Topic
Skeletal muscle
About: Skeletal muscle is a research topic. Over the lifetime, 58810 publications have been published within this topic receiving 2469678 citations. The topic is also known as: skeletal muscle & striated voluntary muscle.
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01 Jul 1981TL;DR: This chapter discusses the mechanics of Erythrocytes, Leukocytes, and Other Cells, and their role in Bone and Cartilage, and the properties of Bioviscoelastic Fluids, which are a by-product of these cells.
Abstract: Prefaces. 1. Introduction: A sketch of the History and Scope of the Field. 2. The Meaning of the Constitutive Equation. 3. The Flow Properties of Blood. 4. Mechanics of Erythrocytes, Leukocytes, and Other Cells. 5. Interaction of Red Blood Cells with Vessel Wall, and Wall Shear with Endothelium. 6 Bioviscoelastic Fluids. Bioviscoelastic Solids. 8. Mechanical Properties and Active Remodeling of Blood Vessels. 9. Skeletal Muscle. 10. Heart Muscle. 11. Smooth Muscles. 12. Bone and Cartilage. Indices
6,027 citations
TL;DR: RNA and DNA expression vectors containing genes for chloramphenicol acetyltransferase, luciferase, and beta-galactosidase were separately injected into mouse skeletal muscle in vivo and expression was comparable to that obtained from fibroblasts transfected in vitro under optimal conditions.
Abstract: RNA and DNA expression vectors containing genes for chloramphenicol acetyltransferase, luciferase, and beta-galactosidase were separately injected into mouse skeletal muscle in vivo. Protein expression was readily detected in all cases, and no special delivery system was required for these effects. The extent of expression from both the RNA and DNA constructs was comparable to that obtained from fibroblasts transfected in vitro under optimal conditions. In situ cytochemical staining for beta-galactosidase activity was localized to muscle cells following injection of the beta-galactosidase DNA vector. After injection of the DNA luciferase expression vector, luciferase activity was present in the muscle for at least 2 months.
4,022 citations
TL;DR: Results suggest that GDF-8 functions specifically as a negative regulator of skeletal muscle growth, which is significantly larger than wild-type animals and show a large and widespread increase in skeletal muscle mass.
Abstract: The transforming growth factor-beta (TGF-beta) superfamily encompasses a large group of growth and differentiation factors playing important roles in regulating embryonic development and in maintaining tissue homeostasis in adult animals. Using degenerate polymerase chain reaction, we have identified a new murine TGF-beta family member, growth/differentiation factor-8 (GDF-8), which is expressed specifically in developing and adult skeletal muscle. During early stages of embryogenesis, GDF-8 expression is restricted to the myotome compartment of developing somites. At later stages and in adult animals, GDF-8 is expressed in many different muscles throughout the body. To determine the biological function of GDF-8, we disrupted the GDF-8 gene by gene targeting in mice. GDF-8 null animals are significantly larger than wild-type animals and show a large and widespread increase in skeletal muscle mass. Individual muscles of mutant animals weigh 2-3 times more than those of wild-type animals, and the increase in mass appears to result from a combination of muscle cell hyperplasia and hypertrophy. These results suggest that GDF-8 functions specifically as a negative regulator of skeletal muscle growth.
3,791 citations
TL;DR: In this article, the authors present a sketch of the history and scope of the field of bio-physiology and discuss the meaning of the Constitutive Equation and the flow properties of blood.
Abstract: Prefaces. 1. Introduction: A sketch of the History and Scope of the Field. 2. The Meaning of the Constitutive Equation. 3. The Flow Properties of Blood. 4. Mechanics of Erythrocytes, Leukocytes, and Other Cells. 5. Interaction of Red Blood Cells with Vessel Wall, and Wall Shear with Endothelium. 6 Bioviscoelastic Fluids. Bioviscoelastic Solids. 8. Mechanical Properties and Active Remodeling of Blood Vessels. 9. Skeletal Muscle. 10. Heart Muscle. 11. Smooth Muscles. 12. Bone and Cartilage. Indices
3,670 citations
TL;DR: Two genes encode ubiquitin ligases that are potential drug targets for the treatment of muscle atrophy, and mice deficient in either MAFbx orMuRF1 were found to be resistant to atrophy.
Abstract: Skeletal muscle adapts to decreases in activity and load by undergoing atrophy. To identify candidate molecular mediators of muscle atrophy, we performed transcript profiling. Although many genes were up-regulated in a single rat model of atrophy, only a small subset was universal in all atrophy models. Two of these genes encode ubiquitin ligases: Muscle RING Finger 1 (MuRF1), and a gene we designate Muscle Atrophy F-box (MAFbx), the latter being a member of the SCF family of E3 ubiquitin ligases. Overexpression of MAFbx in myotubes produced atrophy, whereas mice deficient in either MAFbx or MuRF1 were found to be resistant to atrophy. These proteins are potential drug targets for the treatment of muscle atrophy.
3,174 citations