Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2005-5-17
pubmed:abstractText
Microvessels are composed of two types of cells, endothelial cells and pericytes. Pericyte loss or dysfunction participates in various types of disorders, including diabetic retinopathy. Recently, decreased levels of pigment epithelium-derived factor (PEDF) in the eye have been found to predict progression of diabetic retinopathy. However, the effect of PEDF on pericyte growth remains to be unknown. In this study, we investigated whether or how PEDF could stimulate proliferation of cultured retinal pericytes. PEDF stimulated DNA synthesis in pericytes in a dose-dependent manner. PEDF up-regulated pericyte mRNA levels of platelet-derived growth factor-B (PDGF-B). Down-regulation of PDGF-B gene expression by small interfering RNAs completely inhibited the PEDF-induced DNA synthesis in pericytes. Furthermore, PEDF increased protein kinase C (PKC) activity in pericytes and staurosporine, a potent cell-permeable inhibitor of PKC, completely blocked the PDGF-B gene induction and subsequent increase in DNA synthesis in PEDF-exposed pericytes. These results demonstrate that PEDF promotes the growth of cultured pericytes possibly through autocrine production of PDGF-B via PKC activation. Our present study suggests that PEDF could act as a mitogen or survival factor for pericytes, thereby being involved in the maintenance of retinal microvascular homeostasis.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0026-2862
pubmed:author
pubmed:issnType
Print
pubmed:volume
69
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
128-34
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:15896354-Animals, pubmed-meshheading:15896354-Autocrine Communication, pubmed-meshheading:15896354-Base Sequence, pubmed-meshheading:15896354-Blood Platelets, pubmed-meshheading:15896354-Cattle, pubmed-meshheading:15896354-Cell Proliferation, pubmed-meshheading:15896354-Cells, Cultured, pubmed-meshheading:15896354-DNA, pubmed-meshheading:15896354-Dose-Response Relationship, Drug, pubmed-meshheading:15896354-Enzyme Activation, pubmed-meshheading:15896354-Enzyme Inhibitors, pubmed-meshheading:15896354-Eye Proteins, pubmed-meshheading:15896354-Gene Expression Regulation, pubmed-meshheading:15896354-Molecular Sequence Data, pubmed-meshheading:15896354-Nerve Growth Factors, pubmed-meshheading:15896354-Pericytes, pubmed-meshheading:15896354-Platelet-Derived Growth Factor, pubmed-meshheading:15896354-Protein Kinase C, pubmed-meshheading:15896354-RNA, Messenger, pubmed-meshheading:15896354-RNA, Small Interfering, pubmed-meshheading:15896354-Retina, pubmed-meshheading:15896354-Sequence Homology, Nucleic Acid, pubmed-meshheading:15896354-Serpins, pubmed-meshheading:15896354-Staurosporine, pubmed-meshheading:15896354-Transcriptional Activation
pubmed:year
2005
pubmed:articleTitle
Pigment epithelium-derived factor (PEDF) promotes growth of pericytes through autocrine production of platelet-derived growth factor-B.
pubmed:affiliation
Department of Internal Medicine III, Kurume University School of Medicine, 67 Asahi-machi, Kurume 830-0011, Japan. shoichi@med.kurume-u.ac.jp
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't