| pubmed-article:1551474 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:1551474 | lifeskim:mentions | umls-concept:C0027882 | lld:lifeskim |
| pubmed-article:1551474 | lifeskim:mentions | umls-concept:C0927232 | lld:lifeskim |
| pubmed-article:1551474 | lifeskim:mentions | umls-concept:C0076560 | lld:lifeskim |
| pubmed-article:1551474 | lifeskim:mentions | umls-concept:C0033414 | lld:lifeskim |
| pubmed-article:1551474 | lifeskim:mentions | umls-concept:C0205100 | lld:lifeskim |
| pubmed-article:1551474 | lifeskim:mentions | umls-concept:C1522240 | lld:lifeskim |
| pubmed-article:1551474 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:1551474 | pubmed:dateCreated | 1992-4-27 | lld:pubmed |
| pubmed-article:1551474 | pubmed:abstractText | Thrombospondin (TSP) is a prominent constituent of the extracellular matrix of the developing nervous system. We have examined the effects of TSP on the morphological differentiation of neurons. In short-term cultures (less than or equal to 24 hr) of embryonic rat sympathetic neurons, TSP stimulated neurite outgrowth, causing significant increase in the number of processes and their length. Similar effects were observed in cultures of rat dorsal root ganglion, hippocampal, and cerebral cortical neurons. Moreover, in cultures of central neurons, TSP was more effective than laminin in enhancing process extension. Analysis of long-term (5-7 days) cultures of sympathetic neurons indicated that processes formed in the presence of TSP had the cytochemical characteristics of axons. Thus, TSP can influence neuronal development by selectively enhancing axonal growth. The neurite-promoting region of the molecule was identified using a panel of monoclonal antibodies targeted to different regions of the protein. Process outgrowth could be totally inhibited with antibody A4.1, which recognizes the stalk region of TSP. These data suggest that the neurite-promoting activity is localized to a single region of the TSP molecule. | lld:pubmed |
| pubmed-article:1551474 | pubmed:language | eng | lld:pubmed |
| pubmed-article:1551474 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1551474 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:1551474 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:1551474 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:1551474 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:1551474 | pubmed:issn | 0012-1606 | lld:pubmed |
| pubmed-article:1551474 | pubmed:author | pubmed-author:FrazierW AWA | lld:pubmed |
| pubmed-article:1551474 | pubmed:author | pubmed-author:HigginsDD | lld:pubmed |
| pubmed-article:1551474 | pubmed:author | pubmed-author:OsterhoutD... | lld:pubmed |
| pubmed-article:1551474 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:1551474 | pubmed:volume | 150 | lld:pubmed |
| pubmed-article:1551474 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:1551474 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:1551474 | pubmed:pagination | 256-65 | lld:pubmed |
| pubmed-article:1551474 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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| pubmed-article:1551474 | pubmed:meshHeading | pubmed-meshheading:1551474-... | lld:pubmed |
| pubmed-article:1551474 | pubmed:year | 1992 | lld:pubmed |
| pubmed-article:1551474 | pubmed:articleTitle | Thrombospondin promotes process outgrowth in neurons from the peripheral and central nervous systems. | lld:pubmed |
| pubmed-article:1551474 | pubmed:affiliation | Department of Pharmacology and Therapeutics, School of Medicine, State University of New York, Buffalo 14214. | lld:pubmed |
| pubmed-article:1551474 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:1551474 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
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