IL‐1β sensitizes intervertebral disc annulus cells to fluid‐induced shear stress

椎间盘 机械转化 剪应力 细胞生物学 化学 卡尔帕因 生物物理学 材料科学 解剖 医学 生物 生物化学 酶 复合材料
作者
Michelle K. Elfervig,Joe T. Minchew,Eric Francke,Mari Tsuzaki,Albert J. Banes
出处
期刊:Journal of Cellular Biochemistry [Wiley]
卷期号:82 (2): 290-298 被引量:53
标识
DOI:10.1002/jcb.1153
摘要

Abstract Chronic inflammation and altered mechanical loading are implicated as contributors to intervertebral disc degeneration. Biomechanical and biochemical factors play a role in disc degeneration but have received limited study. Mechanically, intervertebral discs are sheared during bending or twisting of the trunk. Biochemically, IL‐1β, detected in degenerative discs, promotes metalloproteinase expression. We hypothesized that disc cells might respond to shear stress and IL‐1β in a calcium signaling response. We measured the effect of single and combined stimuli on intracellular calcium concentration ([Ca 2+ ] ic ) and signaling. Cells were isolated from annulus tissue, cultured to quiescence, plated on collagen‐bonded Culture Slips ® and incubated with Fura‐2AM. Cells then were incubated in IL‐1β. Cell response to the effects of fluid flow was tested using FlexFlo™, a laminar flow device. Human annulus (hAN) cells responded to laminar fluid flow with a one to three‐fold increase in [Ca 2+ ] ic . IL‐1β alone produced a small, transient stimulation. hAN cells pretreated with IL‐1β responded to shear with a more dramatic and sustained increase in [Ca 2+ ] ic , six to ten‐fold over basal level, when compared to shear then IL‐1β or shear and IL‐1β alone ( P < 0.001 for all comparisons). This is the first study documenting synergism of a signaling response to biomechanical and biochemical stimuli in human disc cells. IL‐1β treatment appeared to “sensitize” annulus cells to mechanical load. This increased responsiveness to mechanical load in the face of inflammatory cytokines may imply that the sensitivity of annulus cells to shear increases during inflammation and may affect initiation and progression of disc degeneration. J. Cell. Biochem. 82: 290–298, 2001. © 2001 Wiley‐Liss, Inc.
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