Abstract |
1. Myoblasts from expanded primary cultures were implanted into cryodamaged soleus muscles of adult BALB/c mice. One to four months later isometric tension recordings were performed in vitro, and the male donor cells implanted into female hosts were traced on histological sections using a Y-chromosome-specific probe. The muscles were either mildly or severely cryodamaged, which led to reductions in tetanic muscle force to 33% (n = 9 muscles, 9 animals) and 70% (n = 11) of normal, respectively. Reduced forces resulted from deficits in regeneration of muscle tissue as judged from the reduced desmin-positive cross-sectional areas (34 and 66% of control, respectively). 2. Implantation of 10(6) myogenic cells into severely cryodamaged muscles more than doubled muscle tetanic force (to 70% of normal, n = 14), as well as specific force (to 66% of normal). Absolute and relative amount of desmin-positive muscle cross-sectional areas were significantly increased indicating improved microarchitecture and less fibrosis. Newly formed muscle tissue was fully innervated since the tetanic forces resulting from direct and indirect (nerve-evoked) stimulation were equal. Endplates were found on numerous Y-positive muscle fibres. 3. As judged from their position under basal laminae of muscle fibres and the expression of M-cadherin, donor-derived cells contributed to the pool of satellite cells on small- and large-diameter muscle fibres. 4. Myoblast implantation after mild cryodamage and in undamaged muscles had little or no functional or structural effects; in both preparations only a few Y-positive muscle nuclei were detected. It is concluded that myoblasts from expanded primary cultures-unlike permanent cell lines-significantly contribute to muscle regeneration only when previous muscle damage is extensive and loss of host satellite cells is severe.
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Authors | A Irintchev, M Langer, M Zweyer, R Theisen, A Wernig |
Journal | The Journal of physiology
(J Physiol)
Vol. 500 ( Pt 3)
Pg. 775-85
(May 01 1997)
ISSN: 0022-3751 [Print] England |
PMID | 9161990
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Cadherins
- Desmin
- M-cadherin
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Topics |
- Animals
- Cadherins
(biosynthesis)
- Cell Count
- Cell Differentiation
- Cell Transplantation
(physiology)
- Cells, Cultured
- Desmin
(metabolism)
- Female
- Fluorescent Antibody Technique, Direct
- Freezing
- Immunohistochemistry
- In Situ Hybridization
- Isometric Contraction
(physiology)
- Male
- Mice
- Mice, Inbred BALB C
- Muscle Contraction
(physiology)
- Muscle Fibers, Skeletal
(physiology)
- Muscle, Skeletal
(cytology, injuries, physiology)
- Regeneration
(physiology)
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