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Transcription profiling of platelet-derived growth factor-B-deficient mouse embryos identifies RGS5 as a novel marker for pericytes and vascular smooth muscle cells.

Artikel i vetenskaplig tidskrift
Författare Cecilia Bondjers
Mattias Kalén
Mats Hellström
Stefan Johannes Scheidl
Alexandra Abramsson
Oliver Renner
Per Lindahl
Hyeseon Cho
John Kehrl
Christer Betsholtz
Publicerad i The American journal of pathology
Volym 162
Nummer/häfte 3
Sidor 721-9
ISSN 0002-9440
Publiceringsår 2003
Publicerad vid Wallenberglaboratoriet
Institutionen för medicinsk och fysiologisk kemi
Sidor 721-9
Språk en
Länkar www.ncbi.nlm.nih.gov/entrez/query.f...
Ämnesord Animals, Biological Markers, DNA Fingerprinting, Embryo, Female, GTP-Binding Proteins, genetics, Gene Expression Regulation, Developmental, Immunohistochemistry, In Situ Hybridization, Mice, Mice, Inbred C57BL, Mice, Knockout, Muscle, Smooth, Vascular, cytology, embryology, Oligonucleotide Array Sequence Analysis, Pericytes, cytology, Platelet-Derived Growth Factor, deficiency, genetics, physiology, Pregnancy, RGS Proteins, analysis, genetics, Receptor, Platelet-Derived Growth Factor beta, deficiency, genetics, physiology, Transcription, Genetic
Ämneskategorier Medicin och Hälsovetenskap

Sammanfattning

All blood capillaries consist of endothelial tubes surrounded by mural cells referred to as pericytes. The origin, recruitment, and function of the pericytes is poorly understood, but the importance of these cells is underscored by the severe cardiovascular defects in mice genetically devoid of factors regulating pericyte recruitment to embryonic vessels, and by the association between pericyte loss and microangiopathy in diabetes mellitus. A general problem in the study of pericytes is the shortage of markers for these cells. To identify new markers for pericytes, we have taken advantage of the platelet-derived growth factor (PDGF)-B knockout mouse model, in which developing blood vessels in the central nervous system are almost completely devoid of pericytes. Using cDNA microarrays, we analyzed the gene expression in PDGF-B null embryos in comparison with corresponding wild-type embryos and searched for down-regulated genes. The most down-regulated gene present on our microarray was RGS5, a member of the RGS family of GTPase-activating proteins for G proteins. In situ hybridization identified RGS5 expression in brain pericytes, and in pericytes and vascular smooth muscle cells in certain other, but not all, locations. Absence of RGS5 expression in PDGF-B and PDGFR beta-null embryos correlated with pericyte loss in these mice. Residual RGS5 expression in rare pericytes suggested that RGS5 is a pericyte marker expressed independently of PDGF-B/R beta signaling. With RGS5 as a proof-of-principle, our data demonstrate the usefulness of microarray analysis of mouse models for abnormal pericyte development in the identification of new pericyte-specific markers.

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