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生长分化因子 15 在白细胞介素-6 合作下对移植棕色脂肪组织存活的新作用。

New Role for Growth/Differentiation Factor 15 in the Survival of Transplanted Brown Adipose Tissues in Cooperation with Interleukin-6.

机构信息

Department of Disease Control, Research Institute, National Center for Global Health and Medicine, Tokyo 162-8655, Japan.

Department of Laboratory Molecular Genetics of Hematology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo 113-8510, Japan.

出版信息

Cells. 2020 Jun 1;9(6):1365. doi: 10.3390/cells9061365.

DOI:10.3390/cells9061365
PMID:32492819
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7349565/
Abstract

To identify factors involved in the earliest phase of the differentiation of human embryonic stem cells (hESCs) into brown adipocytes (BAs), we performed multi-time point microarray analyses. We found that growth/differentiation factor 15 (GDF15) expressions were specifically upregulated within three days of differentiation, when expressions of immature hESC markers were sustained. Although GDF15 expressions continued to increase in the subsequent differentiation phases, -deficient hESCs differentiated into mature BAs (Day 10) without apparent abnormalities. In addition, -deficient mice had normal brown adipose tissue (BAT) and were metabolically healthy. Unexpectedly, we found that interleukin-6 (IL6) expression was significantly lowered in the BAT of mice. In addition, hESCs showed abortive IL6 expressions in the later phase (>Day 6) of the differentiation. Interestingly, GDF15 expression was markedly repressed throughout the whole course of the differentiation of hESCs into BAs, indicating IL6 is essential for the induction of GDF15 in the differentiation of hESCs. Finally, intraperitoneally transplanted BAT grafts of donor mice, but not those of wild-type (WT) mice, failed in the long-term survival (12 weeks) in recipient mice. Collectively, GDF15 is required for long-term survival of BAT grafts by creating a mutual gene induction loop with IL6.

摘要

为了鉴定涉及人胚胎干细胞(hESC)向棕色脂肪细胞(BA)分化的最早阶段的因素,我们进行了多次时间点的微阵列分析。我们发现,生长/分化因子 15(GDF15)的表达在分化的头三天特异性地上调,此时未成熟的 hESC 标志物的表达持续。尽管 GDF15 的表达在随后的分化阶段继续增加,但-缺陷型 hESC 分化为成熟的 BAs(第 10 天)而没有明显的异常。此外,-缺陷型小鼠具有正常的棕色脂肪组织(BAT),且代谢健康。出乎意料的是,我们发现-缺陷型小鼠的 BAT 中白细胞介素 6(IL6)的表达显著降低。此外,-缺陷型 hESC 在分化的后期(>第 6 天)显示出 IL6 表达的中止。有趣的是,GDF15 的表达在-缺陷型 hESC 向 BAs 分化的整个过程中明显受到抑制,表明 IL6 对于诱导 hESC 分化中 GDF15 的表达是必需的。最后,-供体小鼠的 BAT 移植物经腹腔移植后,在受体小鼠中不能长期存活(12 周),而 WT 小鼠的 BAT 移植物则可以。总之,GDF15 通过与 IL6 建立相互基因诱导环,对 BAT 移植物的长期存活是必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc1b/7349565/08644cf42f59/cells-09-01365-g009.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc1b/7349565/15cf19198f8f/cells-09-01365-g007a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc1b/7349565/a68b1c71aded/cells-09-01365-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc1b/7349565/08644cf42f59/cells-09-01365-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc1b/7349565/cbf7844ea22d/cells-09-01365-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc1b/7349565/e9e242a54421/cells-09-01365-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc1b/7349565/a81b9a54e229/cells-09-01365-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc1b/7349565/c932eb0f43c5/cells-09-01365-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc1b/7349565/9fa35fec11c6/cells-09-01365-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc1b/7349565/10a0c7872319/cells-09-01365-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc1b/7349565/15cf19198f8f/cells-09-01365-g007a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc1b/7349565/a68b1c71aded/cells-09-01365-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc1b/7349565/08644cf42f59/cells-09-01365-g009.jpg

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