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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.

Bondjers, Cecilia, 1974 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicinsk och fysiologisk kemi,Institute of Medical Biochemistry
Kalén, Mattias (författare)
Hellström, Mats (författare)
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Scheidl, Stefan Johannes, 1972 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicinsk och fysiologisk kemi,Institute of Medical Biochemistry
Abramsson, Alexandra, 1973 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicinsk och fysiologisk kemi,Institute of Medical Biochemistry
Renner, Oliver (författare)
Lindahl, Per, 1967 (författare)
Gothenburg University,Göteborgs universitet,Wallenberglaboratoriet,Institutionen för medicinsk och fysiologisk kemi,Wallenberg Laboratory,Institute of Medical Biochemistry
Cho, Hyeseon (författare)
Kehrl, John (författare)
Betsholtz, Christer, 1959 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicinsk och fysiologisk kemi,Institute of Medical Biochemistry
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 (creator_code:org_t)
2003
2003
Engelska.
Ingår i: The American journal of pathology. - 0002-9440. ; 162:3, s. 721-9
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • 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.

Nyckelord

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

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