Congenital canine myasthenia gravis: II. Acetylcholine receptor metabolism.

Abstract:

:Acetylcholine receptor (AChR) metabolism was studied in muscle from juvenile and adult dogs with congenital myasthenia gravis (CMG) and their unaffected littermates. Although the amount of AChR in the junctional region of innervated CMG muscle fibers was 25% of normal, or less, denervation of CMG fibers resulted in the appearance of AChR in extrajunctional membranes at as high a concentration as in denervated normal fibers. The rate of degradation of junctional AChR in CMG fibers explanted to organ culture did not differ significantly from normal. In monolayer cultures derived from enzyme-dissociated CMG muscle, myotubes of normal morphology developed, and the synthesis and degradation of AChR did not differ from normal. Addition of sera from dogs with the acquired autoimmune form of MG accelerated the degradation of AChR on cultured myotubes, but CMG dog sera were without effect. These data suggest that the low junctional membrane density of AChR in CMG does not reflect a primary inability of muscle to synthesize AChR, nor an accelerated degradation of AChR in the postsynaptic membrane, but rather a low insertion rate of AChR in the postsynaptic membrane.

journal_name

Muscle Nerve

journal_title

Muscle & nerve

authors

Oda K,Lennon VA,Lambert EH,Palmer AC

doi

10.1002/mus.880070905

subject

Has Abstract

pub_date

1984-11-01 00:00:00

pages

717-24

issue

9

eissn

0148-639X

issn

1097-4598

journal_volume

7

pub_type

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