An immunohistochemical atlas of necroptotic pathway expression

Author:

Chiou Shene,Al-Ani Aysha H,Pan YiORCID,Patel Komal M,Kong Isabella Y,Whitehead Lachlan W,Light Amanda,Young Samuel N,Barrios Marilou,Sargeant Callum,Rajasekhar PradeepORCID,Zhu LeahORCID,Hempel Anne,Lin Ann,Rickard James A,Hall Cathrine,Gangatirkar Pradnya,Yip Raymond KHORCID,Cawthorne WayneORCID,Jacobsen Annette VORCID,Horne Christopher R,Martin Katherine RORCID,Ioannidis Lisa JORCID,Hansen Diana SORCID,Day Jessica,Wicks Ian P,Law Charity,Ritchie Matthew E,Bowden Rory,Hildebrand Joanne MORCID,O’Reilly Lorraine AORCID,Silke JohnORCID,Giulino-Roth Lisa,Tsui EllenORCID,Rogers Kelly L,Hawkins Edwin D,Christensen Britt,Murphy James MORCID,Samson André LORCID

Abstract

AbstractNecroptosis is a lytic form of regulated cell death reported to contribute to inflammatory diseases of the gut, skin and lung, as well as ischemic-reperfusion injuries of the kidney, heart and brain. However, precise identification of the cells and tissues that undergo necroptotic cell death in vivo has proven challenging in the absence of robust protocols for immunohistochemical detection. Here, we provide automated immunohistochemistry protocols to detect core necroptosis regulators – Caspase-8, RIPK1, RIPK3 and MLKL – in formalin-fixed mouse and human tissues. We observed surprising heterogeneity in protein expression within tissues, whereby short-lived immune barrier cells were replete with necroptotic effectors, whereas long-lived cells lacked RIPK3 or MLKL expression. Local changes in the expression of necroptotic effectors occurred in response to insults such as inflammation, dysbiosis or immune challenge, consistent with necroptosis being dysregulated in disease contexts. These methods will facilitate the precise localisation and evaluation of necroptotic signaling in vivo.

Funder

DHAC | National Health and Medical Research Council

Kenneth Rainin Foundation

Avant Foundation

Crohn’s and Colitis Australia

University of Melbourne

Publisher

Springer Science and Business Media LLC

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