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含EH结构域蛋白2缺陷限制了腹股沟原代脂肪细胞中脂肪组织的扩张并损害了脂肪分解。

EH Domain-Containing 2 Deficiency Restricts Adipose Tissue Expansion and Impairs Lipolysis in Primary Inguinal Adipocytes.

作者信息

Fryklund Claes, Morén Björn, Shah Shrenika, Grossi Mario, Degerman Eva, Matthaeus Claudia, Stenkula Karin G

机构信息

Department of Experimental Medical Science, Lund University, Lund, Sweden.

School of Biomedical, Nutritional and Sport Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.

出版信息

Front Physiol. 2021 Sep 24;12:740666. doi: 10.3389/fphys.2021.740666. eCollection 2021.

DOI:10.3389/fphys.2021.740666
PMID:34630160
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8497890/
Abstract

Lipid uptake can be facilitated caveolae, specific plasma membrane invaginations abundantly expressed in adipocytes. The dynamin-related protein EH domain-containing 2 (EHD2) stabilizes caveolae at the cell surface. Here, we have examined the importance of EHD2 for lipid handling using primary adipocytes isolated from EHD2 knockout ( ) C57BL6/N mice. Following high-fat diet (HFD) feeding, we found a clear impairment of epididymal, but not inguinal, adipose tissue expansion in compared with (WT) mice. Cell size distribution analysis revealed that mice had a lower proportion of small adipocytes, and an accumulation of medium-sized adipocytes in both epididymal and inguinal adipose tissue. Further, PPARγ activity, FABP4 and caveolin-1 expression were decreased in adipocytes isolated from mice. Inguinal adipocytes isolated from mice displayed reduced lipolysis in response to beta adrenergic receptor agonist, which was associated with reduced phosphorylation of perilipin-1 and hormone sensitive lipase (HSL). This impairment could not be rescued using a cAMP analog, indicating that impaired lipolysis in primary adipocytes likely occurs at the level of, or downstream of, protein kinase A (PKA). Altogether, these findings pinpoint the importance of EHD2 for maintained intracellular lipid metabolism, and emphasize differences in mechanisms regulating lipid handling in various adipose-tissue depots.

摘要

脂筏可促进脂质摄取,脂筏是脂肪细胞中大量表达的特定质膜内陷结构。动力蛋白相关蛋白含EH结构域2(EHD2)可稳定细胞表面的脂筏。在此,我们使用从EHD2基因敲除( )的C57BL6/N小鼠分离的原代脂肪细胞,研究了EHD2对脂质处理的重要性。高脂饮食(HFD)喂养后,我们发现与野生型(WT)小鼠相比, 小鼠附睾脂肪组织扩张明显受损,但腹股沟脂肪组织未受损。细胞大小分布分析显示, 小鼠小脂肪细胞比例较低,附睾和腹股沟脂肪组织中中等大小脂肪细胞积累。此外,从 小鼠分离的脂肪细胞中PPARγ活性、FABP4和小窝蛋白-1表达降低。从 小鼠分离的腹股沟脂肪细胞对β肾上腺素能受体激动剂的脂解反应降低,这与 perilipin-1和激素敏感性脂肪酶(HSL)磷酸化降低有关。使用cAMP类似物无法挽救这种损伤,表明 原代脂肪细胞中脂解受损可能发生在蛋白激酶A(PKA)水平或其下游。总之,这些发现指出了EHD2对维持细胞内脂质代谢的重要性,并强调了不同脂肪组织库中调节脂质处理机制的差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f570/8497890/fac943392f72/fphys-12-740666-g006.jpg
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