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