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ERK信号通路调节人间充质干细胞在I型胶原和玻连蛋白上的成骨分化。

ERK signaling pathways regulate the osteogenic differentiation of human mesenchymal stem cells on collagen I and vitronectin.

作者信息

Salasznyk Roman M, Klees Robert F, Hughlock Mariah K, Plopper George E

机构信息

Department of Biology, Rensselaer Polytechnic Institute, Troy, New York 12180-3596, USA.

出版信息

Cell Commun Adhes. 2004 Sep-Dec;11(5-6):137-53. doi: 10.1080/15419060500242836.

Abstract

Adhesion to the extracellular matrix (ECM) proteins collagen I and vitronectin is sufficient to drive human mesenchymal stem cells (hMSCs) into an osteogenic differentiation pathway, but the mechanisms underlying this stimulation are not well understood. We found that addition of beta1 and alpha(v)beta3 integrin blocking antibodies inhibited ECM-induced ERK activation, while addition of the MEK inhibitor PD98059 blocked ERK activation, serine phosphorylation of the osteogenic transcription factor runx2/cbfa-1, osteogenic gene expression, and calcium deposition. These results suggest that ERK plays an important role in driving the ECM-induced osteogenic differentiation of hMSC.

摘要

与细胞外基质(ECM)蛋白I型胶原和玻连蛋白的黏附足以驱动人间充质干细胞(hMSC)进入成骨分化途径,但这种刺激的潜在机制尚不清楚。我们发现,添加β1和α(v)β3整合素阻断抗体可抑制ECM诱导的ERK激活,而添加MEK抑制剂PD98059可阻断ERK激活、成骨转录因子runx2/cbfa-1的丝氨酸磷酸化、成骨基因表达和钙沉积。这些结果表明,ERK在驱动ECM诱导的hMSC成骨分化中起重要作用。

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