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Neuropoietic cytokines and activin A differentially regulate the phenotype of cultured sympathetic neurons

Fann, Ming-Ji and Patterson, Paul H. (1994) Neuropoietic cytokines and activin A differentially regulate the phenotype of cultured sympathetic neurons. Proceedings of the National Academy of Sciences of the United States of America, 91 (1). pp. 43-47. ISSN 0027-8424. http://resolver.caltech.edu/CaltechAUTHORS:FANpnas94

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Abstract

A number of cytokines sharing limited sequence homology have been grouped as a family because of partially overlapping biological activities, receptor subunit promiscuity, and the prediction of a shared secondary structure. Since several of these cytokines regulate gene expression and cell number in the nervous and hematopoietic systems, this specific group is termed the neuropoietic cytokine family. Using a reverse transcription-polymerase chain reaction-based assay system for monitoring the expression of multiple phenotypic markers in cultured sympathetic neurons, we present further evidence that, in addition to cholinergic differentiation factor/leukemia inhibitory factor and ciliary neurotrophic factor, oncostatin M, growth promoting activity, interleukin 6, and interleukin 11 belong in this family. In addition, one member of the transforming growth factor beta superfamily, activin A, shares a selective overlap with the neuropoietic family in the spectrum of neuropeptides that it induces in sympathetic neurons. The particular neuropeptides induced by activin A, however, demonstrate that the activity of this cytokine is distinct from that of the neuropoietic family. Twenty-six other cytokines and growth factors were without detectable activity in this assay.


Item Type:Article
Additional Information:Copyright © 1994 by the National Academy of Sciences. Communicated by Norman Davidson, August 31, 1993 (received for review July 2, 1993). We thank Doreen McDowell for help with tissue culture materials and Drs. James Miller, Rae Nishi, Jim Smith, David Shelton, David Gearing, Yu-Chung Yang, Stanley Wolf, Mary Freshney, and Gerry Graham for providing cytokines. We are grateful to Dr. Rae Nishi for providing information concerning GPA and activin A activities before publication. We thank Drs. Lisa Banner, Herman Govan, Zaven Kaprielian, and Manhendra Rao and two reviewers for constructive comments on the manuscript. This project is supported by grants from Amgen and the National Institute of Neurological Disorders and Stroke (Javits Neuroscience Investigator Award) to P.H.P., as well as a Fellowship from the Ministry of Education, Taiwan, Republic of China, to M.-J.F. The publication costs of this article were defrayed in part by page charge payment. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. §1734 solely to indicate this fact.
Subject Keywords:CILIARY NEUROTROPHIC FACTOR; LEUKEMIA-INHIBITORY FACTOR; ONCOSTATIN-M; CHOLINERGIC DIFFERENTIATION; NEUROTRANSMITTER PHENOTYPE; MOLECULAR-CLONING; FACTOR CNTF; EXPRESSION; RAT; CELLS
Record Number:CaltechAUTHORS:FANpnas94
Persistent URL:http://resolver.caltech.edu/CaltechAUTHORS:FANpnas94
Alternative URL:http://www.pnas.org/cgi/content/abstract/91/1/43
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:1578
Collection:CaltechAUTHORS
Deposited By: Tony Diaz
Deposited On:01 Feb 2006
Last Modified:26 Dec 2012 08:45

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