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PMID: 1752215 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Effects of interleukin-1 and tumor necrosis factor-alpha on astrocytes, microglia, oligodendrocytes, and glial precursors in vitro.

Developmental neuroscience ·Vol. 13 ·No. 3 ·1991-00-00 ·Pages 130-7

Merrill JE

Abstract

Microglia and astrocytes undergo proliferative and differentiative changes in vivo after trauma or diseases such as multiple sclerosis (MS). Oligodendrocytes are destroyed in lesions in MS. Interleukin-1 (IL1) and tumor necrosis factor-alpha (TNF alpha) are involved in inflammation of the central nervous system and are elevated in MS. We have investigated the changes in cell morphology and cell number induced by IL1 and TNF alpha in purified and mixed populations of primary rat brain microglia, astrocytes, oligodendrocytes, and glial precursors. Depending on the target population, proliferation, differentiation, or inhibition of cultured cells was observed. The data also suggest that interactions among cell populations occur and support the hypothesis that IL1 and TNF alpha effects may be indirect, possibly through induction of other factors.

MeSH Terms
Animals Astrocytes/drug effects Biomarkers Brain/cytology Cell Differentiation/drug effects Cell Division/drug effects Cells, Cultured Culture Media, Serum-Free/pharmacology Indomethacin/pharmacology Interleukin-1/pharmacology Neuroglia/drug effects Oligodendroglia/drug effects Rats Recombinant Proteins/pharmacology Stem Cells/drug effects Tumor Necrosis Factor-alpha/pharmacology
Chemicals
Biomarkers Culture Media, Serum-Free Interleukin-1 Recombinant Proteins Tumor Necrosis Factor-alpha Indomethacin
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Merrill J E
Department of Neurology, Reed Neurological Research Center, UCLA School of Medicine.
Article Info
Journal
Developmental neuroscience
Abbr.
Dev Neurosci
ISSN
0378-5866
Published
1991-00-00
Pages
130-7
Language
English
Region
Switzerland
NLM ID
7809375
Subset
IM
Grants
NINDS NIH HHS · R01 NS26983 · United States
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