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星形胶质细胞中的胰岛素和胰岛素样生长因子-I 受体对行为和阿尔茨海默病样病理有不同的影响。

Insulin and insulin-like growth factor-I receptors in astrocytes exert different effects on behavior and Alzheimer´s-like pathology.

机构信息

Achucarro Basque Center for Neuroscience, Leioa, Bizkaia, 48940, Spain.

Cajal Institute, Madrid, 28002, Spain.

出版信息

F1000Res. 2022 Jun 16;11:663. doi: 10.12688/f1000research.121901.3. eCollection 2022.

DOI:10.12688/f1000research.121901.3
PMID:36636477
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9823242/
Abstract

Pleiotropic actions of insulin and insulin-like growth factor I (IGF-I) in the brain are context- and cell-dependent, but whether this holds for their receptors (insulin receptor (IR) and IGF-I receptor (IGF-IR), respectively), is less clear. We compared mice lacking IR or IGF-IR in glial fibrillary astrocytic protein (GFAP)-expressing astrocytes in a tamoxifen-regulated manner, to clarify their role in this type of glial cells, as the majority of data of their actions in brain have been obtained in neurons. We observed that mice lacking IR in GFAP astrocytes (GFAP IR KO mice) develop mood disturbances and maintained intact cognition, while at the same time show greater pathology when cross-bred with APP/PS1 mice, a model of familial Alzheimer´s disease (AD). Conversely, mice lacking IGF-IR in GFAP astrocytes (GFAP-IGF-IR KO mice) show cognitive disturbances, maintained mood tone, and show control-dependent changes in AD-like pathology. These observations confirm that the role of IR and IGF-IR in the brain is cell-specific and context-dependent.

摘要

胰岛素和胰岛素样生长因子 I (IGF-I) 在大脑中的多效作用取决于环境和细胞,但它们的受体(胰岛素受体 (IR) 和 IGF-I 受体 (IGF-IR))是否也是如此则不太清楚。我们通过他莫昔芬调控的方式,比较了在神经胶质纤维酸性蛋白 (GFAP) 表达星形胶质细胞中缺乏 IR 或 IGF-IR 的小鼠,以阐明它们在这种类型的胶质细胞中的作用,因为关于它们在大脑中的作用的大多数数据都是在神经元中获得的。我们观察到,缺乏 GFAP 星形胶质细胞中 IR 的小鼠(GFAP IR KO 小鼠)表现出情绪障碍,认知功能完好,而同时与 APP/PS1 小鼠(家族性阿尔茨海默病 (AD) 的模型)杂交时则表现出更大的病理变化。相反,缺乏 GFAP 星形胶质细胞中 IGF-IR 的小鼠(GFAP-IGF-IR KO 小鼠)表现出认知障碍,情绪状态保持正常,但在 AD 样病理方面表现出与控制相关的变化。这些观察结果证实,IR 和 IGF-IR 在大脑中的作用是细胞特异性和环境依赖性的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00c4/9823269/ff756b62f7d4/f1000research-11-142193-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00c4/9823269/a89ff49a8042/f1000research-11-142193-g0000.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00c4/9823269/7fd2a3ccc42c/f1000research-11-142193-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00c4/9823269/e82ea6ecf239/f1000research-11-142193-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00c4/9823269/8fd4cf8c15d9/f1000research-11-142193-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00c4/9823269/ff756b62f7d4/f1000research-11-142193-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00c4/9823269/a89ff49a8042/f1000research-11-142193-g0000.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00c4/9823269/7fd2a3ccc42c/f1000research-11-142193-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00c4/9823269/e82ea6ecf239/f1000research-11-142193-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00c4/9823269/8fd4cf8c15d9/f1000research-11-142193-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00c4/9823269/ff756b62f7d4/f1000research-11-142193-g0004.jpg

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