4.6 Article

Strain-induced mechanotransduction through primary cilia, extracellular ATP, purinergic calcium signaling, and ERK1/2 transactivates CITED2 and downregulates MMP-1 and MMP-13 gene expression in chondrocytes

期刊

OSTEOARTHRITIS AND CARTILAGE
卷 24, 期 5, 页码 892-901

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ELSEVIER SCI LTD
DOI: 10.1016/j.joca.2015.11.015

关键词

Chondrocyte mechanotransduction; Primary cilia; Cyclic tensile strain

资金

  1. Directorate For Engineering
  2. Div Of Civil, Mechanical, & Manufact Inn [1333560] Funding Source: National Science Foundation
  3. NIAMS NIH HHS [R01AR050968] Funding Source: Medline

向作者/读者索取更多资源

Objective: To determine the strain-induced signaling pathways involved in regulating the transactivation of the transcription regulator Cbp/p300 Interacting Transactivator with ED-rich tail 2 (CITED2) and downstream targets in chondrocytes. Methods: Primary human chondrocytes or C28/I2 chondrocytic cells were subjected to various strain regimes. C57BL/6 mice were subjected to treadmill running. Loss-of-functionwas carried out using siRNA or inhibitors specific for targeted molecules. mRNA levels were assayed by RT-qPCR, and proteins by western blotting, immunofluorescence, and/or immunohistochemical staining. CITED2 promoter activity was assayed in chondrocytes using wild-type or mutant constructs. Results: Cyclic strain at 5%, 1 Hz induced CITED2 expression and suppressed expression of matrix metalloproteinase (MMP)-1 and -13 at the messenger RNA (mRNA) and protein levels in human chondrocytes. Abolishing primary cilia through knockdown of intraflagellar transport protein (IFT88) attenuated CITED2 gene expression and decreased protein levels. Similar effects were observed with inhibitors of extracellular adenosine triphosphate (ATP) or P2 purinergic receptors, or antagonists of Ca2+ signaling. Knockdown of IFT88 in articular chondrocytes in vivo diminished treadmill induced-CITED2 expression and upregulated MMPs. Knockdown of hypoxia-inducible factor (HIF) 1 alpha, specificity protein 1 (Sp1), or deletion of the shear stress response element (SSRE) in the CITED2 promoter limited cyclic strain-induced transactivation of CITED2. However, the strain induced-transactivation of CITED2 was abolished only on knockdown of HIF1 alpha, Sp1, and SSRE or by loss-of-function of IFT88 or extracellular-signal-regulated kinases (ERK) 1/2. Conclusions: CITED2 transactivation is a critical event in signaling generated by strain and transduced by primary cilia, extracellular ATP, P2 purinergic receptors, and Ca2+ signaling. Strain-induced CITED2 transactivation requires HIF1 alpha, Sp1, and an intact SSRE and leads to the downregulation of MMPs such as MMP-1 and MMP-13. (c) 2015 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.

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