Roles of GTP and Rho GTPases in pancreatic islet beta cell function and dysfunction.

Q2 Biochemistry, Genetics and Molecular Biology
Anjaneyulu Kowluru
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引用次数: 8

Abstract

A growing body of evidence implicates requisite roles for GTP and its binding proteins (Rho GTPases) in the cascade of events leading to physiological insulin secretion from the islet beta cell. Interestingly, chronic exposure of these cells to hyperglycaemic conditions appears to result in sustained activation of specific Rho GTPases (e.g. Rac1) leading to significant alterations in cellular functions including defects in mitochondrial function and nuclear collapse culminating in beta cell demise. One of the objectives of this review is to highlight our current understanding of the regulatory roles of GTP and Rho GTPases in normal islet function (e.g. proliferation and insulin secretion) as well potential defects in these signalling molecules and metabolic pathways that could contribute islet beta cell dysfunction and loss of functional beta cell mass leading to the onset of diabetes. Potential knowledge gaps in this field and possible avenues for future research are also highlighted.Abbreviations: ARNO: ADP-ribosylation factor nucleotide binding site opener; CML: carboxyl methylation; Epac: exchange protein directly activated by cAMP; ER stress: endoplasmic reticulum stress; FTase: farnesyltransferase; GAP: GTPase activating protein; GDI: GDP dissociation inhibitor; GEF: guanine nucleotide exchange factor; GGTase: geranylgeranyltransferase; GGpp: geranylgeranylpyrophosphate; GGPPS: geranylgeranyl pyrophosphate synthase; GSIS: glucose-stimulated insulin secretion; HGPRTase: hypoxanthine-guanine phosphoribosyltransferase; IMPDH: inosine monophosphate dehydrogenase; α-KIC: α-ketoisocaproic acid; MPA: mycophenolic acid; MVA: mevalonic acid; NDPK: nucleoside diphosphate kinase; NMPK: nucleoside monophosphate kinase; Nox2: phagocyte-like NADPH oxidase; PAK-I: p21-activated kinase-I; β-PIX: β-Pak-interacting exchange factor; PRMT: protein arginine methyltransferase; Rac1: ras-related C3 botulinum toxin substrate 1; Tiam1: T-cell lymphoma invasion and metastasis-inducing protein 1; Trx-1: thioredoxin-1; Vav2: vav guanine nucleotide exchange factor 2.

GTP和Rho GTP酶在胰岛细胞功能和功能障碍中的作用。
越来越多的证据表明,GTP及其结合蛋白(Rho GTP酶)在导致胰岛β细胞生理性胰岛素分泌的级联事件中起着必要的作用。有趣的是,这些细胞长期暴露于高血糖条件下似乎会导致特异性Rho gtpase(例如Rac1)的持续激活,从而导致细胞功能的显著改变,包括线粒体功能缺陷和核崩溃,最终导致β细胞死亡。本综述的目的之一是强调我们目前对GTP和Rho GTP酶在正常胰岛功能(如增殖和胰岛素分泌)中的调节作用的理解,以及这些信号分子和代谢途径中的潜在缺陷,这些缺陷可能导致胰岛β细胞功能障碍和功能性β细胞质量的丧失,从而导致糖尿病的发生。该领域的潜在知识缺口和未来研究的可能途径也得到了强调。缩写:ARNO: adp -核糖基化因子核苷酸结合位点开启剂;CML:羧基甲基化;Epac: cAMP直接激活的交换蛋白;内质网应激:内质网应激;简称ftis:治疗;GAP: GTPase激活蛋白;GDI: GDP解离抑制剂;GEF:鸟嘌呤核苷酸交换因子;GGTase: geranylgeranyltransferase;GGpp: geranylgeranylpyrophosphate;香叶基焦磷酸合成酶;GSIS:葡萄糖刺激胰岛素分泌;HGPRTase:次黄嘌呤-鸟嘌呤磷酸核糖基转移酶;磷酸肌苷脱氢酶;α-KIC: α-酮异己酸;MPA:霉酚酸;MVA:甲羟戊酸;NDPK:核苷二磷酸激酶;核苷单磷酸激酶;Nox2:吞噬细胞样NADPH氧化酶;PAK-I: p21活化激酶i;β-PIX: β- pak相互作用交换因子;PRMT:蛋白精氨酸甲基转移酶;Rac1: ras相关C3肉毒毒素底物1;Tiam1: t细胞淋巴瘤侵袭转移诱导蛋白1;Trx-1: thioredoxin-1;Vav2: vav鸟嘌呤核苷酸交换因子2。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Small GTPases
Small GTPases Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
6.10
自引率
0.00%
发文量
6
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