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Identification of a core set of 58 gene transcripts with broad and specific expression in the microvasculature.

Wallgard, Elisabet (author)
Karolinska Institutet, Institutionen för medicinsk biokemi och biofysik
Larsson, Erik, 1975 (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk kemi och cellbiologi,Wallenberglaboratoriet,Institute of Biomedicine, Department of Medical Biochemistry and Cell Biology,Wallenberg Laboratory
He, Liqun (author)
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Hellström, Mats (author)
Karolinska Institutet, Institutionen för medicinsk biokemi och biofysik
Armulik, Annika (author)
Karolinska Institutet
Nisancioglu, Maya H (author)
Genove, Guillem (author)
Karolinska Institutet
Lindahl, Per, 1967 (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk kemi och cellbiologi,Institutionen för medicin, avdelningen för molekylär och klinisk medicin,Wallenberglaboratoriet,Institute of Biomedicine, Department of Medical Biochemistry and Cell Biology,Institute of Medicine, Department of Molecular and Clinical Medicine,Wallenberg Laboratory
Betsholtz, Christer, 1959 (author)
Karolinska Institutet
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 (creator_code:org_t)
2008
2008
English.
In: Arteriosclerosis, thrombosis, and vascular biology. - 1524-4636 .- 1079-5642. ; 28:8, s. 1469-76
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • OBJECTIVE: Pathological angiogenesis is an integral component of many diseases. Antiangiogenesis and vascular targeting are therefore promising new therapeutic principles. However, few endothelial-specific putative drug targets have been identified, and information is still limited about endothelial-specific molecular processes. Here we aimed at determining the endothelial cell-specific core transcriptome in vivo. METHODS AND RESULTS: Analysis of publicly available microarray data identified a mixed vascular/lung cluster of 132 genes that correlated with known endothelial markers. Filtering against kidney glomerular/nonglomerular and brain vascular/nonvascular microarray profiles separated contaminating lung markers, leaving 58 genes with broad and specific microvascular expression. More than half of these have not previously been linked to endothelial functions or studied in detail before. The endothelial cell-specific expression of a selected subset of these, Eltd1, Gpr116, Ramp2, Slc9a3r2, Slc43a3, Rasip1, and NM_023516, was confirmed by real-time quantitative polymerase chain reaction and/or immunohistochemistry. CONCLUSIONS: We have used a combination of publicly available and own microarray data to identify 58 gene transcripts with broad yet specific expression in microvascular endothelium. Most of these have unknown functions, but many of them are predicted to be cell surface expressed or implicated in cell signaling processes and should therefore be explored as putative microvascular drug targets.

Subject headings

NATURVETENSKAP  -- Biologi -- Bioinformatik och systembiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Bioinformatics and Systems Biology (hsv//eng)
NATURVETENSKAP  -- Biologi -- Annan biologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Other Biological Topics (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Keyword

Animals
Endothelial Cells
Vascular
Gene Expression Profiling

Publication and Content Type

ref (subject category)
art (subject category)

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