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Endocytosis-Dominated Membrane Area Decrease Requires Rab5 Protein in Rat Melanotrophs

机译:内吞作用 - 主导的膜面积减少需要大鼠素萎缩的Rab5蛋白

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Eukaryotic cells internalize extracellular macromolecules by endocytosis and it was shown that Rab5 protein is required for this process. While it is clear that endocytosis consists of vesicle fission from the plasma membrane, the role of Rab5 protein in the plasma membrane surface area changes is still unclear. Here we studied whether Rab5 is required for membrane surface area changes in rat melanotrophs-cells deriving from the pituitary pars intermedia. The presence of this protein in melanotrophs was probed by immunocytochemistry and its putative role in membrane area dynamics was monitored electrophysiologically with membrane capacitance measurements as this parameter directly reflects changes in membrane surface area. We found that Rab5 protein exists in melanotrophs. At [Ca~(2+)]_i < 3 μM, endocytosis-dominated membrane capacitance decrease was found to be blocked by microinjection of specific Rab5 antibody. At high [Ca~(2+)]-i, Rab5 antibody did not affect the steady-state increase in membrane capacitance, while it elevated the rate of membrane capacitance increase, which is consistent with an inhibition of endocytosis.
机译:真核细胞通过内吞作用内化细胞外大分子,结果表明该方法需要RAB5蛋白。虽然很明显,内吞作用由血浆膜的囊泡裂变组成,但是RAB5蛋白在质膜表面区域变化中的作用仍不清楚。在这里,我们研究了Rab5是否需要膜表面积的膜表面积变化,从垂体分析中源性垂直的大鼠素萎缩细胞。通过免疫细胞化学探测MelanoTrophs在丝体中存在这种蛋白质的存在,并且在膜面积动态中的调用作用在电生理学上用膜电容测量进行电脑电容测量,因为该参数直接反映膜表面积的变化。我们发现褐藻剂存在Rab5蛋白。在[Ca〜(2 +)] _ i <3μm时,发现通过特异性Rab5抗体的显微注射抑制内吞作用膜电容减少。在高[Ca〜(2 +)] - I中,Rab5抗体不会影响膜电容的稳态增加,而它升高了膜电容增加的速率,这与抑制内吞作用一致。

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