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促胃液素释放肽受体2参与非洲爪蟾神经嵴细胞迁移和基板模式形成。

Latrophilin2 is involved in neural crest cell migration and placode patterning in Xenopus laevis.

作者信息

Yokote Natsumi, Suzuki-Kosaka Marianna Y, Michiue Tatsuo, Hara Takahiko, Tanegashima Kosuke

机构信息

Stem Cell Project, Tokyo Metropolitan Institute of Medical Science, Setagaya-ku, Tokyo, Japan.

出版信息

Int J Dev Biol. 2019;63(1-2):29-35. doi: 10.1387/ijdb.180184kt.

Abstract

Latrophilin2 (Lphn2) is an adhesion-class of G protein-coupled receptor with an unknown function in development. Here, we show that Xenopus laevis lphn2 (Xlphn2) is involved in the migration and differentiation of neural crest (NC) cells and placode patterning in Xenopus laevis embryos. Although Xlphn2 mRNA was detected throughout embryogenesis, it was expressed more abundantly in the placode region. Morpholino antisense oligonucleotide-mediated knockdown of Xlphn2 caused abnormal migration of NC cells, irregular epibranchial placode segmentation, and defective cartilage formation. Transplantation of fluorescently-labeled NC regions of wild-type embryos into Xlphn2 morpholino-injected embryos reproduced the defective NC cell migration, indicating that Xlphn2 regulates the migration of NC cells in a non-cell autonomous manner. Our results suggest that Xlphn2 is essential for placode patterning and as a guidance molecule for NC cells.

摘要

促胃液素释放肽受体2(Lphn2)是一种粘附类G蛋白偶联受体,在发育过程中的功能尚不清楚。在此,我们表明非洲爪蟾的促胃液素释放肽受体2(Xlphn2)参与非洲爪蟾胚胎中神经嵴(NC)细胞的迁移和分化以及基板模式形成。虽然在整个胚胎发育过程中都检测到了Xlphn2 mRNA,但它在基板区域表达更为丰富。吗啉代反义寡核苷酸介导的Xlphn2敲低导致NC细胞迁移异常、鳃上基板分割不规则以及软骨形成缺陷。将野生型胚胎的荧光标记NC区域移植到注射了Xlphn2吗啉代的胚胎中,重现了有缺陷的NC细胞迁移,表明Xlphn2以非细胞自主方式调节NC细胞的迁移。我们的结果表明,Xlphn2对于基板模式形成至关重要,并且是NC细胞的导向分子。

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