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PMID: 1732063 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Multipotent neural cell lines can engraft and participate in development of mouse cerebellum.

Cell ·Vol. 68 ·No. 1 ·1992-01-10 ·Pages 33-51

Snyder EY, Deitcher DL, Walsh C, Arnold-Aldea S, Hartwieg EA, Cepko CL

Abstract

Multipotent neural cell lines were generated via retrovirus-mediated v-myc transfer into murine cerebellar progenitor cells. When transplanted back into the cerebellum of newborn mice, these cells integrated into the cerebellum in a nontumorigenic, cytoarchitecturally appropriate manner. Cells from the same clonal line differentiated into neurons or glia in a manner appropriate to their site of engraftment. Engrafted cells, identified by lacZ expression and PCR-mediated detection of a unique sequence arrangement, could be identified in animals up to 22 months postengraftment. Electron microscopic and immunohistochemical analysis demonstrated that some engrafted cells were similar to host neurons and glia. Some transplant-derived neurons received appropriate synapses and formed normal intercellular contacts. These data indicate that generating immortalized cell lines for repair of, or transport of genes into, the CNS may be feasible. Such lines may also provide a model for commitment and differentiation of cerebellar progenitor cells.

Related Genes
MeSH Terms
Aging Animals Biomarkers Brain Tissue Transplantation/physiology Cell Differentiation Cell Line Cerebellum/cytology,growth & development,transplantation Culture Techniques/methods Genes, myc Mice Mice, Inbred Strains Microscopy, Electron Neurons/cytology,transplantation,ultrastructure Transfection beta-Galactosidase/genetics,metabolism
Chemicals
Biomarkers beta-Galactosidase
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Snyder E Y
Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115.
Deitcher D L
Walsh C
Arnold-Aldea S
Hartwieg E A
Cepko C L
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1992-01-10
Pages
33-51
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NINDS NIH HHS · 5-K08-NS01403-02 · United States
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