Literature DB >> 9721739

The polarity of choroid plexus epithelial cells in vitro is improved in serum-free medium.

A Hakvoort1, M Haselbach, J Wegener, D Hoheisel, H J Galla.   

Abstract

The influence of culture conditions on the development of normal characteristics of the choroid plexus epithelium has been investigated in vitro with respect to polarity, barrier properties, transport, and secretory activity. Withdrawal of serum supplement in the culture medium of cells grown on filters caused morphologically visible changes by an increased trimming of microvilli at the apical membrane side, which is accompanied by an increased expression of the Na+,K+-ATPase. Moreover cells under serum-free conditions exhibit structural changes in tight junctional zonula occludens protein-1 (ZO-1) organization, a reduced permeability, and a drastically increased electrical resistance from 150 ohms x cm2 in the presence of serum to 1,500 ohms x cm2 after serum withdrawal. Under these conditions, cell monolayers are able to build up a transcellular proton gradient and to secrete fluid into the upper (apical) filter compartment, which is accompanied by a polarized secretion of proteins like transthyretin. Active transport of the dyes fluorescein and phenol red by the organic anion transporter is found to be driven by the Na+,K+-ATPase. We come to the conclusion that removal of serum favors the differentiation process of the plexus epithelium in vitro, which brings the cell culture model closer to the physiological situation in vivo. We present preliminary evidence that epidermal growth factor may be one component in serum preventing the proper in vitro differentiation.

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Year:  1998        PMID: 9721739     DOI: 10.1046/j.1471-4159.1998.71031141.x

Source DB:  PubMed          Journal:  J Neurochem        ISSN: 0022-3042            Impact factor:   5.372


  14 in total

1.  Transmigration of macrophages across the choroid plexus epithelium in response to the feline immunodeficiency virus.

Authors:  Rick B Meeker; D C Bragg; Winona Poulton; Lola Hudson
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2.  Tight junction protein expression and barrier properties of immortalized mouse brain microvessel endothelial cells.

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Journal:  Brain Res       Date:  2006-12-12       Impact factor: 3.252

Review 3.  Fluid and ion transfer across the blood-brain and blood-cerebrospinal fluid barriers; a comparative account of mechanisms and roles.

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Journal:  Fluids Barriers CNS       Date:  2016-10-31

4.  Air-interface condition promotes the formation of tight corneal epithelial cell layers for drug transport studies.

Authors:  J E Chang; S K Basu; V H Lee
Journal:  Pharm Res       Date:  2000-06       Impact factor: 4.200

5.  Impact of manganese on and transfer across blood-brain and blood-cerebrospinal fluid barrier in vitro.

Authors:  Julia Bornhorst; Christoph A Wehe; Sabine Hüwel; Uwe Karst; Hans-Joachim Galla; Tanja Schwerdtle
Journal:  J Biol Chem       Date:  2012-03-28       Impact factor: 5.157

6.  Establishment of an in vitro brain barrier epithelial transport system for pharmacological and toxicological study.

Authors:  Lewis Zhichang Shi; Wei Zheng
Journal:  Brain Res       Date:  2005-09-28       Impact factor: 3.252

7.  Characterization of immortalized choroid plexus epithelial cell lines for studies of transport processes across the blood-cerebrospinal fluid barrier.

Authors:  Juliane Kläs; Hartwig Wolburg; Tetsuya Terasaki; Gert Fricker; Valeska Reichel
Journal:  Cerebrospinal Fluid Res       Date:  2010-08-12

8.  Establishment and characterization of an immortalized Z310 choroidal epithelial cell line from murine choroid plexus.

Authors:  Wei Zheng; Qiuqu Zhao
Journal:  Brain Res       Date:  2002-12-27       Impact factor: 3.252

9.  Choroid plexus epithelial monolayers--a cell culture model from porcine brain.

Authors:  Carsten Baehr; Valeska Reichel; Gert Fricker
Journal:  Cerebrospinal Fluid Res       Date:  2006-12-21

10.  Ocular Drug Delivery; Impact of in vitro Cell Culture Models.

Authors:  Jaleh Barar; Masoud Asadi; Seyed Abdolreza Mortazavi-Tabatabaei; Yadollah Omidi
Journal:  J Ophthalmic Vis Res       Date:  2009-10
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