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诱导人关节软骨细胞分泌非胰腺磷脂酶A2的释放

Induction of release of secretory nonpancreatic phospholipase A2 from human articular chondrocytes.

作者信息

Pruzanski W, Bogoch E, Katz A, Wloch M, Stefanski E, Grouix B, Sakotic G, Vadas P

机构信息

Inflammation Research Group, The Wellesley Hospital, University of Toronto, Canada.

出版信息

J Rheumatol. 1995 Nov;22(11):2114-9.

PMID:8596153
Abstract

OBJECTIVE

Secretory nonpancreatic phospholipase A2 (sPLA2) is a known inducer/promoter of the inflammatory process in the joints. It correlates with disease activity in adult and juvenile rheumatoid arthritis. Synovial fluids contain high concentrations of sPLA2. We discovered that human articular cartilage contains large quantities of sPLA2 and that culture chondrocytes constitutively synthesize and release sPLA2. To test the mechanism controlling the release of sPLA2, we exposed cultured human articular chondrocytes to cytokines and other agents, known to induce sPLA2 in other cells.

METHODS

Chondrocytes obtained from cartilage of normal appearance from rheumatoid and osteoarthritic joints, and from normal, neonatal joints were compared to rabbit articular chondrocytes. Radiolabeled Escherichia coli derived phospholipid assay and ELISA technique using monoclonal antibodies against recombinant human synovial type sPLA2 were employed. The cells were grown as monolayers as well as in alginate beads.

RESULTS

Human articular chondrocytes from both arthritic and neonatal joints released sPLA2 constitutively but could not be further stimulated with interleukin-1 beta (IL-1 beta), tumor necrosis factor alpha (TNF-alpha), IL-6, oncostatin M, lipopolysaccharide (LPS), or forskolin. Marked stimulation was observed when the cells were exposed to 8-bromo cyclic adenosine monophosphate (cAMP). Growing the cells as monolayers or in alginate beads did not change the results. In contrast to human cells, rabbit chondrocytes responded to IL-1 beta and IL-1/TNF, but not to TNF-alpha alone, with a very marked increase in extracellular sPLA2 activity.

CONCLUSION

Human articular chondrocytes synthesize and constitutively release sPLA2. Such continuous release is most probably responsible for the high concentration of sPLA2 in articular cartilage and may be the source of synovial fluid sPLA2. To our knowledge, human articular chondrocytes are the only sPLA2 producing cells tested to date that do not respond to cytokine stimulation with increased sPLA2 activity; yet enhancement was seen with 8-bromo cAMP. It seems therefore that, human articular chondrocytes possess signalling mechanisms for the release of sPLA2 unlike those from other mammalian cells. The significance of this observation remains to be elucidated.

摘要

目的

分泌型非胰腺磷脂酶A2(sPLA2)是关节炎症过程中已知的诱导剂/促进剂。它与成人及青少年类风湿关节炎的疾病活动相关。滑液中含有高浓度的sPLA2。我们发现人类关节软骨含有大量sPLA2,且培养的软骨细胞可组成性地合成并释放sPLA2。为了测试控制sPLA2释放的机制,我们将培养的人类关节软骨细胞暴露于细胞因子及其他已知可在其他细胞中诱导sPLA2的试剂中。

方法

将取自类风湿性关节炎和骨关节炎关节外观正常的软骨以及正常新生儿关节软骨的软骨细胞与兔关节软骨细胞进行比较。采用放射性标记的大肠杆菌衍生磷脂测定法以及使用抗重组人滑膜型sPLA2单克隆抗体的ELISA技术。细胞以单层形式生长,也在藻酸盐珠中生长。

结果

来自关节炎关节和新生儿关节的人类关节软骨细胞可组成性地释放sPLA2,但用白细胞介素-1β(IL-1β)、肿瘤坏死因子-α(TNF-α)、IL-6、制瘤素M、脂多糖(LPS)或福斯可林进一步刺激时无反应。当细胞暴露于8-溴环磷酸腺苷(cAMP)时,观察到明显的刺激作用。细胞以单层形式生长或在藻酸盐珠中生长并不改变结果。与人类细胞不同,兔软骨细胞对IL-1β和IL-1/TNF有反应,但单独对TNF-α无反应,细胞外sPLA2活性显著增加。

结论

人类关节软骨细胞合成并组成性地释放sPLA2。这种持续释放很可能是关节软骨中sPLA2高浓度的原因,可能是滑液中sPLA2的来源。据我们所知,人类关节软骨细胞是迄今为止测试的唯一一种sPLA2产生细胞,其sPLA2活性不会因细胞因子刺激而增加;然而用8-溴cAMP可增强其活性。因此,人类关节软骨细胞似乎拥有与其他哺乳动物细胞不同的sPLA2释放信号机制。这一观察结果的意义仍有待阐明。

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