Suppr超能文献

鼠肾脂蛋白脂肪酶:营养状态和高脂肪饮食的影响。

Lipoprotein lipase in mouse kidney: effects of nutritional status and high-fat diet.

机构信息

Department of Medical Biosciences/Physiological Chemistry, Umeå University , Umeå , Sweden.

Wallenberg Center for Molecular Medicine, Umeå University , Umeå , Sweden.

出版信息

Am J Physiol Renal Physiol. 2019 Mar 1;316(3):F558-F571. doi: 10.1152/ajprenal.00474.2018. Epub 2019 Jan 30.

Abstract

Activity of lipoprotein lipase (LPL) is high in mouse kidney, but the reason is poorly understood. The aim was to characterize localization, regulation, and function of LPL in kidney of C57BL/6J mice. We found LPL mainly in proximal tubules, localized inside the tubular epithelial cells, under all conditions studied. In fed mice, some LPL colocalized with the endothelial markers CD31 and GPIHBP1 and could be removed by perfusion with heparin, indicating a vascular location. The role of angiopoietin-like protein 4 (ANGPTL4) for nutritional modulation of LPL activity was studied in wild-type and Angptl4 mice. In Angptl4 mice, kidney LPL activity remained high in fasted animals, indicating that ANGPTL4 is involved in suppression of LPL activity on fasting, like in adipose tissue. The amount of ANGPTL4 protein in kidney was low, and the protein appeared smaller in size, compared with ANGPTL4 in heart and adipose tissue. To study the influence of obesity, mice were challenged with high-fat diet for 22 wk, and LPL was studied after an overnight fast compared with fasted mice given food for 3 h. High-fat diet caused blunting of the normal adaptation of LPL activity to feeding/fasting in adipose tissue, but in kidneys this adaptation was lost only in male mice. LPL activity increases to high levels in mouse kidney after feeding, but as no difference in uptake of chylomicron triglycerides in kidneys is found between fasted and fed states, our data confirm that LPL appears to have a minor role for lipid uptake in this organ.

摘要

脂蛋白脂肪酶 (LPL) 在小鼠肾脏中的活性很高,但原因尚不清楚。本研究旨在阐明 C57BL/6J 小鼠肾脏中 LPL 的定位、调节和功能。我们发现,在所有研究条件下,LPL 主要位于近端肾小管内,定位于肾小管上皮细胞内。在进食的小鼠中,一些 LPL 与内皮标志物 CD31 和 GPIHBP1 共定位,并用肝素灌注可以将其去除,表明其位于血管位置。在野生型和 Angptl4 小鼠中研究了血管生成素样蛋白 4 (ANGPTL4) 对 LPL 活性的营养调节作用。在 Angptl4 小鼠中,禁食动物的肾脏 LPL 活性仍然很高,表明 ANGPTL4 像在脂肪组织中一样,参与了禁食时 LPL 活性的抑制。与心脏和脂肪组织中的 ANGPTL4 相比,肾脏中 ANGPTL4 蛋白的含量较低,且蛋白的大小较小。为了研究肥胖的影响,用高脂肪饮食对小鼠进行了 22 周的挑战,然后在禁食过夜后与禁食 3 小时的小鼠进行比较,研究 LPL。高脂肪饮食导致脂肪组织中 LPL 活性对进食/禁食的正常适应减弱,但在肾脏中,这种适应仅在雄性小鼠中丢失。进食后,小鼠肾脏中的 LPL 活性升高至高水平,但由于禁食和进食状态下肾脏对乳糜微粒甘油三酯的摄取没有差异,我们的数据证实 LPL 在该器官中的脂质摄取中似乎作用较小。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验