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  • 1
    ISSN: 1432-1106
    Keywords: Platelet-derived growth factor ; Receptors ; Facial nerve ; Immunohistochemistry ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We investigated the expression of platelet-derived growth factor (PDGF) and its receptors in rat facial nuclei following axotomy by in situ hybridization and immunohistochemistry. Facial nuclei were examined on days 3, 6, 12, 19 and 26 postoperatively (p.o.). Strong immunoreactivity for PDGF was found in facial neurons and surrounding astrocytes on the ipsilateral side of the brainstem already after 3 days p.o. and persisted at a high level until day 26 p.o. in rats with a facial nerve cut injury. After crushing of the facial nerve, a similar increase was seen in PDGF immunoreactivity which, however, decreased after day 19 p.o., when reinnervation had occurred. Reactive gliosis appeared on the operated side and was confirmed by an increase in intensity of GFAP staining. The kinetics of PDGF A-chain mRNA expression corresponded to the PDGF immunoreactivity, whereas the B-chain mRNA was present only in the neurons. The PDGF α-receptor immunoreactivity as well as the mRNA were detected in scattered glial cells. The density of the PDGF α-receptor mRNA expressing glial cells was higher on the injured side, but the intensity of the expression per cell did not change after axotomy. An increase in PDGF β-receptor immunoreactivity was seen in the ipsilateral facial nuclei after 3–6 days p.o., however, the increase in the mRNA could not be detected. The staining persisted until day 26 p.o., when transected facial neurons showed heavier staining than those that had been crushed. Furthermore, both mRNA and protein of the β-receptor were expressed in the blood vessels after 3–6 days p.o., increasing with time. These results imply a role for PDGF in the regeneration process following nerve injury.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neuro-oncology 9 (1990), S. 201-210 
    ISSN: 1573-7373
    Keywords: clonogenic survival ; cultured cells ; EGF ; EGF-receptor ; epidermal growth factor ; glioma ; iodine ; radiation effects
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Malignant glioma cells often have more epidermal growth factor (EGF) receptors than normal cells and targeting of toxic substances to the receptor might therefore be an attractive therapeutical approach. Radiation effects were analysed on human glioma cells growing as monolayers after exposure to131I-EGF. Unspecific effects were analysed with131I-BSA or after presaturation with nonradioactive EGF. The radiation effects were compared to the effects obtained by external60Co gamma irradiation. Administration of the highest radioactive concentrations, 0.2–0.5 MBq/ml in the culture medium, corresponded, after 20 min incubation, to a binding of about 1.0–2.5 dpm/cell. Such an exposure to131I decays gave effects on cell survival corresponding to about 2.5 Gy of external gamma irradiation. Somewhat less than half of this effect came from the specific bound radioactivity and the rest from nonbound radioactivity. When administrating lower concentrations of radioactivity both the binding and the radiation effects were smaller. The observations showed that it is possible to inactivate cell-proliferation of glioma cells with specific bound131I-EGF. The possibilities to fractionate the treatments and of binding also other toxic agents than131I to the EGF receptor are discussed.
    Type of Medium: Electronic Resource
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