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IQGAP-2:人类结肠焦磷酸硫胺素转运体的新型相互作用伙伴。

IQGAP-2: a novel interacting partner with the human colonic thiamin pyrophosphate transporter.

机构信息

Department of Physiology/Biophysics, School of Medicine, University of California, Irvine, California, United States.

Department of Medical Research, Tibor Rubin VA Medical Center, Long Beach, California, United States.

出版信息

Am J Physiol Cell Physiol. 2024 Dec 1;327(6):C1451-C1461. doi: 10.1152/ajpcell.00484.2024. Epub 2024 Oct 14.

Abstract

The human colonic thiamin pyrophosphate transporter (hcTPPT) mediates the uptake of the microbiota-generated and phosphorylated form of vitamin B (i.e., thiamin pyrophosphate) in the large intestine. Expression of hcTPPT along the absorptive tract is restricted to the large intestine, and the transporter is exclusively localized at the apical membrane domain of the polarized epithelial cells/colonocytes. Previous studies have characterized different physiological/pathophysiological aspects of the hcTPPT system, but nothing is currently known on whether the transporter has interacting partner(s) that affect its physiology/biology. We addressed this issue using a Y2H to screen a human colonic cDNA library and have identified three putative interactors, namely IQGAP-2, SNX-6, and DMXL-1. Focusing on IQGAP-2 (whose expression in human colonocytes is the highest), we found (using fluorescent microscopy imaging and coimmunoprecipitation approaches) the putative interactor to colocalize with hcTPPT and to directly interact with the transporter. Also, overexpressing IQGAP-2 in NCM460 cells and in human primary differentiated colonoid monolayers was found to lead to significant ( < 0.01) induction in TPP uptake, while knocking down (using gene-specific siRNAs) caused significant ( < 0.01 and < 0.05) decrease in uptake. Furthermore, overexpressing IQGAP-2 in NCM460 cells was found to lead to a significant enhancement in hcTPPT protein stability. Finally, we found the expression of IQGAP-2 to be markedly suppressed in conditions/factors that negatively impact colonic TPP uptake. These results identify the IQGAP-2 as an interacting partner with the hcTPPT in human colonocytes and show that this interaction has physiological and biological consequences. This study reports on the identification of IQGAP-2 as an interacting partner with the hcTPPT in human colonocytes and how that impacts the transporter's physiology and cell biology.

摘要

人结肠硫胺素焦磷酸转运蛋白 (hcTPPT) 介导了微生物群生成和磷酸化形式的维生素 B(即硫胺素焦磷酸)在大肠中的摄取。hcTPPT 在吸收道中的表达仅限于大肠,并且该转运蛋白仅定位于极化上皮细胞/结肠细胞的顶膜域。以前的研究已经描述了 hcTPPT 系统的不同生理/病理生理方面,但目前尚不清楚该转运蛋白是否具有影响其生理学/生物学的相互作用伙伴。我们使用 Y2H 筛选了人结肠 cDNA 文库,以解决这个问题,并鉴定出三个假定的相互作用蛋白,即 IQGAP-2、SNX-6 和 DMXL-1。我们专注于 IQGAP-2(其在人结肠细胞中的表达最高),发现(使用荧光显微镜成像和共免疫沉淀方法)该假定的相互作用蛋白与 hcTPPT 共定位,并与转运蛋白直接相互作用。此外,在 NCM460 细胞和人原代分化结肠类器官单层中过表达 IQGAP-2 被发现导致 TPP 摄取显著增加(<0.01),而敲低(使用基因特异性 siRNA)导致摄取显著减少(<0.01 和 <0.05)。此外,在 NCM460 细胞中过表达 IQGAP-2 被发现导致 hcTPPT 蛋白稳定性显著增强。最后,我们发现 IQGAP-2 的表达在对结肠 TPP 摄取有负面影响的条件/因素下显著受到抑制。这些结果确定了 IQGAP-2 是人结肠细胞中 hcTPPT 的相互作用伙伴,并表明这种相互作用具有生理和生物学意义。本研究报告了 IQGAP-2 作为人结肠细胞中 hcTPPT 的相互作用伙伴的鉴定,以及这种相互作用如何影响转运蛋白的生理学和细胞生物学。

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