Lower active force generation and improved fatigue resistance in skeletal muscle from desmin defficient mice

被引:26
作者
Balogh, J
Li, Z
Paulin, D
Arner, A
机构
[1] Lund Univ, Dept Physiol Sci, SE-22184 Lund, Sweden
[2] Univ Paris 07, F-75221 Paris 05, France
关键词
D O I
10.1023/A:1027353930229
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The mechanical effects of the intermediate. lament protein desmin was examined in desmin deficient mice (Des-/-) and their wild type control ( Des +/+). Active force generation was determined in intact soleus muscles and in skinned single fibres from soleus and psoas. A decreased force generation of skinned muscle fibres from Des-/- mice and a tendency towards decreased active force in intact soleus muscle were detected. Concentrations of the contractile protein actin and myosin were not altered in Des-/- muscles. Ca2+-sensitivity of skinned single fibres in Des-/- muscles was unchanged compared to Des+/+. Using a protocol with repeated short tetani an increased fatigue resistance was found in the intact soleus muscles from Des-/- mice. In conclusion, desmin intermediate. laments are required for optimal generation or transmission of active force in skeletal muscle. Although other studies have shown that the desmin intermediate. laments appear to influence Ca2+-handling, the Ca2+-sensitivity of the contractile. laments is not altered in skeletal muscle of Des-/- mice. Previous studies have reported a switch towards slower myosin isoforms in slow skeletal muscle of Des-/- mice. The increased fatigue resistance show that this change is reflected in the physiological function of the muscle.
引用
收藏
页码:453 / 459
页数:7
相关论文
共 33 条
[11]   The role of the cytoskeleton in heart failure [J].
Hein, S ;
Kostin, S ;
Heling, A ;
Maeno, Y ;
Schaper, J .
CARDIOVASCULAR RESEARCH, 2000, 45 (02) :273-278
[12]   Study of regulation of mitochondrial respiration in vivo An analysis of influence of ADP diffusion and possible role of cytoskeleton [J].
Kay, L ;
Li, ZL ;
Mericskay, M ;
Olivares, J ;
Tranqui, L ;
Fontaine, E ;
Tiivel, T ;
Sikk, P ;
Kaambre, T ;
Samuel, JL ;
Rappaport, L ;
Usson, Y ;
Leverve, X ;
Paulin, D ;
Saks, VA .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1997, 1322 (01) :41-59
[13]   Mechanical properties and structure of carotid arteries in mice lacking desmin [J].
Lacolley, P ;
Challande, P ;
Boumaza, S ;
Cohuet, G ;
Laurent, S ;
Boutouyrie, P ;
Grimaud, JA ;
Paulin, D ;
Lamazière, JMD ;
Li, ZL .
CARDIOVASCULAR RESEARCH, 2001, 51 (01) :178-187
[15]  
LAZARIDES E, 1981, COLD SPRING HARB SYM, V46, P351
[16]   Desmin mutation responsible for idiopathic dilated cardiomyopathy [J].
Li, DX ;
Tapscoft, T ;
Gonzalez, O ;
Burch, PE ;
Quiñones, MA ;
Zoghbi, WA ;
Hill, R ;
Bachinski, LL ;
Mann, DL ;
Roberts, R .
CIRCULATION, 1999, 100 (05) :461-464
[17]   Cardiovascular lesions and skeletal myopathy in mice lacking desmin [J].
Li, ZL ;
ColucciGuyon, E ;
PinconRaymond, M ;
Mericskay, M ;
Pournin, S ;
Paulin, D ;
Babinet, C .
DEVELOPMENTAL BIOLOGY, 1996, 175 (02) :362-366
[18]   Desmin is essential for the tensile strength and integrity of myofibrils but not for myogenic commitment, differentiation, and fusion of skeletal muscle [J].
Li, ZL ;
Mericskay, M ;
Agbulut, O ;
ButlerBrowne, G ;
Carlsson, L ;
Thornell, LE ;
Babinet, C ;
Paulin, D .
JOURNAL OF CELL BIOLOGY, 1997, 139 (01) :129-144
[19]   Selective microvascular dysfunction in mice lacking the gene encoding for desmin [J].
Loufrani, L ;
Matrougui, K ;
Li, ZL ;
Lévy, BI ;
Lacolley, P ;
Paulin, D ;
Henrion, D .
FASEB JOURNAL, 2001, 15 (13) :117-+
[20]   The absence of desmin leads to cardiomyocyte hypertrophy and cardiac dilation with compromised systolic function [J].
Milner, DJ ;
Taffet, GE ;
Wang, XJ ;
Pham, T ;
Tamura, T ;
Hartley, C ;
Gerdes, AM ;
Capetanaki, Y .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1999, 31 (11) :2063-2076