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Cografts of adrenal medulla with C6 glioma cells in rats with 6-hydroxydopamine-induced lesions

  • G. Bing
  • , M. F.D. Notter
  • , J. T. Hansen
  • , C. Kellogg
  • , J. H. Kordower
  • , D. M. Gash

Producción científica: Articlerevisión exhaustiva

39 Citas (Scopus)

Resumen

Amitotic [3H]thymidine-labeled C6 glioma cells, which are known to produce neurotrophic factor(s), were grafted alone and with adrenal chromaffin cells in an attempt to improve chromaffin cell survival and phenotypic differentiation. Long-Evans rats with unilateral 6-hydroxydopamine-induced lesions of the nigrostriatal pathway were divided into four groups: (1) those receiving adrenal medullary cells co-transplanted with C6 glioma cells; (2) those receiving adrenal medullary graft alone; (3) those receiving C6 glioma grafts alone; and (4) those serving as a vehicle control group. All rats were killed one month after transplantation. Immunohistochemical, neurochemical, and autoradiographic methods were used to identify and characterize the grafted cells. Tyrosine hydroxylase-immunoreactive cells were found in all animals that received grafts of the adrenal medulla alone or of adrenal medulla co-transplanted with C6 glioma cells. The cograft recipients had more tyrosine hydroxylase-immunoreactive cells than the hosts receiving just adrenal chromaffin cells (P < 0.05). Additionally, more grafted chromaffin cells formed processes in the former group. All three tissue recipient groups (adrenal medullary, C6 glioma cell, and cografted animals) had a significant reduction (P < 0.05) in ipsilateral rotations after amphetamine (0.5 mg/kg i.p.) injections as compared to the control vehicle recipient group. Moreover, the reduction in rotation was more marked in the cografted hosts than in the other two implanted groups (P < 0.05). Significantly higher dopamine levels were found in the transplant sites of both cograft and adrenal medullary graft recipients than in sham grafted control animals.

Idioma originalEnglish
Páginas (desde-hasta)687-697
Número de páginas11
PublicaciónNeuroscience
Volumen34
N.º3
DOI
EstadoPublished - 1990

Financiación

FinanciadoresNúmero del financiador
National Institute of Neurological Disorders and StrokeP01NS025778

    ASJC Scopus subject areas

    • General Neuroscience

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