Your browser doesn't support javascript.
loading
Algorithmic assessment of cellular senescence in experimental and clinical specimens.
Kohli, J; Wang, B; Brandenburg, S M; Basisty, N; Evangelou, K; Varela-Eirin, M; Campisi, J; Schilling, B; Gorgoulis, V; Demaria, M.
Afiliação
  • Kohli J; European Research Institute for the Biology of Ageing (ERIBA), University Medical Center Groningen (UMCG), University of Groningen (RUG), Groningen, the Netherlands.
  • Wang B; European Research Institute for the Biology of Ageing (ERIBA), University Medical Center Groningen (UMCG), University of Groningen (RUG), Groningen, the Netherlands.
  • Brandenburg SM; European Research Institute for the Biology of Ageing (ERIBA), University Medical Center Groningen (UMCG), University of Groningen (RUG), Groningen, the Netherlands.
  • Basisty N; Buck Institute for Research on Aging, Novato, CA, USA.
  • Evangelou K; Molecular Carcinogenesis Group, Department of Histology and Embryology, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
  • Varela-Eirin M; European Research Institute for the Biology of Ageing (ERIBA), University Medical Center Groningen (UMCG), University of Groningen (RUG), Groningen, the Netherlands.
  • Campisi J; Buck Institute for Research on Aging, Novato, CA, USA.
  • Schilling B; Buck Institute for Research on Aging, Novato, CA, USA.
  • Gorgoulis V; Molecular Carcinogenesis Group, Department of Histology and Embryology, Medical School, National and Kapodistrian University of Athens, Athens, Greece. vgorg@med.uoa.gr.
  • Demaria M; Faculty Institute for Cancer Sciences, Manchester Academic Health Sciences Centre, University of Manchester, Manchester, UK. vgorg@med.uoa.gr.
Nat Protoc ; 16(5): 2471-2498, 2021 05.
Article em En | MEDLINE | ID: mdl-33911261
ABSTRACT
The development of genetic tools allowed for the validation of the pro-aging and pro-disease functions of senescent cells in vivo. These discoveries prompted the development of senotherapies-pharmaceutical interventions aimed at interfering with the detrimental effect of senescent cells-that are now entering the clinical stage. However, unequivocal identification and examination of cellular senescence remains highly difficult because of the lack of universal and specific markers. Here, to overcome the limitation of measuring individual markers, we describe a detailed two-phase algorithmic assessment to quantify various senescence-associated parameters in the same specimen. In the first phase, we combine the measurement of lysosomal and proliferative features with the expression of general senescence-associated genes to validate the presence of senescent cells. In the second phase we measure the levels of pro-inflammatory markers for specification of the type of senescence. The protocol can help graduate-level basic scientists to improve the characterization of senescence-associated phenotypes and the identification of specific senescent subtypes. Moreover, it can serve as an important tool for the clinical validation of the role of senescent cells and the effectiveness of anti-senescence therapies.
Assuntos

Texto completo: 1 Temas: ECOS / Aspectos_gerais Bases de dados: MEDLINE Assunto principal: Algoritmos / Técnicas Citológicas / Senescência Celular Tipo de estudo: Guideline Limite: Humans Idioma: En Revista: Nat Protoc Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Temas: ECOS / Aspectos_gerais Bases de dados: MEDLINE Assunto principal: Algoritmos / Técnicas Citológicas / Senescência Celular Tipo de estudo: Guideline Limite: Humans Idioma: En Revista: Nat Protoc Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Holanda