cm(2) for 6h in a specially designed multi-slide flow device. The application of fluid flow led to an increased expression of the collagenase-1 (MMP-1), stromelysin-1 (MMP-3), cyclooxygenase II (COX-2) and interleukin-1beta (IL-1beta) genes. The release of proMMP-3 into the medium exhibited a dose-response with the level of fluid shear stress. However, not all cells aligned in the direction of flow. In other experiments, the same cells were incubated with the calcium-reactive dye FURA-2 AM, then subjected to laminar fluid flow in a parallel plate flow chamber. The cells did not significantly increase intracellular calcium concentration when exposed to fluid shear stress levels of up to 25 dyn/cm(2). These results show that gene expression in rabbit tendon cells is sensitive to fluid flow, but that signal transduction is not dependent on intracellular calcium transients. The upregulation of the MMP-1, MMP-3 and COX-2 genes shows that fluid flow could be an important mechanical stimulus for tendon remodelling or injury.

[1]  M. Klagsbrun,et al.  AP-1 mediates stretch-induced expression of HB-EGF in bladder smooth muscle cells. , 1999, American journal of physiology. Cell physiology.

[2]  R L Duncan,et al.  Ca(2+) regulates fluid shear-induced cytoskeletal reorganization and gene expression in osteoblasts. , 2000, American journal of physiology. Cell physiology.

[3]  S. Jern,et al.  Effects of shear stress on eicosanoid gene expression and metabolite production in vascular endothelium as studied in a novel biomechanical perfusion model. , 2000, Biochemical and biophysical research communications.

[4]  L. Dahners,et al.  Cell populations of tendon: A simplified method for isolation of synovial cells and internal fibroblasts: Confirmation of origin and biologic properties , 1988, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[5]  Musculoskeletal,et al.  Sports-Induced Inflammation: Clinical and Basic Science Concepts , 1990 .

[6]  V. Mow,et al.  Mitogen-activated protein kinase signaling in bovine articular chondrocytes in response to fluid flow does not require calcium mobilization. , 2000, Journal of biomechanics.

[7]  W Herzog,et al.  Response of Rabbit Achilles Tendon to Chronic Repetitive Loading , 2001, Connective tissue research.

[8]  S. Chien,et al.  Biomechanical regulation of matrix metalloproteinase‐9 in cultured chondrocytes , 2000, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[9]  J A Frangos,et al.  Effect of flow on prostaglandin E2 and inositol trisphosphate levels in osteoblasts. , 1991, The American journal of physiology.

[10]  P C Amadio,et al.  Method for the measurement of friction between tendon and pulley , 1995, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[11]  K. O. Mercurius,et al.  Stimulation of transcription factors NF kappa B and AP1 in endothelial cells subjected to shear stress. , 1994, Biochemical and biophysical research communications.

[12]  J. Ralphs,et al.  Tendons and ligaments--an overview. , 1997, Histology and histopathology.

[13]  L. S. Matthews,et al.  Analysis of cumulative strain in tendons and tendon sheaths. , 1987, Journal of biomechanics.

[14]  S. Izumo,et al.  Control of endothelial cell gene expression by flow. , 1995, Journal of biomechanics.

[15]  C. Hung,et al.  Real‐Time Calcium Response of Cultured Bone Cells to Fluid Flow , 1995, Clinical orthopaedics and related research.

[16]  W. Smutz,et al.  Investigation of low-force high-frequency activities on the development of carpal-tunnel syndrome. , 1994, Clinical biomechanics.

[17]  C. Hung,et al.  Intracellular calcium response of ACL and MCL ligament fibroblasts to fluid-induced shear stress. , 1997, Cellular signalling.

[18]  C. Jacobs,et al.  Effects of fluid flow on intracellular calcium in bovine articular chondrocytes. , 1997, The American journal of physiology.

[19]  M. Muda,et al.  Calcium signalling and gene expression. , 1999, Journal of receptor and signal transduction research.

[20]  D. Hart,et al.  Pregnancy induces complex changes in the the pattern of mRNA expression in knee ligaments of the adolescent rabbit. , 1998, Matrix biology : journal of the International Society for Matrix Biology.

[21]  A. Charles,et al.  Mechanical stimulation and intercellular communication increases intracellular Ca2+ in epithelial cells. , 1990, Cell regulation.

[22]  J. Frangos,et al.  Fluid shear stress stimulates prostaglandin and nitric oxide release in bone marrow-derived preosteoclast-like cells. , 2000, Biochemical and biophysical research communications.

[23]  Y. Iwamoto,et al.  Fluid Shear Stress Increases Transforming Growth Factor Beta 1 Expression in Human Osteoblast-like Cells: Modulation by Cation Channel Blockades , 1998, Calcified Tissue International.

[24]  R Wells,et al.  Quantifying exposure in occupational manual tasks with cumulative trauma disorder potential. , 1991, Ergonomics.

[25]  A. Banes,et al.  Mechanoreception at the cellular level: the detection, interpretation, and diversity of responses to mechanical signals. , 1995, Biochemistry and cell biology = Biochimie et biologie cellulaire.

[26]  D. Bozentka,et al.  The effect of shear stress on fibroblasts derived from Dupuytren's tissue and normal palmar fascia. , 1998, The Journal of hand surgery.

[27]  T. Peterson,et al.  Protein kinases as mediators of fluid shear stress stimulated signal transduction in endothelial cells: a hypothesis for calcium-dependent and calcium-independent events activated by flow. , 1995, Journal of biomechanics.

[28]  D. Burr,et al.  Fluid shear-induced mechanical signaling in MC3T3-E1 osteoblasts requires cytoskeleton-integrin interactions. , 1998, American journal of physiology. Cell physiology.