Sonic hedgehog signaling regulates a novel epithelial progenitor domain of the hindbrain choroid plexus

被引:71
作者
Huang, Xi [1 ]
Ketova, Tatiana [1 ]
Fleming, Jonathan T. [1 ]
Wang, Haibin [2 ]
Dey, Sudhansu K. [3 ]
Ying Litingtung [1 ]
Chiang, Chin [1 ]
机构
[1] Vanderbilt Univ, Med Ctr, Dept Cell & Dev Biol, Nashville, TN 37232 USA
[2] Chinese Acad Sci, Inst Zool, State Key Lab Reprod Biol, Beijing 10010, Peoples R China
[3] Cincinnati Childrens Res Fdn, Div Reprod Sci, Cincinnati, OH 45229 USA
来源
DEVELOPMENT | 2009年 / 136卷 / 15期
基金
美国国家卫生研究院;
关键词
Shh; Cerebrospinal fluid; Choroid plexus; Epithelium; Gli1; MOUSE PATCHED GENE; ROOF PLATE; CEREBROSPINAL-FLUID; NEURAL CREST; PROLIFERATION; CEREBELLUM; MIDLINE; GROWTH; CELLS; SPECIFICATION;
D O I
10.1242/dev.033795
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Choroid plexuses (ChPs) are vascularized secretory organs involved in the regulation of brain homeostasis, and function as the blood-cerebrospinal fluid (CSF) barrier. Despite their crucial roles, there is limited understanding of the regulatory mechanism driving ChP development. Sonic hedgehog (Shh), a secreted signal crucial for embryonic development and cancer, is strongly expressed in the differentiated hindbrain ChP epithelium (hChPe). However, we identify a distinct epithelial domain in the hChP that does not express Shh, but displays Shh signaling. We find that this distinct Shh target field that adjoins a germinal zone, the lower rhombic lip (LRL), functions as a progenitor domain by contributing directly to the hChPe. By conditional Shh mutant analysis, we show that Shh signaling regulates hChPe progenitor proliferation and hChPe expansion through late embryonic development, starting around E12.5. Whereas previous studies show that direct contribution to the hChPe by the LRL ceases around E14, our findings reveal a novel tissue-autonomous role for Shh production and signaling in driving the continual growth and expansion of the hindbrain choroid plexus throughout development.
引用
收藏
页码:2535 / 2543
页数:9
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