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Conserved and context-dependent roles for pdgfrb signaling during zebrafish vascular mural cell development

Ando, Koji (author)
Uppsala universitet,Vaskulärbiologi,Nippon Med Sch, Inst Adv Med Sci, Dept Mol Pathophysiol, Bunkyo Ku, Tokyo 1138602, Japan
Shih, Yu-Huan (author)
Univ Massachusetts, Dept Mol Cell & Canc Biol, Med Sch, Worcester, MA 01650 USA
Ebarasi, Lwaki (author)
Karolinska Inst, Dept Med Biochem & Biophys, Div Vasc Biol, Stockholm, Sweden
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Grosse, Ann (author)
Univ Massachusetts, Dept Mol Cell & Canc Biol, Med Sch, Worcester, MA 01650 USA
Portman, Daneal (author)
Univ Massachusetts, Dept Mol Cell & Canc Biol, Med Sch, Worcester, MA 01650 USA
Chiba, Ayano (author)
Natl Cerebral & Cardiovasc Ctr Res Inst, Dept Cell Biol, Suita, Osaka 5648565, Japan
Mattonet, Kenny (author)
Max Planck Inst Heart & Lung Res, Dept Dev Genet, Ludwigstr 43, D-61231 Bad Nauheim, Germany
Gerri, Claudia (author)
Max Planck Inst Heart & Lung Res, Dept Dev Genet, Ludwigstr 43, D-61231 Bad Nauheim, Germany; Francis Crick Inst, Human Embryo & Stem Cell Lab, 1 Midland Rd, London NW1 1AT, England
Stainier, Didier Y. R. (author)
Max Planck Inst Heart & Lung Res, Dept Dev Genet, Ludwigstr 43, D-61231 Bad Nauheim, Germany
Mochizuki, Naoki (author)
Natl Cerebral & Cardiovasc Ctr Res Inst, Dept Cell Biol, Suita, Osaka 5648565, Japan
Fukuhara, Shigetomo (author)
Nippon Med Sch, Inst Adv Med Sci, Dept Mol Pathophysiol, Bunkyo Ku, Tokyo 1138602, Japan
Betsholtz, Christer (author)
Uppsala universitet,Vaskulärbiologi,Karolinska Inst, Dept Med Huddinge MedH, Neo, Campus Flemingsberg,Blickagagen 16,Hiss S,Plan 7, SE-14157 Huddinge, Sweden
Lawson, Nathan D. (author)
Univ Massachusetts, Dept Mol Cell & Canc Biol, Med Sch, Worcester, MA 01650 USA
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 (creator_code:org_t)
Elsevier, 2021
2021
English.
In: Developmental Biology. - : Elsevier. - 0012-1606 .- 1095-564X. ; 479, s. 11-22
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Platelet derived growth factor beta and its receptor, Pdgfrb, play essential roles in the development of vascular mural cells, including pericytes and vascular smooth muscle cells. To determine if this role was conserved in zebrafish, we analyzed pdgfb and pdgfrb mutant lines. Similar to mouse, pdgfb and pdgfrb mutant zebrafish lack brain pericytes and exhibit anatomically selective loss of vascular smooth muscle coverage. Despite these defects, pdgfrb mutant zebrafish did not otherwise exhibit circulatory defects at larval stages. However, beginning at juvenile stages, we observed severe cranial hemorrhage and vessel dilation associated with loss of pericytes and vascular smooth muscle cells in pdgfrb mutants. Similar to mouse, pdgfrb mutant zebrafish also displayed structural defects in the glomerulus, but normal development of hepatic stellate cells. We also noted defective mural cell investment on coronary vessels with concomitant defects in their development. Together, our studies support a conserved requirement for Pdgfrb signaling in mural cells. In addition, these zebrafish mutants provide an important model for definitive investigation of mural cells during early embryonic stages without confounding secondary effects from circulatory defects.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)
NATURVETENSKAP  -- Biologi -- Utvecklingsbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Developmental Biology (hsv//eng)

Keyword

Pdgfrb
Mural cells
Pericytes
Vascular smooth muscle cells
Zebrafish

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