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Induction of heat shock protein 70 (Hsp70) by proteasome inhibitor MG 132 protects articular chondrocytes from cellular death in vitro and in vivo

机译:蛋白酶体抑制剂MG 132诱导热休克蛋白70(Hsp70)保护关节软骨细胞免受体内和体外细胞死亡

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The aim of this work was to determine whether Hsp70 overexpression via proteasome inhibitor MG132 was able to protect chondrocytes towards mono-iodoacetate (MIA) cytotoxicity both in vitro and in vivo. In vitro, overexpression of Hsp70 via MG132 was significantly able to protect chondrocytes from MIA toxicity (MTT/LDH analyses). Hsp70 essentially mediated this chondroprotective effect as demonstrated by antisense strategy. In vivo, chondrocytic overexpression of Hsp70, after a preventive intra-articular injection of MG132 in rat knee, was sufficient to decrease the severity of OA-induced MIA lesions, as demonstrated histologically and biochemically. In conclusion, intracellular overexpression of Hsp70, through proteasome inhibition, could be an interesting tool in protecting chondrocytes from cellular injuries, either necrotic or apoptotic in nature, and thus might be a novel chondroprotective modality in rat experimental OA.
机译:这项工作的目的是确定通过蛋白酶体抑制剂MG132的Hsp70过表达是否能够在体外和体内保护软骨细胞免受单碘乙酸(MIA)细胞毒性。在体外,通过MG132过度表达Hsp70能够保护软骨细胞免受MIA毒性(MTT / LDH分析)。 Hsp70本质上介导了这种软骨保护作用,如反义策略所示。在体内,预防性关节内注射MG132在大鼠膝关节中,软骨细胞Hsp70的过度表达足以降低OA诱导的MIA病变的严重程度,如组织学和生化学证明的那样。总之,通过蛋白酶体抑制,Hsp70的细胞内过表达可能是保护软骨细胞免受细胞损伤的有趣工具,无论是坏死的还是凋亡的,因此在大鼠实验性OA中可能是一种新型的软骨保护方式。

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