Molecular evidence for the expression of nicotinic acetylcholine receptor alpha-chain in mouse thymus.

LM Wheatley, D Urso, K Tumas, J Maltzman… - … (Baltimore, Md.: 1950 …, 1992 - journals.aai.org
LM Wheatley, D Urso, K Tumas, J Maltzman, E Loh, AI Levinson
Journal of immunology (Baltimore, Md.: 1950), 1992journals.aai.org
The presence and structure of nicotinic acetylcholine receptor (nAChR) in the thymus has
been a subject of interest for many years because of its possible role in the pathogenesis of
the autoimmune disease myasthenia gravis. Using the polymerase chain reaction with
primers specific for the alpha-chain of nAChR (nAChR-alpha), an 880-bp homologous band
was found after amplification of cDNA prepared from mouse thymus, thymic medullary and
cortical epithelial cell lines, but not from thymocytes or kidney. Sequencing of the …
Abstract
The presence and structure of nicotinic acetylcholine receptor (nAChR) in the thymus has been a subject of interest for many years because of its possible role in the pathogenesis of the autoimmune disease myasthenia gravis. Using the polymerase chain reaction with primers specific for the alpha-chain of nAChR (nAChR-alpha), an 880-bp homologous band was found after amplification of cDNA prepared from mouse thymus, thymic medullary and cortical epithelial cell lines, but not from thymocytes or kidney. Sequencing of the polymerase chain reaction product from the thymus and thymic medullary and cortical epithelial lines showed identity with skeletal muscle nAChR-alpha over the region examined. This region includes the domains of the molecule on which B cell and T cell autoantigenic targets have been described. No evidence was found in mouse tissue for the exon 3A, which has been described in human muscle and the human rhabdomyosarcoma cell line TE671. Our results provide evidence at the RNA level for the expression of the nAChR-alpha on stromal cells but not on thymocytes in normal murine thymus and are consistent with a role for intrathymic autoantigen expression in the pathogenesis of myasthenia gravis.
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