Apolipophorin III is dramatically up-regulated during the programmed death of insect skeletal muscle and neurons

1995 ◽  
Vol 26 (1) ◽  
pp. 119-129 ◽  
Author(s):  
Danhui Sun ◽  
Rolf Ziegler ◽  
Carolanne E. Milligan ◽  
Susan Fahrbach ◽  
Lawrence M. Schwartz
1993 ◽  
Vol 158 (2) ◽  
pp. 448-455 ◽  
Author(s):  
Lawrence M. Schwartz ◽  
Margaret E.E. Jones ◽  
Lucy Kosz ◽  
Kiefer Kuah

Author(s):  
Jian Shou ◽  
Xinjuan Shi ◽  
Xiaoguang Liu ◽  
Yingjie Chen ◽  
Peijie Chen ◽  
...  

AbstractImmune cells are involved in skeletal muscle regeneration. The mechanism by which Treg cells are involved in the regeneration of injured skeletal muscle is still unclear. The purpose of this study was to explore the role of programmed death-1 in contused skeletal muscle regeneration, and to clarify the regulation of programmed death-1 on Treg cell generation and macrophage polarization, in order to deepen our understanding of the relationship between the immune system and injured skeletal muscle regeneration. The results show that programmed death-1 knockdown reduced the number of Treg cells and impaired contused skeletal muscle regeneration compared with those of wild-type mice. The number of pro-inflammatory macrophages in the contused skeletal muscle of programmed death-1 knockout mice increased, and the expression of pro-inflammatory factors and oxidative stress factors increased, while the number of anti-inflammatory macrophages and the expression of anti-inflammatory factors, antioxidant stress factors, and muscle regeneration-related factors decreased. These results suggest that programmed death-1 can promote contused skeletal muscle regeneration by regulating Treg cell generation and macrophage polarization.


2017 ◽  
Vol 28 (6) ◽  
pp. 493-509 ◽  
Author(s):  
Megan L. Cramer ◽  
Guohong Shao ◽  
Louise R. Rodino-Klapac ◽  
Louis G. Chicoine ◽  
Paul T. Martin

Abstracts ◽  
1978 ◽  
pp. 643
Author(s):  
R.B. Clark ◽  
K.A.F. Gration ◽  
P.N.R. Usherwood

1984 ◽  
Vol 400 (4) ◽  
pp. 439-441 ◽  
Author(s):  
T. Miyamoto ◽  
Y. Ohizumi ◽  
H. Washio ◽  
Y. Yasumoto

1956 ◽  
Vol 2 (4) ◽  
pp. 131-142 ◽  
Author(s):  
A. J. Hodge

The available evidence from phase contrast, polarization optical, and electron microscopic studies on vertebrate skeletal muscle, insect skeletal muscle, and dipteran flight muscle is interpreted as favoring the following general structure of striated muscle. A continuous array of filaments (actin) runs through all bands of the sarcomere. These are linked by an axially periodic system of transverse filamentous bridges. Myosin (and probably other substances) are localized in the A bands. The system of transverse bridges compensates the birefringence of actin and is thus responsible for the isotropy of the I band. Myosin is responsible for the birefringence of the A bands. On strong contraction, A band material migrates to the Z bands to form contraction bands. It is not yet certain whether this migration involves myosin or another A band component.


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