pubmed-article:19246034 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:19246034 | lifeskim:mentions | umls-concept:C0007634 | lld:lifeskim |
pubmed-article:19246034 | lifeskim:mentions | umls-concept:C0001721 | lld:lifeskim |
pubmed-article:19246034 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
pubmed-article:19246034 | lifeskim:mentions | umls-concept:C1537665 | lld:lifeskim |
pubmed-article:19246034 | lifeskim:mentions | umls-concept:C1879547 | lld:lifeskim |
pubmed-article:19246034 | lifeskim:mentions | umls-concept:C2911684 | lld:lifeskim |
pubmed-article:19246034 | lifeskim:mentions | umls-concept:C0301625 | lld:lifeskim |
pubmed-article:19246034 | lifeskim:mentions | umls-concept:C0185117 | lld:lifeskim |
pubmed-article:19246034 | pubmed:issue | 1-2 | lld:pubmed |
pubmed-article:19246034 | pubmed:dateCreated | 2009-3-17 | lld:pubmed |
pubmed-article:19246034 | pubmed:abstractText | The molecular action mechanism of MRP, one of the protein kinase C (PKC) substrates, has been under intense investigation, but reports on its role in macrophage function remain controversial. The treatment of macrophage cell lines with bacterial lipopolysaccharide (LPS) induced a high level of MRP expression suggesting that MRP plays a role in the function of activated macrophages. In order to investigate the role of MRP in activated RAW264.7 cells, we stably transfected MRP-specific shRNA expression constructs and tested for alterations in macrophage-related functions. The down-regulation of MRP expression resulted in a marked reduction in chemotaxis toward MCP-1 or extracellular matrix proteins. Furthermore, pharmacological inhibitors of PKC significantly inhibited the chemotaxis in RAW264.7 cells. These data reveals the pivotal role of MRP in the transmigration of activated RAW264.7 cells. | lld:pubmed |
pubmed-article:19246034 | pubmed:language | eng | lld:pubmed |
pubmed-article:19246034 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19246034 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:19246034 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19246034 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19246034 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19246034 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19246034 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19246034 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19246034 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19246034 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19246034 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19246034 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:19246034 | pubmed:issn | 1090-2163 | lld:pubmed |
pubmed-article:19246034 | pubmed:author | pubmed-author:LeeWon-HaWH | lld:pubmed |
pubmed-article:19246034 | pubmed:author | pubmed-author:SukKyounghoK | lld:pubmed |
pubmed-article:19246034 | pubmed:author | pubmed-author:BaeEun MiEM | lld:pubmed |
pubmed-article:19246034 | pubmed:author | pubmed-author:ChunKwang-Rok... | lld:pubmed |
pubmed-article:19246034 | pubmed:author | pubmed-author:KimJae-KwanJK | lld:pubmed |
pubmed-article:19246034 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:19246034 | pubmed:volume | 256 | lld:pubmed |
pubmed-article:19246034 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:19246034 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:19246034 | pubmed:pagination | 92-8 | lld:pubmed |
pubmed-article:19246034 | pubmed:meshHeading | pubmed-meshheading:19246034... | lld:pubmed |
pubmed-article:19246034 | pubmed:meshHeading | pubmed-meshheading:19246034... | lld:pubmed |
pubmed-article:19246034 | pubmed:meshHeading | pubmed-meshheading:19246034... | lld:pubmed |
pubmed-article:19246034 | pubmed:meshHeading | pubmed-meshheading:19246034... | lld:pubmed |
pubmed-article:19246034 | pubmed:meshHeading | pubmed-meshheading:19246034... | lld:pubmed |
pubmed-article:19246034 | pubmed:meshHeading | pubmed-meshheading:19246034... | lld:pubmed |
pubmed-article:19246034 | pubmed:meshHeading | pubmed-meshheading:19246034... | lld:pubmed |
pubmed-article:19246034 | pubmed:meshHeading | pubmed-meshheading:19246034... | lld:pubmed |
pubmed-article:19246034 | pubmed:meshHeading | pubmed-meshheading:19246034... | lld:pubmed |
pubmed-article:19246034 | pubmed:meshHeading | pubmed-meshheading:19246034... | lld:pubmed |
pubmed-article:19246034 | pubmed:meshHeading | pubmed-meshheading:19246034... | lld:pubmed |
pubmed-article:19246034 | pubmed:meshHeading | pubmed-meshheading:19246034... | lld:pubmed |
pubmed-article:19246034 | pubmed:meshHeading | pubmed-meshheading:19246034... | lld:pubmed |
pubmed-article:19246034 | pubmed:meshHeading | pubmed-meshheading:19246034... | lld:pubmed |
pubmed-article:19246034 | pubmed:meshHeading | pubmed-meshheading:19246034... | lld:pubmed |
pubmed-article:19246034 | pubmed:meshHeading | pubmed-meshheading:19246034... | lld:pubmed |
pubmed-article:19246034 | pubmed:meshHeading | pubmed-meshheading:19246034... | lld:pubmed |
pubmed-article:19246034 | pubmed:year | 2009 | lld:pubmed |
pubmed-article:19246034 | pubmed:articleTitle | Suppression of the lipopolysaccharide-induced expression of MARCKS-related protein (MRP) affects transmigration in activated RAW264.7 cells. | lld:pubmed |
pubmed-article:19246034 | pubmed:affiliation | Department of Genetic Engineering, Kyungpook National University, Daegu, Republic of Korea. | lld:pubmed |
pubmed-article:19246034 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:19246034 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
entrez-gene:65108 | entrezgene:pubmed | pubmed-article:19246034 | lld:entrezgene |
entrez-gene:17118 | entrezgene:pubmed | pubmed-article:19246034 | lld:entrezgene |