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Characterization of neuroprogenitor cells expressing the PDGF beta-receptor within the subventricular zone of postnatal mice.

Ishii, Yoko (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk kemi och cellbiologi,Institute of Biomedicine, Department of Medical Biochemistry and Cell Biology
Matsumoto, Yoshiki, 1971 (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk kemi och cellbiologi,Institute of Biomedicine, Department of Medical Biochemistry and Cell Biology
Watanabe, Rie (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk kemi och cellbiologi,Institute of Biomedicine, Department of Medical Biochemistry and Cell Biology
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Elmi, Muna, 1978 (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk kemi och cellbiologi,Institute of Biomedicine, Department of Medical Biochemistry and Cell Biology
Fujimori, Toshihiko (author)
Nissen, Johan (author)
Cao, Yihai (author)
Karolinska Institutet
Nabeshima, Yo-Ichi (author)
Sasahara, Masakiyo (author)
Funa, Keiko, 1949 (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk kemi och cellbiologi,Institute of Biomedicine, Department of Medical Biochemistry and Cell Biology
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 (creator_code:org_t)
Elsevier BV, 2008
2008
English.
In: Molecular and cellular neurosciences. - : Elsevier BV. - 1095-9327 .- 1044-7431. ; 37:3, s. 507-18
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • We report a considerable number of cells in the ventricular and the subventricular zones (SVZ) of newborn mice to stain positive for the PDGF beta-receptor (PDGFRB). Many of them also stained for nestin and/or GFAP but less frequently for the neuroblast marker doublecortin and for the mitotic marker Ki-67. The SVZ of mice with nestin-Cre conditional deletion of PDGFRB expressed the receptor only on blood vessels and was devoid of any morphological abnormality. PDGFRB(-/-) neurospheres showed a higher rate of apoptosis without any significant decrease in proliferation. They demonstrated reduced capacities of migration and neuronal differentiation in response to not only PDGF-BB but also bFGF. Furthermore, the PDGFR kinase inhibitor STI571 blocked the effects of bFGF in control neurosphere cultures. bFGF increased the activity of the PDGFRB promoter as well as the expression and phosphorylation of PDGFRB. These results suggest the presence of the signaling convergence between PDGF and FGF. PDGFRB is needed for survival, and the effects of bFGF in migration and neural differentiation of the cells may be potentiated by induction of PDGFRB.

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)

Keyword

Analysis of Variance
Animals
Animals
Newborn
Bromodeoxyuridine
metabolism
Cell Differentiation
drug effects
genetics
Cell Movement
drug effects
physiology
Cells
Cultured
Enzyme Inhibitors
pharmacology
Gene Expression
drug effects
physiology
Intermediate Filament Proteins
genetics
metabolism
Ki-67 Antigen
metabolism
Lateral Ventricles
cytology
growth & development
Mice
Mice
Inbred C57BL
Mice
Transgenic
Nerve Tissue Proteins
genetics
metabolism
Neurons
physiology
Piperazines
pharmacology
Pyrimidines
pharmacology
Receptor
Platelet-Derived Growth Factor beta
genetics
metabolism
Stem Cells
metabolism
Transfection
methods

Publication and Content Type

ref (subject category)
art (subject category)

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