Department of Molecular Medicine, Cornell University, Ithaca, NY 14853-6401, USA.
J Physiol. 2010 Sep 15;588(Pt 18):3499-509. doi: 10.1113/jphysiol.2010.190116. Epub 2010 Jul 19.
The modulation of endocytosis following exocytosis by noradrenaline (NA), a physiological inhibitor of insulin secretion, was investigated in INS 832/13 cells using patch-clamp capacitance measurements. Endocytosis was inhibited by NA in a pertussis toxin-insensitive manner. Dialysing a synthetic peptide mimicking the C-terminus of the α-subunit of G(z) into the cells blocked the inhibition of endocytosis by NA. Cell-attached capacitance measurements indicated that inhibition by NA was due to a decreased number of endocytotic events without a change in vesicle size. Analysis of fission pore closure kinetics revealed two distinct fission modes, with NA selectively inhibiting the rapid fission pore closure events. Comparison of the actions of NA and deltamethrin, a calcineurin antagonist and potent inhibitor of endocytosis, demonstrated that they inhibit endocytosis by different mechanisms. These findings establish novel actions for NA and G(z) in insulin-secreting cells and possibly other cell types.
本文使用膜片钳电容测量法研究去甲肾上腺素(NA)对 INS 832/13 细胞胞吐作用后内吞作用的调节作用。去甲肾上腺素以百日咳毒素不敏感的方式抑制内吞作用。将模拟 G(z)α亚基 C 末端的合成肽注入细胞内,可以阻断去甲肾上腺素对内吞作用的抑制。细胞贴附电容测量表明,去甲肾上腺素的抑制作用是由于内吞事件的数量减少,而囊泡大小没有变化。裂变孔关闭动力学分析显示存在两种不同的裂变模式,去甲肾上腺素选择性抑制快速裂变孔关闭事件。去甲肾上腺素和除虫菊酯(一种钙调神经磷酸酶拮抗剂和有效的内吞作用抑制剂)作用的比较表明,它们通过不同的机制抑制内吞作用。这些发现为胰岛素分泌细胞和可能的其他细胞类型中去甲肾上腺素和 G(z)的新作用提供了依据。