[beta]-Defensin overexpression induces progressive muscle degeneration in mice
Defensins comprise a family of cationic antimicrobial peptides characterized by conserved cysteine residues. They are produced in various organs including skeletal muscle and are identified as key elements in the host defense system as potent effectors. At the same time, defensins have potential rol...
Saved in:
Published in | American Journal of Physiology: Cell Physiology Vol. 292; no. 6; p. C2141 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Bethesda
American Physiological Society
01.06.2007
|
Subjects | |
Online Access | Get full text |
ISSN | 0363-6143 1522-1563 |
Cover
Summary: | Defensins comprise a family of cationic antimicrobial peptides characterized by conserved cysteine residues. They are produced in various organs including skeletal muscle and are identified as key elements in the host defense system as potent effectors. At the same time, defensins have potential roles in the regulation of inflammation and, furthermore, can exert cytotoxic effects on several mammalian cells. Here, we developed transgenic mice overexpressing mouse β-defensin-6 to explore the pathophysiological roles of the defensin family as a novel mediator of inflammatory tissue injury. Unexpectedly, the transgenic mice showed short lifespan, poor growth, and progressive myofiber degeneration with functional muscle impairment, predominant centronucleated myofibers, and elevated serum creatine kinase activity, as seen in human muscular dystrophy. Furthermore, some of the transgenic myofibers showed ... accumulation, which would be related to the myofiber apoptosis of limb-girdle muscular dystrophy type 2A. The present findings may unravel a concealed linkage between the innate immune system and the pathophysiology of degenerative diseases. (ProQuest-CSA LLC: ... denotes formulae/symbols omitted.) |
---|---|
Bibliography: | SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 14 |
ISSN: | 0363-6143 1522-1563 |