Bmp5 Regulates Neural Crest Cell Survival and Proliferation via Two Different Signaling Pathways

被引:24
|
作者
Shih, Hung-Yu [1 ]
Hsu, Shu-Yuan [1 ,2 ]
Ouyang, Pin [1 ,2 ,3 ]
Lin, Sheng-Jia [1 ]
Chou, Ting-Yun [4 ]
Chiang, Ming-Chang [5 ]
Cheng, Yi-Chuan [1 ,6 ]
机构
[1] Chang Gung Univ, Coll Med, Grad Inst Biomed Sci, 259 Wenhua 1st Road, Taoyuan 33302, Taiwan
[2] Chang Gung Univ, Coll Med, Dept Anat, Taoyuan, Taiwan
[3] Chang Gung Univ, Mol Med Res Ctr, Taoyuan, Taiwan
[4] Chang Gung Univ, Coll Med, Dept Biomed Sci, Taoyuan, Taiwan
[5] Fu Jen Catholic Univ, Dept Life Sci, New Taipei, Taiwan
[6] Chang Gung Mem Hosp, Linkou Med Ctr, Neurosci Res Ctr, Taoyuan, Taiwan
关键词
Bmp5; Neural crest progenitors; Proliferation; Apoptosis; BONE MORPHOGENETIC PROTEINS; TGF-BETA; MORPHOLINO PHENOCOPIES; KINASE KINASE; MAP KINASE; ZEBRAFISH; FGF; SPECIFICATION; MUTATIONS; INDUCTION;
D O I
10.1002/stem.2533
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Neural crest progenitor cells, which give rise to many ectodermal and mesodermal derivatives, must maintain a delicate balance of apoptosis and proliferation for their final tissue contributions. Here we show that zebrafish bmp5 is expressed in neural crest progenitor cells and that it activates the Smad and Erk signaling pathways to regulate cell survival and proliferation, respectively. Loss-of-function analysis showed that Bmp5 was required for cell survival and this response is mediated by the Smad-Msxb signaling cascade. However, the Bmp5-Smad-Msxb signaling pathway had no effect on cell proliferation. In contrast, Bmp5 was sufficient to induce cell proliferation through the Mek-Erk-Id3 signaling cascade, whereas disruption of this signaling cascade had no effect on cell survival. Taken together, our results demonstrate an important regulatory mechanism for bone morphogenic protein-initiated signal transduction underlying the formation of neural crest progenitors.
引用
收藏
页码:1003 / 1014
页数:12
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