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轻度冷应激会特异性地干扰斑马鱼中深层纤维细胞(DFCs)的聚集运动以及器官左右不对称模式的形成。

Mild cold stress specifically disturbs clustering movement of DFCs and sequential organ left-right patterning in zebrafish.

作者信息

Liu Min, Zou Xinyu, Fu Mao, Bai Xinping, Zhao Yongyan, Chen Xin, Wang Xiaoyu, Wang Peijian, Huang Sizhou

机构信息

Development and Regeneration Key Laboratory of Sichuan Province, Department of Anatomy and Histology and Embryology, School of Basic Medical Sciences, Chengdu Medical College, Chengdu, China.

Department of Cardiology, the First Affiliated Hospital, Chengdu Medical College, Chengdu, China.

出版信息

Front Cell Dev Biol. 2022 Sep 23;10:952844. doi: 10.3389/fcell.2022.952844. eCollection 2022.

Abstract

In poikilothermic animals, the distinct acclimatization ability of different organs has been previously addressed, while the tissue-specific role of cold stress in early development is largely unknown. In this study, we discovered that despite its role in delaying embryonic development, mild cold stress (22°C) does not disturb multiple-organ progenitor specification, but does give rise to organ left-right (LR) patterning defects. Regarding the mechanism, the data showed that mild cold stress downregulated the expression of cell-adhesion genes and during gastrulation, especially in dorsal forerunner cells (DFCs), which partially disturbed the clustering movement of DFCs, Kupffer's vesicle (KV) morphogenesis, and ciliogenesis. As a result, the defects of KV/cilia disrupted asymmetric signaling and subsequent heart and liver LR patterning. In conclusion, our data novelly identified that, in early development, DFCs are more sensitive to mild cold stress, and mild cold stress repressed the expression of cell adhesion-related gene and . This role partially disturbed the clustering movement of DFCs, which resulted in defective KV/cilia development and sequential organ LR patterning defects.

摘要

在变温动物中,不同器官独特的适应能力此前已有研究报道,而冷应激在早期发育过程中的组织特异性作用在很大程度上仍不清楚。在本研究中,我们发现,尽管轻度冷应激(22°C)会延迟胚胎发育,但其并不会干扰多器官祖细胞的特化,却会导致器官左右(LR)模式形成缺陷。关于其机制,数据显示,轻度冷应激会下调原肠胚形成期细胞黏附基因 和 的表达,尤其是在背侧前驱细胞(DFC)中,这会部分干扰DFC的聚集运动、库普弗囊泡(KV)形态发生和纤毛形成。结果,KV/纤毛的缺陷破坏了不对称信号传导以及随后心脏和肝脏的LR模式形成。总之,我们的数据首次表明,在早期发育中,DFC对轻度冷应激更为敏感,且轻度冷应激会抑制细胞黏附相关基因 和 的表达。这一作用部分干扰了DFC的聚集运动,导致KV/纤毛发育缺陷以及随后的器官LR模式形成缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8c6/9539758/09b24268ba14/fcell-10-952844-g001.jpg

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