Source:http://linkedlifedata.com/resource/pubmed/id/19914233
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2010-1-27
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pubmed:abstractText |
The fine-tuning of BMP signals is critical for many aspects of complex organogenesis. In this report, we show that the augmentation of BMP signaling by a BMP-binding secreted factor, Crossveinless2 (Cv2), is essential for the early embryonic development of mammalian nephrons. In the Cv2-null mouse, the number of cap condensates (clusters of nephron progenitors, which normally express Cv2) was decreased, and the condensate cells exhibited a reduced level of aggregation. In these Cv2(-/-) condensates, the level of phosphorylated Smad1 (pSmad1) was substantially lowered. The loss of a Bmp7 allele in the Cv2(-/-) mouse enhanced the cap condensate defects and further decreased the level of pSmad1 in this tissue. These observations indicated that Cv2 has a pro-BMP function in early nephrogenesis. Interestingly, the renal defects of the Cv2(-/-) mutant were totally suppressed by a null mutation of Twisted gastrulation (Tsg), which encodes another BMP-binding factor, showing that Cv2 exerts its pro-BMP nephrogenic function Tsg-dependently. By using an embryonic kidney cell line, we presented experimental evidence showing that Cv2 enhances pro-BMP activity of Tsg. These findings revealed the molecular hierarchy between extracellular modifiers that orchestrate local BMP signal peaks in the organogenetic microenvironment.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Bone Morphogenetic Protein 7,
http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/crossveinless 2 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/twisted gastrulation protein, mouse
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
1095-564X
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2009 Elsevier Inc. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
15
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pubmed:volume |
337
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
405-14
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pubmed:meshHeading |
pubmed-meshheading:19914233-Animals,
pubmed-meshheading:19914233-Bone Morphogenetic Protein 7,
pubmed-meshheading:19914233-Carrier Proteins,
pubmed-meshheading:19914233-Cell Aggregation,
pubmed-meshheading:19914233-Cells, Cultured,
pubmed-meshheading:19914233-Epistasis, Genetic,
pubmed-meshheading:19914233-Kidney Tubules, Collecting,
pubmed-meshheading:19914233-Mice,
pubmed-meshheading:19914233-Mutation,
pubmed-meshheading:19914233-Nephrons,
pubmed-meshheading:19914233-Phenotype,
pubmed-meshheading:19914233-Proteins,
pubmed-meshheading:19914233-Signal Transduction
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pubmed:year |
2010
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pubmed:articleTitle |
Cv2, functioning as a pro-BMP factor via twisted gastrulation, is required for early development of nephron precursors.
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pubmed:affiliation |
Organogenesis and Neurogenesis Group, RIKEN Center for Developmental Biology, 2-2-3 Minatojima-minamimachi, Chuo, Kobe 650-0047, Japan. mikeya@cdb.riken.jp
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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