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Examination of Pyroptosis by Flow Cytometry.
Chang, He; Chen, Zhi; Gao, Li; Cao, Hong; Wang, Yongqiang; Zheng, Shijun J.
Affiliation
  • Chang H; National Key Laboratory of Veterinary Public Health Security; Animal Epidemiology of the Ministry of Agriculture; College of Veterinary Medicine, China Agricultural University.
  • Chen Z; National Key Laboratory of Veterinary Public Health Security; Animal Epidemiology of the Ministry of Agriculture; College of Veterinary Medicine, China Agricultural University.
  • Gao L; National Key Laboratory of Veterinary Public Health Security; Animal Epidemiology of the Ministry of Agriculture; College of Veterinary Medicine, China Agricultural University.
  • Cao H; National Key Laboratory of Veterinary Public Health Security; Animal Epidemiology of the Ministry of Agriculture; College of Veterinary Medicine, China Agricultural University.
  • Wang Y; National Key Laboratory of Veterinary Public Health Security; Animal Epidemiology of the Ministry of Agriculture; College of Veterinary Medicine, China Agricultural University.
  • Zheng SJ; National Key Laboratory of Veterinary Public Health Security; Animal Epidemiology of the Ministry of Agriculture; College of Veterinary Medicine, China Agricultural University; sjzheng@cau.edu.cn.
J Vis Exp ; (207)2024 May 31.
Article in En | MEDLINE | ID: mdl-38884484
ABSTRACT
Pyroptosis is an inflammatory type of programmed cell death predominantly driven by the formation of plasma membrane pores by the N-terminus generated from the cleaved Gasdermin (GSDM) family proteins. Examination of membrane-attached GSDM-NT by Western Blot is the most commonly used method for evaluating pyroptosis. However, it is difficult to differentiate cells with pyroptosis from other forms of cell death using this method. In this study, Infectious Bursal Disease Virus (IBDV)-infected DF-1 cells were employed as a model to quantify the proportion of cells undergoing pyroptosis by flow cytometry, utilizing specific antibodies against the N-terminal fragment of chicken GSDME (chGSDME-NT) and propidium iodide (PI) staining. The chGSDME-NT-positive cells were readily detectable by flow cytometry using Alexa Fluor 647-labeled anti-chGSDME-NT antibodies. Moreover, the proportion of chGSDME-NT/PI double-positive cells in IBDV-infected cells (around 33%) was significantly greater than in mock-infected controls (P < 0.001). These findings indicate that examination of membrane-bound chGSDME-NT by flow cytometry is an effective approach for determining pyroptotic cells among cells undergoing cell death.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chickens / Infectious bursal disease virus / Flow Cytometry / Pyroptosis Limits: Animals Language: En Journal: J Vis Exp Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chickens / Infectious bursal disease virus / Flow Cytometry / Pyroptosis Limits: Animals Language: En Journal: J Vis Exp Year: 2024 Document type: Article