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Defective N-sulfation of heparan sulfate proteoglycans limits PDGF-BB binding and pericyte recruitment in vascular development

Abramsson, Alexandra, 1973 (author)
Kurup, Sindhulakshmi (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Busse, Marta (author)
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Yamada, Shuhei (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Lindblom, Per (author)
Schallmeiner, Edith (author)
Uppsala universitet,Institutionen för genetik och patologi
Stenzel, Denise (author)
Sauvaget, Dominique (author)
Ledin, Johan (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Ringvall, Maria (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Landegren, Ulf (author)
Uppsala universitet,Institutionen för genetik och patologi
Kjellén, Lena (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Bondjers, Göran, 1944 (author)
Gothenburg University,Göteborgs universitet,Wallenberglaboratoriet,Wallenberg Laboratory
Li, Jin-Ping (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Lindahl, Ulf (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Spillmann, Dorothe (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Betsholtz, Christer, 1959 (author)
Karolinska Institutet
Gerhardt, Holger, 1969 (author)
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 (creator_code:org_t)
2007-02-08
2007
English.
In: GENES & DEVELOPMENT. - : Cold Spring Harbor Laboratory. - 0890-9369 .- 1549-5477. ; 21:3, s. 316-331
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • During vascular development, endothelial platelet-derived growth factor B (PDGF-B) is critical for pericyte recruitment. Deletion of the conserved C-terminal heparin-binding motif impairs PDGF-BB retention and pericyte recruitment in vivo, suggesting a potential role for heparan sulfate (HS) in PDGF-BB function during vascular development. We studied the participation of HS chains in pericyte recruitment using two mouse models with altered HS biosynthesis. Reduction of N-sulfation due to deficiency in N-deacetylase/N-sulfotransferase-1 attenuated PDGF-BB binding in vitro, and led to pericyte detachment and delayed pericyte migration in vivo. Reduced N-sulfation also impaired PDGF-BB signaling and directed cell migration, but not proliferation. In contrast, HS from glucuronyl C5-epimerase mutants, which is extensively N- and 6-O-sulfated, but lacks 2-O-sulfated L-iduronic acid residues, retained PDGF-BB in vitro, and pericyte recruitment in vivo was only transiently delayed. These observations were supported by in vitro characterization of the structural features in HS important for PDGF-BB binding. We conclude that pericyte recruitment requires HS with sufficiently extended and appropriately spaced N-sulfated domains to retain PDGF-BB and activate PDGF receptor β (PDGFRβ) signaling, whereas the detailed sequence of monosaccharide and sulfate residues does not appear to be important for this interaction.

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)
NATURVETENSKAP  -- Biologi -- Genetik (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Genetics (hsv//eng)

Keyword

smooth-muscle-cells
growth-factor
diabetic-retinopathy
neonatal lethality
mouse-brain
a-chain
mice
identification
deficient
domain
PDGF-B
MEDICINE

Publication and Content Type

ref (subject category)
art (subject category)

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