Source:http://linkedlifedata.com/resource/pubmed/id/20623582
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
3
|
| pubmed:dateCreated |
2010-9-2
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| pubmed:abstractText |
p130Cas, Crk-associated substrate (Cas), is an adaptor/scaffold protein that plays a central role in actin cytoskeletal reorganization. We previously showed that mice in which Cas was deleted (Cas(-/-)) died in utero because of early cardiovascular maldevelopment. To further investigate the in vivo roles of Cas, we generated mice with a hypomorphic Cas allele lacking the exon 2-derived region (Cas(Deltaex2/Deltaex2)), which encodes Src homology domain 3 (SH3) of Cas. Cas(Deltaex2/Deltaex2) mice again died as embryos, but they particularly showed progressive liver degeneration with hepatocyte apoptosis. Because Cas expression in the liver is preferentially detected in sinusoidal endothelial cells (SECs), the observed hepatocyte apoptosis was most likely ascribable to impaired function of SECs. To address this possibility, we stably introduced a Cas mutant lacking the SH3 domain (Cas DeltaSH3) into an SEC line (NP31). Intriguingly, the introduction of Cas DeltaSH3 induced a loss of fenestrae, the characteristic cell-penetrating pores in SECs that serve as a critical route for supplying oxygen and nutrients to hepatocytes. The disappearance of fenestrae in Cas DeltaSH3-expressing cells was associated with an attenuation of actin stress fiber formation, a marked reduction in tyrosine phosphorylation of Cas, and defective binding of Cas to CrkII. CONCLUSION: Cas plays pivotal roles in liver development through the reorganization of the actin cytoskeleton and formation of fenestrae in SECs.
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| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:citationSubset |
IM
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| pubmed:chemical | |
| pubmed:status |
MEDLINE
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| pubmed:month |
Sep
|
| pubmed:issn |
1527-3350
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| pubmed:author | |
| pubmed:issnType |
Electronic
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| pubmed:volume |
52
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| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
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| pubmed:pagination |
1089-99
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| pubmed:meshHeading |
pubmed-meshheading:20623582-Actins,
pubmed-meshheading:20623582-Animals,
pubmed-meshheading:20623582-Apoptosis,
pubmed-meshheading:20623582-Cell Line,
pubmed-meshheading:20623582-Cell Surface Extensions,
pubmed-meshheading:20623582-Crk-Associated Substrate Protein,
pubmed-meshheading:20623582-Cytoskeleton,
pubmed-meshheading:20623582-Endothelium,
pubmed-meshheading:20623582-Exons,
pubmed-meshheading:20623582-Female,
pubmed-meshheading:20623582-Hepatocytes,
pubmed-meshheading:20623582-Liver,
pubmed-meshheading:20623582-Male,
pubmed-meshheading:20623582-Mice,
pubmed-meshheading:20623582-Mice, Inbred C57BL,
pubmed-meshheading:20623582-Models, Animal,
pubmed-meshheading:20623582-Phosphorylation,
pubmed-meshheading:20623582-Rats
|
| pubmed:year |
2010
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| pubmed:articleTitle |
p130Cas, Crk-associated substrate plays essential roles in liver development by regulating sinusoidal endothelial cell fenestration.
|
| pubmed:affiliation |
Department of Disease Model, Hiroshima University, Hiroshima, Japan.
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| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|