The importance of murine phospho-MLKL-S345 in situ detection for necroptosis assessment in vivo

Kelepouras, Konstantinos ; Saggau, Julia ; Varanda, Ana Beatriz ; Zrilic, Matea ; Kiefer, Christine ; Rakhsh-Khorshid, Hassan ; Lisewski, Ina ; Uranga-Murillo, Iratxe ; Arias, Maykel ; Pardo, Julian ; Tonnus, Wulf ; Linkermann, Andreas ; Annibaldi, Alessandro ; Walczak, Henning ; Liccardi, Gianmaria

Resumen: Necroptosis is a caspase-independent modality of cell death implicated in many inflammatory pathologies. The execution of this pathway requires the formation of a cytosolic platform that comprises RIPK1 and RIPK3 which, in turn, mediates the phosphorylation of the pseudokinase MLKL (S345 in mouse). The activation of this executioner is followed by its oligomerisation and accumulation at the plasma-membrane where it leads to cell death via plasma-membrane destabilisation and consequent permeabilisation. While the biochemical and cellular characterisation of these events have been amply investigated, the study of necroptosis involvement in vivo in animal models is currently limited to the use of Mlkl−/− or Ripk3−/− mice. Yet, even in many of the models in which the involvement of necroptosis in disease aetiology has been genetically demonstrated, the fundamental in vivo characterisation regarding the question as to which tissue(s) and specific cell type(s) therein is/are affected by the pathogenic necroptotic death are missing. Here, we describe and validate an immunohistochemistry and immunofluorescence-based method to reliably detect the phosphorylation of mouse MLKL at serine 345 (pMLKL-S345). We first validate the method using tissues derived from mice in which Caspase-8 (Casp8) or FADD are specifically deleted from keratinocytes, or intestinal epithelial cells, respectively. We next demonstrate the presence of necroptotic activation in the lungs of SARS-CoV-infected mice and in the skin and spleen of mice bearing a Sharpin inactivating mutation. Finally, we exclude necroptosis occurrence in the intestines of mice subjected to TNF-induced septic shock. Importantly, by directly comparing the staining of pMLKL-345 with that of cleaved Caspase-3 staining in some of these models, we identify spatio-temporal and functional differences between necroptosis and apoptosis supporting a role of RIPK3 in inflammation independently of MLKL versus the role of RIPK3 in activation of necroptosis.

Idioma: Inglés

DOI: 10.1038/s41418-024-01313-6

Año: 2024

Publicado en: Cell Death and Differentiation 31, 7 (2024), 897-909
ISSN: 1350-9047

Factor impacto JCR: 15.4 (2024)

Categ. JCR: CELL BIOLOGY rank: 13 / 204 = 0.064 (2024) - Q1 - T1
Categ. JCR: BIOCHEMISTRY & MOLECULAR BIOLOGY rank: 8 / 319 = 0.025 (2024) - Q1 - T1

Factor impacto SCIMAGO: 4.866 - Molecular Biology (Q1) - Cell Biology (Q1)

Financiación: info:eu-repo/grantAgreement/ES/AEI/PID2020-113963RB-I00
Financiación: info:eu-repo/grantAgreement/ES/DGA/B29-23R
Financiación: info:eu-repo/grantAgreement/ES/ISCIII/CB21-13-00087

Tipo y forma: Artículo (Versión definitiva)