Literature DB >> 6397876

Isolation and characterization of flat cells, a subpopulation of the embryonic chick retina.

H P Li, J B Sheffield.   

Abstract

When the embryonic neutral retina is dissociated into single cells which are maintained in stationary culture, the neuronal cells associate on the surfaces of a second population which we refer to as flat cells. The flat cells appear in the culture in significant numbers after 2 days and are required for neuronal cell attachment. We have been able to isolate pure flat cells from early cultures of mixed retina cells and have identified several antigens which support the concept that these cells are related to the glia. The cells have been tested by immunofluorescence for glial fibrillary acidic protein and have been found positive. Cell surfaces were labeled by transfer of tritiated galactose from UDP-galactose to endogenous acceptors in the presence of exogenous galactosyl transferase. After SDS-PAGE and fluorography, the surface glycoproteins of flat cells were seen to be significantly different from those of the original retina, and from chick fibroblasts. Immunoelectron microscope studies of detergent-extracted flat cells have demonstrated a complex network of intermediate filaments and actin fibers. We conclude that the flat cells are derived from the glia subpopulation of the retina and have adapted to the tissue culture environment by assuming this configuration. The unique surface properties of flat cells may be related to their role as an intermediate substrate between the neuronal cells and the tissue culture dish.

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Year:  1984        PMID: 6397876     DOI: 10.1016/0040-8166(84)90066-1

Source DB:  PubMed          Journal:  Tissue Cell        ISSN: 0040-8166            Impact factor:   2.466


  8 in total

1.  Emergence of flat cells from glia in stationary cultures of embryonic chick neural retina.

Authors:  M Moyer; F Bullrich; J B Sheffield
Journal:  In Vitro Cell Dev Biol       Date:  1990-11

2.  Mammalian neurons in dissociated cultures form clusters in the presence of retinal pigment epithelium.

Authors:  J F MacDonald; L Brandes; M Deverill; I Mody; M W Salter; E Theriault
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

3.  Steroid hormone receptors activate transcription in glial cells of intact retina but not in primary cultures of retinal glial cells.

Authors:  Y C Li; S Hayes; A P Young
Journal:  J Mol Neurosci       Date:  1997-04       Impact factor: 3.444

4.  Effects of alkaline phosphatase inhibitors on chick neural retinal cell differentiation in vitro: ultracytochemical studies.

Authors:  M Araki; F Sato; T Saito
Journal:  Histochem J       Date:  1987 Oct-Nov

5.  A transcriptional enhancer of the glutamine synthetase gene that is selective for retinal Müller glial cells.

Authors:  Y C Li; D Beard; S Hayes; A P Young
Journal:  J Mol Neurosci       Date:  1995       Impact factor: 3.444

6.  The cytoskeletal network controls c-Jun expression and glucocorticoid receptor transcriptional activity in an antagonistic and cell-type-specific manner.

Authors:  A Oren; A Herschkovitz; I Ben-Dror; V Holdengreber; Y Ben-Shaul; R Seger; L Vardimon
Journal:  Mol Cell Biol       Date:  1999-03       Impact factor: 4.272

7.  Retinal FABP principally localizes to neurons and not to glial cells.

Authors:  P A Sellner
Journal:  Mol Cell Biochem       Date:  1993 Jun 9-23       Impact factor: 3.396

8.  A chick neural retina adhesion and survival molecule is a retinol-binding protein.

Authors:  D Schubert; M LaCorbiere; F Esch
Journal:  J Cell Biol       Date:  1986-06       Impact factor: 10.539

  8 in total

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