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Isolation and high-dimensional phenotyping of gastrointestinal immune cells.
David, Bruna A; Rubino, Stephen; Moreira, Thais G; Freitas-Lopes, Maria Alice; Araújo, Alan M; Paul, Nicole E; Rezende, Rafael M; Menezes, Gustavo B.
Afiliação
  • David BA; Departamento de Morfologia, Center for Gastrointestinal Biology, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
  • Rubino S; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Moreira TG; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Freitas-Lopes MA; Departamento de Morfologia, Center for Gastrointestinal Biology, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
  • Araújo AM; Departamento de Morfologia, Center for Gastrointestinal Biology, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
  • Paul NE; Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
  • Rezende RM; Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Menezes GB; Departamento de Morfologia, Center for Gastrointestinal Biology, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Immunology ; 151(1): 56-70, 2017 05.
Article em En | MEDLINE | ID: mdl-28039862
ABSTRACT
The gastrointestinal immune system plays a pivotal role in the host relationship with food antigens, the homeostatic microbiome and enteric pathogens. Here, we describe how to collect and process liver and intestinal samples to efficiently isolate and analyse resident immune cells. Furthermore, we describe a step-by-step methodology showing how to high-dimensionally immunophenotype resident leucocytes using cytometry by time-of-flight, providing a well-characterized antibody platform that allows the identification of every leucocyte subset simultaneously. This protocol also includes instructions to purify and cultivate primary murine hepatocytes, a powerful tool to assess basic cell biology and toxicology assays. Gut and liver samples from the same mouse can be collected, processed and stained in less than 6 hr. This protocol enables the recovery of several populations of purified and viable immune cells from solid and fibrous organs, preventing unwanted loss of adherent cells during isolation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Imunofenotipagem / Mucosa Intestinal / Leucócitos / Fígado / Linfonodos Limite: Animals Idioma: En Revista: Immunology Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Imunofenotipagem / Mucosa Intestinal / Leucócitos / Fígado / Linfonodos Limite: Animals Idioma: En Revista: Immunology Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Brasil