Abstract

Muscle function is determined by its structure and fiber type composition. Here we describe a protocol to examine muscle histology and myofiber types using hematoxylin and eosin (H&E) and immunofluorescence staining, respectively. H&E stain nucleus in blue and cytoplasm in red, therefore allowing for morphological analyses, such as myofiber diameter, the presence of degenerated and regenerated myofibers, and adipocytes and fibrotic cells. Muscle fibers in adult skeletal muscles of rodents are classified into 4 subtypes based on the expression of myosin heavy chain proteins: Myh7 (type I fiber), Myh2 (type IIA fiber), Myh1 (type IIX fiber), Myh4 (type IIB fiber). A panel of monoclonal antibodies can be used to specifically label these muscle fiber subtypes. These protocols are commonly used in the study of muscle development, growth and regeneration (for example: Wang et al., 2015; Nie et al., 2016; Yue et al., 2016; Wang et al., 2017).

Highlights

  • [Background] Skeletal muscle is composed of myocytes, adipocytes, fibroblasts and other cell types

  • The diameter of muscle fiber and the extent of adipocytes and fibrotic area are associated with muscle strength (Yue et al, 2016)

  • Based on the differential metabolic traits and the expression of myosin heavy chain (MyHC) subtypes, myofibers are classified into four types (I, IIa, IIx and IIb)

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Summary

Introduction

[Background] Skeletal muscle is composed of myocytes, adipocytes, fibroblasts and other cell types. Positive charged microscope slides (IMEB, catalog number: B-8255) 6. 2-methylbutane (Fisher Scientific, catalog number: O3551-4) 10. Xylene (Avantor® Performance Materials, Macron, catalog number: 8668) 13. Xylene-based mounting medium (Source Mount, catalog number: 9277722) 14.

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