Preparation of mitochondrial damage-associated molecular patterns from mouse liver tissue

Mitochondrial damage-associated molecular patterns (mitoDAMPs) are released from cells dying uncontrolled, non-apoptotic deaths, usually secondary to disease or trauma. Here, we describe preparation of mitoDAMPs from mouse liver, but this protocol can be adapted for preparation of mitoDAMPs from oth...

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Veröffentlicht in:STAR protocols 2022-12, Vol.3 (4), p.101738-101738, Article 101738
Hauptverfasser: Westhaver, Lauren P., Nersesian, Sarah, Nelson, Adam, MacLean, Leah K., Carter, Emily B., Boudreau, Jeanette E.
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Sprache:eng
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Zusammenfassung:Mitochondrial damage-associated molecular patterns (mitoDAMPs) are released from cells dying uncontrolled, non-apoptotic deaths, usually secondary to disease or trauma. Here, we describe preparation of mitoDAMPs from mouse liver, but this protocol can be adapted for preparation of mitoDAMPs from other species and tissues. Tissues are dissociated and then processed to isolate mitochondria. Mitochondria are then sonicated and mitoDAMPs are collected by ultracentrifugation. This procedure produces μg quantities of mitoDAMPs and facilitates research to understand their impacts in health and disease. For complete details on the use and execution of this protocol, please refer to Westhaver et al. (2022). [Display omitted] •Isolation protocol for mitochondrial damage-associated molecular patterns (mitoDAMPs)•Optimized isolation from mouse liver with optional substitution with cultured cells•We describe tissue harvest, mitochondria isolation, and simulated tissue damage•Applicable to study of diseases involving tissue damage, cancer, and necrotic cell death Publisher’s note: Undertaking any experimental protocol requires adherence to local institutional guidelines for laboratory safety and ethics. Mitochondrial damage-associated molecular patterns (mitoDAMPs) are released from cells dying uncontrolled, non-apoptotic deaths, usually secondary to disease or trauma. Here, we describe preparation of mitoDAMPs from mouse liver, but this protocol can be adapted for preparation of mitoDAMPs from other species and tissues. Tissues are dissociated and then processed to isolate mitochondria. Mitochondria are then sonicated and mitoDAMPs are collected by ultracentrifugation. This procedure produces μg quantities of mitoDAMPs and facilitates research to understand their impacts in health and disease.
ISSN:2666-1667
2666-1667
DOI:10.1016/j.xpro.2022.101738