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PMID: 10364436 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Neuronal differentiation of NT2/D1 teratocarcinoma cells is accompanied by a loss of lamin A/C expression and an increase in lamin B1 expression.

Experimental neurology ·Vol. 157 ·No. 2 ·1999-06-00 ·Pages 241-50

Pierce T, Worman HJ, Holy J

Abstract

Nuclear lamins are prominent elements of the nuclear matrix and are expressed in cell type-specific and differentiation state-specific patterns. A few observations have indicated that nervous tissue may display unusual patterns of lamin expression, in that some neurons appear to lack A-type lamins, which are generally prominently expressed in terminally differentiated, postmitotic cells. To investigate lamin expression patterns during the differentiation of a teratocarcinoma cell line into neurons, NT2/D1 cells were induced to differentiate with retinoic acid treatment. Lamin expression and organization during differentiation in vitro were examined by quantitative immunofluorescence and immunoblotting methods. Undifferentiated NT2/D1 cells were all strongly labeled with an anti-lamin B1 antibody, but displayed marked variation in A/C lamin immunoreactivity. After differentiation, neuronal nuclear envelopes were significantly more strongly labeled by anti-lamin B1 antibody than those of undifferentiated cells, but completely lacked A/C lamin immunoreactivity. In contrast, nonneuronal cells displayed a slight reduction in B1 lamin immunoreactivity, along with a distinct increase in A/C lamin levels. The loss of lamin A/C expression in NT2/D1 neurons is contrary to the pattern normally observed in most somatic cell types during early development and indicates that the nuclear matrix of some neurons, along with certain neuroendocrine and hematopoietic cells, is uniquely specialized in this regard.

MeSH Terms
Cell Differentiation/drug effects Humans Immunohistochemistry Kinetics Lamin Type A Lamin Type B Lamins Neurons/cytology Nuclear Proteins/analysis,biosynthesis Teratocarcinoma/pathology Time Factors Tretinoin/pharmacology Tumor Cells, Cultured
Chemicals
Lamin Type A Lamin Type B Lamins Nuclear Proteins lamin B1 Tretinoin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Pierce T
Department of Anatomy & Cell Biology, School of Medicine, Duluth, Minnesota, 55812-2487, USA.
Worman H J
Holy J
Article Info
Journal
Experimental neurology
Abbr.
Exp Neurol
ISSN
0014-4886
Published
1999-06-00
Pages
241-50
Language
English
Region
United States
NLM ID
0370712
Subset
IM
Grants
NCI NIH HHS · CA66974 · United States
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