Abstract

In inflammatory myopathies, the self-reactive immune cells involved in muscle aggression have been studied mostly using histological assessment of muscle biopsy sections; this methodology provides the advantage of visualizing and identifying cells within the tissue, but it does not allow further investigation. To gain access to live and isolated cells, many studies utilized blood samples; however, in the absence of biological tools to discriminate the leukocytes associated with the autoimmune process from those that emerged from responses against pathogens, the information observed on circulating immune cells often lacks in specificity, and thus result interpretation may prove difficult. In order to selectively retrieve self-reactive immune cells, we developed a protocol to isolate live leukocytes from human muscle biopsies, which allows for further analysis using a large range of methodologies. The protocol uses enzymatic digestion to release live leukocytes from freshly collected skeletal muscle samples, followed by filtration and separation of the leukocytes from the myocytes by density gradient centrifugation. The isolated cells can be submitted immediately to various analysis strategies to characterize ex vivo the specific cellular and molecular mechanisms responsible for self-directed immune muscle aggression or may be placed in culture for expansion.

Highlights

  • Inflammatory myopathies are a group of chronic conditions that affect skeletal muscles; they involve muscle inflammation, weakness and loss of function

  • The most common types include dermatomyositis (DM), necrotizing autoimmune myopathy (NAM), polymyositis (PM), sporadic inclusion body myositis (IBM) and myositis overlapping with systemic connective tissue disorders [1]

  • We developed a protocol allowing the isolation of live leukocytes from fresh human muscle biopsies

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Summary

Introduction

Inflammatory myopathies are a group of chronic conditions that affect skeletal muscles; they involve muscle inflammation, weakness and loss of function. Our protocol only uses common in inexpensive laboratory consumables and equipment, does not require long training to perform, can be achieved within a few hours, enables obtaining live leukocytes, and the number of cells that may be retrieved only depends on the level of infiltration within the muscle tissue As these cells are invading the diseased tissue, it is likely that they are implicated in autoimmune aggression. Once isolated, these leukocytes can be submitted to a variety of analysis methodologies, including viability assays, functional assays and characterization of their phenotype and molecule content by multi-parameter flow cytometry or cytometry by timeof-flight (CyTOF) analysis, genomic single-cell analysis etc. This protocol will open new opportunities to fully investigate muscle-invading leukocytes and better understand the pathogenic mechanisms

Methods
Step-by-step
Materials
Equipment
Dissection of the Muscle Biopsy
Enzymatic Digestion of the Muscle Tissue
Digestion of the DNA Released in the Medium
Filtration of the Individualized Cells from the Remaining Tissue Aggregates
Separation of Leukocytes from Muscle Fiber Cells
Number of Immune Cells Recovered
Reagents Setup
Full Text
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