Myogenesis in thymic transplants in the severe combined immunodeficient mouse model of myasthenia gravis. Differentiation of thymic myoid cells into striated muscle cells

Item Type:	Article
Title:	Myogenesis in thymic transplants in the severe combined immunodeficient mouse model of myasthenia gravis. Differentiation of thymic myoid cells into striated muscle cells
Creators Name:	Spuler, S. and Marx, A. and Kirchner, T. and Hohlfeld, R. and Wekerle, H.
Abstract:	Thymic myoid cells (TMCs) bearing acetylcholine receptors (AchR) on their surface have a central role in the concept of intrathymic autosensitization in the pathogenesis of myasthenia gravis. In a SCID mouse model of myasthenia gravis, solid pieces of thymuses with lymphofollicular hyperplasia were transplanted into SCID mice. The chimeric mice displayed long-term secretion of anti-AchR antibodies. Here, we traced the fate of TMCs contained in transplanted myasthenia gravis thymuses. Unexpectedly, the number of thymic TMCs in transplanted tissue was slightly higher than in untransplanted thymus. More strikingly, the transplanted TMCs were more highly differentiated than their nontransplanted counterparts. This was demonstrated by a more than 10-fold increase of AchR-main immunogenic region epitopes recognized by monoclonal antibody 198. Some TMCs had even differentiated into striated muscle cells. The abundance of AchRs in human thymic transplants in the SCID mouse model of myasthenia gravis may help to study the mechanisms of autosensitization against the AchR in vivo.
Keywords:	Cell Differentiation, Disease Models, Hyperplasia, Kidney, Lymphoid Tissue, Muscle Fibers, Muscle, Myasthenia Gravis, Severe Combined Immunodeficiency, Thymus Gland, Transplantation, Animals, Mice
Source:	American Journal of Pathology
ISSN:	0002-9440
Publisher:	American Society for Investigative Pathology
Volume:	145
Number:	4
Page Range:	766-770
Date:	October 1994
Official Publication:	http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1887318/
PubMed:	View item in PubMed

Repository Staff Only: item control page