Sequence of expression of MyoD1 and various cell surface and cytoskeletal proteins in regenerating mouse muscle fibers following treatment with sodium dihydrogen phosphate

被引:8
作者
Figarella-Branger, D
Pellissier, JF
Bianco, N
Karpati, G
机构
[1] Fac Med Marseille, Lab Biopathol Nerveuse & Musculaire JE 2053, F-13385 Marseille 5, France
[2] McGill Univ, Montreal Neurol Inst, Neuromuscular Res Grp, Montreal, PQ, Canada
关键词
regeneration; MyoD1; NCAM; MHC; desmin; utrophin;
D O I
10.1016/S0022-510X(99)00066-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
An immunohistochemical study was performed in order to evaluate the sequence of expression of various cell surface proteins [neural cell adhesion molecule (NCAM) and its polysialylated isoform, PSA NCAM, and utrophin], cytoskeletal proteins (myosin heavy chain isoforms, desmin) and the transcription factor MyoD1 in regenerating mouse muscle fibers following treatment with sodium dihydrogen phosphate. The sequence of the regeneration process with this new myotoxic agent is similar to that which can be observed with other myotoxic substances (local anaesthetics such as bupivacaine or snake venoms). The results show that NCAM, PSA NCAM and desmin were already present on the first day after injury in the presumptive myoblasts. The highest level of all of these proteins was observed on the third day. At this stage, regenerating muscle fibers also strongly and diffusely expressed myosin heavy chain isoforms and utrophin throughout their sarcolemma, whereas NyoD1 expression was observed in the regenerating myonuclei. PSA NCAM and MyoD1 had gradually disappeared from the muscle fibers by the seventh day, by which time, the expression of the other developmentally regulated proteins had also decreased. On the 21st day after injury, a few fibers still expressed NCAM but not the other proteins. This study first shows that sodium dihydrogen phosphate is a new myotoxic agent that is cheap, widely available and easy to handle. It also establishes the schedule of expression of various developmentally regulated proteins in regenerating mouse muscle fibers. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:106 / 115
页数:10
相关论文
共 41 条
[21]   THE CELLULAR EVENTS OF INJURED MUSCLE REGENERATION DEPEND ON THE NATURE OF THE INJURY [J].
LEFAUCHEUR, JP ;
SEBILLE, A .
NEUROMUSCULAR DISORDERS, 1995, 5 (06) :501-509
[22]   ANTI-MYOSIN HEAVY-CHAIN MONOCLONAL-ANTIBODIES REVEAL 2-IIB (FAST) FIBER SUBTYPES [J].
MARINI, JF ;
PONS, F ;
ANOAL, M ;
LEGER, J ;
LEGER, JJ .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1989, 37 (11) :1721-1729
[23]  
Mauro A, 1979, MUSCLE REGENERATION
[24]   PATHO-PHYSIOLOGY OF MUSCLE-FIBER NECROSIS INDUCED BY BUPIVACAINE HYDROCHLORIDE (MARCAINE) [J].
NONAKA, I ;
TAKAGI, A ;
ISHIURA, S ;
NAKASE, H ;
SUGITA, H .
ACTA NEUROPATHOLOGICA, 1983, 60 (3-4) :167-174
[25]  
PASQUINIGUERIN C, 1995, NEUROSMUSC DISORD, V2, P105
[26]   IMMUNOCYTOCHEMICAL ANALYSIS OF MYOSIN HEAVY-CHAINS IN HUMAN-FETAL SKELETAL-MUSCLES [J].
PONS, F ;
LEGER, JOC ;
CHEVALLAY, M ;
TOME, FMS ;
FARDEAU, M ;
LEGER, JJ .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1986, 76 (2-3) :151-163
[27]   DOES UTROPHIN EXPRESSION IN MUSCLES OF MDX MICE DURING POSTNATAL-DEVELOPMENT FUNCTIONALLY COMPENSATE FOR DYSTROPHIN DEFICIENCY [J].
PONS, F ;
ROBERT, A ;
MARINI, JF ;
LEGER, JJ .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1994, 122 (02) :162-170
[28]  
RANTANEN J, 1995, LAB INVEST, V72, P341
[29]  
ROUGON G, 1986, J BIOL CHEM, V261, P3396
[30]  
ROUGON G, 1993, EUR J CELL BIOL, V61, P197