Literature DB >> 9215731

Response of Schwann cells to mitogens in vitro is determined by pre-exposure to serum, time in vitro, and developmental age.

Z Dong1, C Dean, J E Walters, R Mirsky, K R Jessen.   

Abstract

We compared the mitogenic response of Schwann cells freshly isolated from adult, neonatal, and embryonic nerves, and compared these cells with cells that had been cultured in serum for 5 days. DNA synthesis in response to growth factors was measured using bromodeoxyuridine and immunocytochemistry. Freshly isolated adult Schwann cells were unresponsive to growth factors with or without forskolin to elevate intracellular cAMP levels. After 5 days of culture in serum, or alternatively in defined medium containing fibroblast growth factor 2 plus forskolin, or neu-differentiation factor beta2, adult cells were responsive to mitogens, whereas cells cultured in defined medium alone remained unresponsive. Serum also increased expression of type 1 fibroblast growth factor receptor. Freshly isolated embryonic and neonatal Schwann cells in contrast responded to growth factors even in the absence of forskolin. This responsiveness changed with time in culture. Neonatal cells cultured for 5 days in defined medium in the presence or absence of serum no longer responded to FGF alone, but required forskolin for a mitogenic response. Thus, the response of freshly isolated cells to mitogens is developmentally regulated; extrinsic signals are required to render adult cells responsive to mitogens; and with time in culture, neonatal cells develop a requirement for cAMP elevation for mitogenic response.

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Year:  1997        PMID: 9215731

Source DB:  PubMed          Journal:  Glia        ISSN: 0894-1491            Impact factor:   7.452


  11 in total

1.  Developing Schwann cells acquire the ability to survive without axons by establishing an autocrine circuit involving insulin-like growth factor, neurotrophin-3, and platelet-derived growth factor-BB.

Authors:  C Meier; E Parmantier; A Brennan; R Mirsky; K R Jessen
Journal:  J Neurosci       Date:  1999-05-15       Impact factor: 6.167

2.  N-cadherin mediates axon-aligned process growth and cell-cell interaction in rat Schwann cells.

Authors:  Ina B Wanner; Patrick M Wood
Journal:  J Neurosci       Date:  2002-05-15       Impact factor: 6.167

3.  Non-antagonistic relationship between mitogenic factors and cAMP in adult Schwann cell re-differentiation.

Authors:  Paula V Monje; Sayuri Rendon; Gagani Athauda; Margaret Bates; Patrick M Wood; Mary Bartlett Bunge
Journal:  Glia       Date:  2009-07       Impact factor: 7.452

4.  FAK is required for Schwann cell spreading on immature basal lamina to coordinate the radial sorting of peripheral axons with myelination.

Authors:  Matthew Grove; Peter J Brophy
Journal:  J Neurosci       Date:  2014-10-01       Impact factor: 6.167

5.  Transforming growth factor beta (TGFbeta) mediates Schwann cell death in vitro and in vivo: examination of c-Jun activation, interactions with survival signals, and the relationship of TGFbeta-mediated death to Schwann cell differentiation.

Authors:  D B Parkinson; Z Dong; H Bunting; J Whitfield; C Meier; H Marie; R Mirsky; K R Jessen
Journal:  J Neurosci       Date:  2001-11-01       Impact factor: 6.167

6.  FGF/heparin differentially regulates Schwann cell and olfactory ensheathing cell interactions with astrocytes: a role in astrocytosis.

Authors:  Alessandra Santos-Silva; Richard Fairless; Margaret C Frame; Paul Montague; George M Smith; Andrew Toft; John S Riddell; Susan C Barnett
Journal:  J Neurosci       Date:  2007-07-04       Impact factor: 6.167

7.  TGFbeta type II receptor signaling controls Schwann cell death and proliferation in developing nerves.

Authors:  Maurizio D'Antonio; Anna Droggiti; M Laura Feltri; Jürgen Roes; Lawrence Wrabetz; Rhona Mirsky; Kristján R Jessen
Journal:  J Neurosci       Date:  2006-08-16       Impact factor: 6.167

8.  Pre-degenerated peripheral nerves co-cultured with bone marrow-derived cells: a new technique for harvesting high-purity Schwann cells.

Authors:  Xiao-Pan Wang; Min Wu; Jian-Zhong Guan; Zhao-Dong Wang; Xu-Bin Gao; Yang-Yang Liu
Journal:  Neural Regen Res       Date:  2016-10       Impact factor: 5.135

9.  Expression and localization of Ski determine cell type-specific TGFbeta signaling effects on the cell cycle.

Authors:  Claire Jacob; Henrik Grabner; Suzana Atanasoski; Ueli Suter
Journal:  J Cell Biol       Date:  2008-08-11       Impact factor: 10.539

10.  Nlrp6 promotes recovery after peripheral nerve injury independently of inflammasomes.

Authors:  Elke Ydens; Dieter Demon; Guillaume Lornet; Vicky De Winter; Vincent Timmerman; Mohamed Lamkanfi; Sophie Janssens
Journal:  J Neuroinflammation       Date:  2015-08-08       Impact factor: 8.322

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