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小鼠腭形成过程中同源框家族Hoxc的定位

Homeobox family Hoxc localization during murine palate formation.

作者信息

Hirata Azumi, Katayama Kentaro, Tsuji Takehito, Imura Hideto, Natsume Nagato, Sugahara Toshio, Kunieda Tetsuo, Nakamura Hiroaki, Otsuki Yoshinori

机构信息

Department of Anatomy and Cell Biology, Faculty of Medicine, Osaka Medical College, Takatsuki, Osaka, Japan.

Division of Functional Morphology, Department of Basic Veterinary Medicine, School of Veterinary Medicine, Nippon Veterinary and Life Science University, Musashino, Tokyo, Japan.

出版信息

Congenit Anom (Kyoto). 2016 Jul;56(4):172-9. doi: 10.1111/cga.12153.

Abstract

Homeobox genes play important roles in craniofacial morphogenesis. However, the characteristics of the transcription factor Hoxc during palate formation remain unclear. We examined the immunolocalization patterns of Hoxc5, Hoxc4, and Hoxc6 in palatogenesis of cleft palate (Eh/Eh) mice. On the other hand, mutations in the FGF/FGFR pathway are exclusively associated with syndromic forms of cleft palate. We also examined the immunolocalization of Fgfr1 and Erk1/2 to clarify their relationships with Hoxc in palatogenesis. Some palatal epithelial cells showed Hoxc5 labeling, while almost no labeling of mesenchymal cells was observed in +/+ mice. As palate formation progressed in +/+ mice, Hoxc5, Hoxc4, and Hoxc6 were observed in medial epithelial seam cells. Hoxc5 and Hoxc6 were detected in the oral epithelium. The palatal mesenchyme also showed intense staining for Fgfr1 and Erk1/2 with progression of palate formation. In contrast, the palatal shelves of Eh/Eh mice exhibited impaired horizontal growth and failed to fuse, resulting in a cleft. Hoxc5 was observed in a few epithelial cells and diffusely in the mesenchyme of Eh/Eh palatal shelves. No or little labeling of Fgfr1 and Erk1/2 was detected in the cleft palate of Eh/Eh mice. These findings suggest that Hoxc genes are involved in palatogenesis. Furthermore, there may be the differences in the localization pattern between Hoxc5, Hoxc4, and Hoxc6. Additionally, Hoxc distribution in palatal cells during palate development may be correlated with FGF signaling. (228/250 words) © 2016 Japanese Teratology Society.

摘要

同源框基因在颅面形态发生过程中发挥着重要作用。然而,转录因子Hoxc在腭形成过程中的特征仍不清楚。我们研究了腭裂(Eh/Eh)小鼠腭发生过程中Hoxc5、Hoxc4和Hoxc6的免疫定位模式。另一方面,FGF/FGFR信号通路中的突变仅与综合征型腭裂有关。我们还检测了Fgfr1和Erk1/2的免疫定位,以阐明它们在腭发生过程中与Hoxc的关系。在+/+小鼠中,一些腭上皮细胞显示Hoxc5标记,而间充质细胞几乎未观察到标记。随着+/+小鼠腭形成的进展,在内侧上皮缝细胞中观察到Hoxc5、Hoxc4和Hoxc6。在口腔上皮中检测到Hoxc5和Hoxc6。随着腭形成的进展,腭间充质对Fgfr1和Erk1/2也显示出强烈染色。相比之下,Eh/Eh小鼠的腭突水平生长受损且未能融合,导致腭裂。在Eh/Eh小鼠腭突的一些上皮细胞中观察到Hoxc5,并在间充质中呈弥漫性分布。在Eh/Eh小鼠的腭裂中未检测到或仅检测到少量Fgfr1和Erk1/2标记。这些发现表明Hoxc基因参与腭发生。此外,Hoxc5、Hoxc4和Hoxc6之间的定位模式可能存在差异。此外,腭发育过程中腭细胞中Hoxc的分布可能与FGF信号传导相关。(228/250字)©2016日本致畸学会

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