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An Immunohistochemical Atlas of Necroptotic Pathway Expression

Shene Chiou, Aysha H. Al-AniJames M. Murphy,Andre L. Samson

EMBO molecular medicine(2024)SCI 1区

Walter & Eliza Hall Inst Med Res | Weill Cornell Med Coll

Cited 1|Views46
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.
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Key words
IBD,Necroptosis,Immunohistochemistry,RIPK3,MLKL
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要点】:该论文提供了一种自动免疫组织化学检测方法,以检测形成固定的小鼠和人体组织中的核凋亡通路调控因子,发现了组织内蛋白表达的异质性,揭示了在疾病背景下核凋亡通路失调的情况。

方法】:利用自动化免疫组织化学检测方法,检测形成固定的小鼠和人体组织中的核凋亡调控因子。

实验】:观察到组织内蛋白表达的异质性,且对于免疫屏障细胞和长寿细胞的表达存在差异。对于无菌炎症、菌群失调或免疫挑战等刺激的响应中,观察到核凋亡调控因子表达的局部变化,与疾病背景下核凋亡通路失调相一致。该方法将有助于在体内精确定位和评估核凋亡信号传导。