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Am J Physiol Cell Physiol 287: C1763-C1768, 2004. First published August 25, 2004; doi:10.1152/ajpcell.00024.2004
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Methods in Cell Physiology

An in vitro model based on cell monolayers grown on the underside of large- pore filters in bicameral chambers for studying thyrocyte-lymphocyte interactions

Valérie Estienne, Nadège Brisbarre, Stéphanie Blanchin, Josée-Martine Durand-Gorde, Pierre Carayon, and Jean Ruf

French Institute of Health and Medical Research (INSERM) Unit 555, Faculté de Médecine Timone, Université de la Méditerranée, Marseille, France

Submitted 15 January 2004 ; accepted in final form 19 August 2004

In the processes underlying thyroid autoimmunity, thyrocytes probably act as antigen-presenting cells exposing T-cell epitopes to intrathyroid lymphocytes. To study the interactions between lymphocytes and thyrocytes, which are arranged in a tight, polarized monolayer, we developed a new in vitro model based on human thyrocytes grown on the underside of a filter placed in a bicameral chamber. Thyrocytes from Graves' disease glands were plated onto the upper face of a 8-µm-pore polyethylene terephthalate culture insert filter placed in the inverted position and grown for 24 h before the insert was returned to the normal position for a week in the cell culture plate wells. Thyrocytes grown in the presence of thyroid stimulating hormone, forming a homogeneous monolayer on the underside of the filter, reached confluence after 8 days in vitro. The cells developed a transepithelial electrical resistance >1,000 {Omega}·cm2, and the ZO-1 tight junction protein showed a junctional pattern of distribution. Thyrocytes showed a polarized pattern of thyroperoxidase and thyroid stimulating hormone receptor expression in the apical and basolateral positions, respectively. They were also found to aberrantly express DR class II human leukocyte antigen and an Fc immunoglobulin receptor (Fc{gamma}RIIB2) in the basolateral and apical positions, respectively. Autologous intrathyroidal T lymphocytes cocultured for 24 h across the filter with the thyrocyte monolayer proliferated and remained in the upper chamber without any leakage occurring through the epithelial barrier, which makes this model particularly suitable for studying the cell-cell interactions involved in antigen processing.

autoimmunity; cell-cell interactions; cell culture procedure; tight junctions



Address for reprint requests and other correspondence: J. Ruf, French Institute of Health and Medical Research (INSERM) Unit 555, Faculté de Médecine Timone, Université de la Méditerranée, 27, Boulevard Jean Moulin, F-13385 Marseille Cedex 5, France (E-mail: Jean.Ruf{at}medecine.univ-mrs.fr)







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