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首页> 外文期刊>American Journal of Physiology >Endocytosis of collagen by hepatic stellate cells regulates extracellular matrix dynamics
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Endocytosis of collagen by hepatic stellate cells regulates extracellular matrix dynamics

机译:肝星状细胞胶原蛋白的内吞作用调节细胞外基质动力学

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摘要

Hepatic stellate cells (HSCs) generate matrix, which in turn may also regulate HSCs function during liver fibrosis. We hypothesized that HSCs may endocytose matrix proteins to sense and respond to changes in microenvironment. Primary human HSCs, LX2, or mouse embryonic fibroblasts (MEFs) [wild-type; c-ablw~; or Yes, Src, and Fyn knockout mice (YSF"7")] were incubated with fluorescent-labeled collagen or gelatin. Fluorescence-activated cell sorting analysis and confocal microscopy were used for measuring cellular internalization of matrix proteins. Targeted PCR array and quantitative real-time PCR were used to evaluate gene expression changes. HSCs and LX2 cells endocytose collagens in a concentration- and time-dependent manner. Endocytosed collagen colocalized with Dextran 10K, a marker of macropinocytosis, and 5-ethylisopropyl amiloride, an inhibitor of macropinocytosis, reduced collagen internalization by 46%. Cytocha-lasin D and ML7 blocked collagen internalization by 47% and 45%, respectively, indicating that actin and myosin are critical for collagen endocytosis. Wortmannin and AKT inhibitor blocked collagen internalization by 70% and 89%, respectively, indicating that matrix macropinocytosis requires phosphoinositide-3-kinase (PI3K)/AKT signaling. Overexpression of dominant-negative dynamin-2 K44A blocked matrix internalization by 77%, indicating a role for dynamin-2 in matrix macropinocytosis. Whereas c-abl""7" MEF showed impaired matrix endocytosis, YSF~7~ MEF surprisingly showed increased matrix endocytosis. It was also associated with complex gene regulations that related with matrix dynamics, including increased matrix metalloproteinase 9 (MMP-9) mRNA levels and zymographic activity. HSCs endocytose matrix proteins through macropinocytosis that requires a signaling network composed of PI3K/AKT, dynamin-2, and c-abl. Interaction with extracellular matrix regulates matrix dynamics through modulating multiple gene expressions including MMP-9.
机译:肝星状细胞(HSCs)产生基质,其又可以调节肝纤维化期间的HSC功能。我们假设HSCs可以内核蛋白质蛋白感测和响应微环境的变化。原发性人HSC,LX2或小鼠胚胎成纤维细胞(MEFS)[野生型; c-ablw〜;或者,SRC和FYN淘汰小鼠(YSF“7”)]与荧光标记的胶原或明胶一起温育。荧光激活的细胞分选分析和共聚焦显微镜用于测量基质蛋白的细胞内化。靶向PCR阵列和定量实时PCR用于评估基因表达的变化。 HSC和LX2细胞以浓度和时间依赖性方式内核细胞胶粘剂。用葡聚糖10K分致大致胶原化的内核细胞化胶原蛋白,癌细胞增生率分子和5-乙基异丙基氨基胺,癌细胞抑制剂,减少46%的胶原内化。细胞蛋白-Vasin D和ML7分别阻断胶原蛋白内化47%和45%,表明肌动蛋白和肌球蛋白对于胶原蛋白的内吞作用至关重要。 Wortmannin和Akt抑制剂分别阻断了胶原蛋白的内化分别为70%和89%,表明基质癌细胞增生症需要磷酸阳性-3-激酶(PI3K)/ AKT信号传导。显性阴性动力学-2K44A阻断基质内化的过度表达77%,表明动力学-2在基质癌细胞中的作用。而C-ABL“7”MEF显示基质内吞作用受损,YSF〜7〜MEF令人惊讶地显示出增加的基质内吞作用。它还与与基质动态相关的复杂基因规定有关,包括增加的基质金属蛋白酶9(MMP-9)mRNA水平和致释物活性。HSCs通过大血细胞瘤蛋白质通过癌细胞蛋白,其需要由PI3K / AKT,发动机-2和C-ABL组成的信号网络。与细胞外基质的相互作用通过调节包括MMP-9的多个基因表达来调节基质动态。

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