ULTRASTRUCTURAL LOCALIZATION OF IMMUNE-COMPLEXES (IGG AND C3) AT ENDPLATE IN EXPERIMENTAL AUTO-IMMUNE MYASTHENIA-GRAVIS
ULTRASTRUCTURAL LOCALIZATION OF IMMUNE-COMPLEXES (IGG AND C3) AT ENDPLATE IN EXPERIMENTAL AUTO-IMMUNE MYASTHENIA-GRAVIS
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DOI:
10.1097/00005072-197803000-00008
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发表时间:
1978-01-01
影响因子:
3.2
通讯作者:
LENNON, VA
中科院分区:
文献类型:
--
作者:
SAHASHI, K;ENGEL, AG;LENNON, VA
Rats immunized with purified Torpedo acetylcholine receptor (AChR) plus adjuvants developed chronic experimental autoimmune myasthenia gravis (EAMG) after day 28. Forelimb muscles from EAMG rats 29-103 days after immunization and from control animals were used for the ultrastructural localization of Ig[immunoglobulin]G and C3 [3rd component of complement]. IgG was demonstrated with rabbit anti-rat IgG followed by treatment with peroxidase-labeled staphylococcal protein A. C3 was demonstrated with peroxidase-labeled rabbit anti-rat C3, or with unlabeled rabbit anti-rat C3 followed by peroxidase-labeled protein A. In EAMG rats, IgG and C3 were localized on the terminal expansions of the junctional folds, where AChR is known to be located, and on detached, degenerated parts of the folds in the synaptic space. Background staining was negligible. The findings provide unambiguous evidence for a destructive autoimmune reaction involving the postsynaptic membrane in EAMG, implicate the complement system in this reaction and show that detachment of the tips of the junctional folds is one way by which immune complexes and AChR are eliminated from the postsynaptic membrane. The immuno-electron microscopic findings in chronic EAMG closely resemble those described in human myasthenia gravis.