J Korean Orthop Assoc.  2002 Apr;37(2):281-287.

Myoblast Transfer Therapy on mdxMouse

Affiliations
  • 1Department of Orthopaedic Surgery, Samsung Cheil Hospital, Sungkyunkwan University, School of Medicine, Korea. chee96@samsung.co.kr
  • 2Department of Anatomy, Korea University College of Medicine, Seoul, Korea.

Abstract

PURPOSE: To observe dystrophin formation and histological improvement in dystrophic muscle of mdx mouse after normal myoblast injection.
MATERIALS AND METHODS
Cultured myoblasts from genetically normal rats were injected into the right quadriceps femoris of a 6-week-old mdx mouse (n=9). dPBS was injected into the left quadriceps femoris as a control. One, 2, and 3 months after injection, The control and experimental group were compared histologically and by dystrophin immunostaining.
RESULTS
When compared with controls 3 months postoperatively, quadriceps femoris in the experimental group exhibited greater cross-sectional area and total fiber number, and the experimental animals contained more normal-appearing and less abnormalappearing fibers than the control group. Most of the fibers in the experimental group showed positive results in dystrophin immunostaining, whereas immunostaining of mdx muscle fibers in the control group was completely negative.
CONCLUSION
This study shows that normal myoblast injection improved the muscle architecture histologically and produced dystrophin protein in dystrophic muscle.

Keyword

Muscular dystrophy; Myoblast transfer therapy; mdx mouse

MeSH Terms

Animals
Dystrophin
Mice
Mice, Inbred mdx
Muscular Dystrophies
Myoblasts*
Quadriceps Muscle
Rats
Dystrophin
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