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Cdon通过调节背侧先驱细胞聚集和库普弗小泡形态发生,对器官左右模式形成至关重要。

Cdon is essential for organ left-right patterning by regulating dorsal forerunner cells clustering and Kupffer's vesicle morphogenesis.

作者信息

Deng Zhilin, Ran Qin, Chang Wenqi, Li Chengni, Li Botong, Huang Shuying, Huang Jingtong, Zhang Ke, Li Yuanyuan, Liu Xingdong, Liang Yundan, Guo Zhenhua, 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 Ultrasound, Luzhou People's Hospital, Luzhou, China.

出版信息

Front Cell Dev Biol. 2024 Aug 22;12:1429782. doi: 10.3389/fcell.2024.1429782. eCollection 2024.

DOI:10.3389/fcell.2024.1429782
PMID:39239564
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11374761/
Abstract

and are members of the cell adhesion molecule subfamily III Ig/fibronectin. Although they have been reported to be involved in muscle and neural development at late developmental stage, their early roles in embryonic development remain unknown. Here, we discovered that in zebrafish, , but not , is expressed in dorsal forerunner cells (DFCs) and the epithelium of Kupffer's vesicle (KV), suggesting a potential role for in organ left-right (LR) patterning. Further data showed that liver and heart LR patterning were disrupted in morphants and mutants. Mechanistically, we found that loss of function led to defect in DFCs clustering, reduced KV lumen, and defective cilia, resulting in randomized Nodal/spaw signaling and subsequent organ LR patterning defects. Additionally, predominant distribution of a morpholino (MO) in DFCs caused defects in DFC clustering, KV morphogenesis, cilia number/length, Nodal/spaw signaling, and organ LR asymmetry, similar to those observed in morphants and embryos, indicating a cell-autonomous role for in regulating KV formation during LR patterning. In conclusion, our data demonstrate that during gastrulation and early somitogenesis, is essential for proper DFC clustering, KV formation, and normal cilia, thereby playing a critical role in establishing organ LR asymmetry.

摘要

[具体分子名称1]和[具体分子名称2]是细胞粘附分子亚家族III Ig/纤连蛋白的成员。尽管据报道它们在发育后期参与肌肉和神经发育,但其在胚胎发育早期的作用仍不清楚。在这里,我们发现,在斑马鱼中,[具体分子名称1]而非[具体分子名称2]在背侧先驱细胞(DFC)和库普弗囊泡(KV)的上皮中表达,这表明[具体分子名称1]在器官左右(LR)模式形成中具有潜在作用。进一步的数据表明,在[具体分子名称1]的吗啉代寡核苷酸(MO)注射胚胎和[具体分子名称1]突变体中,肝脏和心脏的LR模式形成受到破坏。从机制上讲,我们发现[具体分子名称1]功能丧失导致DFC聚集缺陷、KV腔减小和纤毛缺陷,从而导致Nodal/spaw信号随机化以及随后的器官LR模式形成缺陷。此外,DFC中[具体分子名称1]的MO的主要分布导致DFC聚集、KV形态发生、纤毛数量/长度、Nodal/spaw信号以及器官LR不对称性出现缺陷,类似于在[具体分子名称1]的MO注射胚胎和[具体分子名称1]突变体胚胎中观察到的情况,这表明[具体分子名称1]在LR模式形成过程中调节KV形成方面具有细胞自主作用。总之,我们的数据表明,在原肠胚形成和早期体节发生过程中,[具体分子名称1]对于正确的DFC聚集、KV形成和正常纤毛至关重要,从而在建立器官LR不对称性中发挥关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d9/11374761/76ec583275be/fcell-12-1429782-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d9/11374761/276b8521eee0/fcell-12-1429782-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d9/11374761/face58fc6592/fcell-12-1429782-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d9/11374761/7142741b2e82/fcell-12-1429782-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d9/11374761/6053da1bb55f/fcell-12-1429782-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d9/11374761/830e612de296/fcell-12-1429782-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d9/11374761/76ec583275be/fcell-12-1429782-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d9/11374761/276b8521eee0/fcell-12-1429782-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d9/11374761/face58fc6592/fcell-12-1429782-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d9/11374761/7142741b2e82/fcell-12-1429782-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d9/11374761/6053da1bb55f/fcell-12-1429782-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d9/11374761/830e612de296/fcell-12-1429782-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3d9/11374761/76ec583275be/fcell-12-1429782-g006.jpg

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本文引用的文献

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Front Mol Biosci. 2023 Dec 12;10:1292076. doi: 10.3389/fmolb.2023.1292076. eCollection 2023.
2
Cdon ablation in motor neurons causes age-related motor neuron degeneration and impaired sciatic nerve repair.运动神经元中的Cdon基因消融会导致与年龄相关的运动神经元退化以及坐骨神经修复受损。
J Cachexia Sarcopenia Muscle. 2023 Oct;14(5):2239-2252. doi: 10.1002/jcsm.13308. Epub 2023 Aug 9.
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Mutations in cdon and boc affect trunk neural crest cell migration and slow-twitch muscle development in zebrafish.
cdon 和 boc 基因突变会影响斑马鱼躯干神经嵴细胞的迁移和慢肌的发育。
Development. 2023 Jul 15;150(14). doi: 10.1242/dev.201304. Epub 2023 Jul 13.
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Understanding laterality disorders and the left-right organizer: Insights from zebrafish.了解左右侧发育障碍与左右组织者:来自斑马鱼的见解
Front Cell Dev Biol. 2022 Dec 23;10:1035513. doi: 10.3389/fcell.2022.1035513. eCollection 2022.
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Left-right asymmetric expression of the module in developing turtle forebrain.该模块在发育中的龟前脑的左右不对称表达。
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