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Human fetal xenografts of brainstem tissue containing locus coeruleus neurons: Functional and structural studies of intraocular grafts in athymic nude rats

Research output: Contribution to journal › Article › peer-review

15 Scopus citations

Abstract

Fetal human brainstem tissue including the nucleus locus coeruleus was transplanted to the anterior eye chamber of athymic nude rats. Most transplants survived and grew in the anterior chamber of the eye. After 9-15 months, the host animals were anesthetized and electrophysiological or in vivo electrochemical recordings were performed. The brainstem transplants contained spontaneously active neurons with regular single-spike firing patterns. The neurons responded to ipsilateral light stimulation with an increase in firing rate and to the α2-receptor agonist clonidine with significantly decreased firing rates. In vivo electrochemical studies demonstrated reproducible noradrenergic overflow after local application of potassium. Immunohistochemical evaluation of the brainstem transplants showed an abundance of tyrosine hydroxylase-positive neurons and neurites in all transplants and a dense network of neurofilament-, synapsin-, and glial fibrillary acidic protein-positive profiles throughout the grafts. Taken together, the present physiological and histochemical data indicate that it is possible to obtain transplants containing a specific monoaminergic population within the brainstem from human fetal fragments and to maintain these transplants in oculo in athymic nude rats for at least 15 months, during which time noradrenergic neurons develop.

Original languageEnglish
Pages (from-to)7-17
Number of pages11
JournalExperimental Neurology
Volume118
Issue number1
DOIs
StatePublished - Oct 1992

Bibliographical note

Funding Information:
Thanks are due to Ms. Ludmila Mackerlova for expert technical help. This paper was supported by the Swedish Medical Research Council, Grants 8650,8868, and 9917, Magnus Bergvall, Lars Hierta, and Karolinska Institute Foundations, as well as USPHS Grants AGO6434 and AG00441.

Funding

Thanks are due to Ms. Ludmila Mackerlova for expert technical help. This paper was supported by the Swedish Medical Research Council, Grants 8650,8868, and 9917, Magnus Bergvall, Lars Hierta, and Karolinska Institute Foundations, as well as USPHS Grants AGO6434 and AG00441.

FundersFunder number
Karolinska Institute Foundations
Magnus Bergvall
National Institute on AgingR23AG006434
U.S. Public Health ServiceAG00441, AGO6434
Medicinska Forskningsrådet8650,8868, 9917

    ASJC Scopus subject areas

    • Neurology
    • Developmental Neuroscience

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