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A protocol for rapid and parallel isolation of myocytes and non-myocytes from multiple mouse hearts

journal contribution
posted on 2024-12-19, 00:07 authored by Gabriella FarrugiaGabriella Farrugia, MA McLellan, KL Weeks, A Matsumoto, Charles Cohen, Crisdion KrstevskiCrisdion Krstevski, Taylah Gaynor, Adam ParslowAdam Parslow, Julie McMullenJulie McMullen, Ruvantha PintoRuvantha Pinto
This protocol features parallel isolation of myocytes and non-myocytes from murine hearts. It was designed with considerations for (1) time required to extract cardiac cells, (2) cell viability, and (3) protocol scalability. Here, a peristaltic pump and 3D-printed elements are combined to perfuse the heart with enzymes to dissociate cells. Myocytes and non-myocytes extracted using this protocol are separated by centrifugation and/or fluorescence-activated cell sorting for use in downstream applications including single-cell omics or other bio-molecular analyses. For complete details on the use and execution of this protocol, please refer to McLellan et al. (2020).

Funding

This work is supported by the National Health and Medical Research Council (Australia) Ideas Grant (GNT1188503) to A.R.P. and in part by the Victorian Government’s Operational Infrastructure Support Program. K.L.W. is supported by a Future Leader Fellowship from the National Heart Foundation of Australia (award ID 102539). J.R.M. is supported by a National Health and Medical Research Council Senior Research Fellowship (ID 1078985).

History

Publication Date

2021-12-17

Journal

STAR Protocols

Volume

2

Issue

4

Article Number

100866

Pagination

18p.

Publisher

Elsevier

ISSN

2666-1667

Rights Statement

© 2021 The Author(s). https://creativecommons.org/licenses/by-nc-nd/4.0/

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