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RhoGTP酶刺激与氯化锶处理相关,以对抗模拟微重力诱导的多能细胞定向分化变化。

RhoGTPase stimulation is associated with strontium chloride treatment to counter simulated microgravity-induced changes in multipotent cell commitment.

作者信息

Louis Fiona, Bouleftour Wafa, Rattner Aline, Linossier Marie-Thérèse, Vico Laurence, Guignandon Alain

机构信息

INSERM, U1059, SAINBIOSE, Saint-Etienne, F-42023 France.

Université de Lyon, Saint-Etienne, F-42023 France.

出版信息

NPJ Microgravity. 2017 Jan 25;3:7. doi: 10.1038/s41526-016-0004-6. eCollection 2017.

Abstract

Microgravity-related cytoskeletal disorganization is associated with an altered balance between osteoblastogenesis and adipogenesis of multipotent cells. Strontium chloride is known to increase osteoblastogenesis and repress adipogenesis, but its effects in microgravity-related conditions have not been established. Our goal was to investigate early events in this process, focusing on RhoGTPases as controllers of cytoskeletal organization leading to stem cell commitment. We cultivated C3H10T1/2 on microspheres using a rotating wall vessel bioreactor (NASA) in order to simulate microgravity-related conditions in adipogenesis and osteoblastogenesis conditions independently. We observed that rotating wall vessel cultures presented increased adipogenesis, while osteoblastogenesis was reduced. Strontium-treated multipotent cells presented a significant repression in adipogenesis (-90 %,  < 0.001 PPARyD8) and an activation of osteoblastogenesis (+95 %,  < 0.001 bone sialoprotein and osteopontin D8), even in gravity altered conditions. We established that concomitant RhoA/Rac1 activations were associated with osteoblastogenesis enhancement and adipogenesis limitation in uncommitted cells. As vascular endothelial growth factor splicing is mechanosensitive and its signaling is central to stem cell commitment, we investigated vascular endothelial growth factor production, isoforms and receptors expressions in our conditions. We observed that vascular endothelial growth factor and receptors expressions were not significantly affected, but we found that presence of soluble vascular endothelial growth factor was associated with RhoA/Rac1 activations, whereas sequestration of vascular endothelial growth factor by cells was associated with RhoA/Rac1 inhibitions. We propose that strontium triggers secretion of vascular endothelial growth factor and the subsequent Rac1 and RhoA activations leading to repression of adipogenesis and osteogenesis stimulation validating strontium as a counter measure for microgravity-induced alteration of cell commitment.

摘要

与微重力相关的细胞骨架紊乱与多能细胞成骨分化和脂肪生成之间平衡的改变有关。已知氯化锶可增加成骨分化并抑制脂肪生成,但其在微重力相关条件下的作用尚未明确。我们的目标是研究这一过程中的早期事件,重点关注作为细胞骨架组织控制器并导致干细胞定向分化的RhoGTPases。我们使用旋转壁式生物反应器(美国国家航空航天局)在微球上培养C3H10T1/2细胞,以便分别在脂肪生成和成骨分化条件下模拟与微重力相关的条件。我们观察到旋转壁式生物反应器培养物中脂肪生成增加,而成骨分化减少。即使在重力改变的条件下,经锶处理的多能细胞的脂肪生成也受到显著抑制(-90%,P<0.001,PPARy D8),而成骨分化则被激活(+95%,P<0.001,骨唾液蛋白和骨桥蛋白D8)。我们确定,在未定向分化的细胞中,RhoA/Rac1的同时激活与成骨分化增强和脂肪生成受限有关。由于血管内皮生长因子的剪接受机械敏感性影响,其信号传导对干细胞定向分化至关重要,因此我们研究了在我们的条件下血管内皮生长因子的产生、异构体和受体表达。我们观察到血管内皮生长因子及其受体的表达没有受到显著影响,但我们发现可溶性血管内皮生长因子的存在与RhoA/Rac1的激活有关,而细胞对血管内皮生长因子的隔离与RhoA/Rac1的抑制有关。我们提出,锶触发血管内皮生长因子的分泌以及随后的Rac1和RhoA激活,导致脂肪生成受到抑制和成骨刺激,从而验证了锶作为对抗微重力诱导的细胞定向分化改变的一种措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d27/5460183/5c26553e1cce/41526_2016_4_Fig1_HTML.jpg

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