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Tissue-Specific Molecular Markers and Heterogeneity in Type 2 Innate Lymphoid Cells.
Olguín-Martínez, Enrique; Ruiz-Medina, Blanca E; Licona-Limón, Paula.
Affiliation
  • Olguín-Martínez E; Departamento de Biología Celular y del Desarrollo, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, México City, Mexico.
  • Ruiz-Medina BE; Departamento de Biología Celular y del Desarrollo, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, México City, Mexico.
  • Licona-Limón P; Departamento de Biología Celular y del Desarrollo, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, México City, Mexico.
Front Immunol ; 12: 757967, 2021.
Article in En | MEDLINE | ID: mdl-34759931
Innate lymphoid cells (ILCs) are the most recently described group of lymphoid subpopulations. These tissue-resident cells display a heterogeneity resembling that observed on different groups of T cells, hence their categorization as cytotoxic NK cells and helper ILCs type 1, 2 and 3. Each one of these groups is highly diverse and expresses different markers in a context-dependent manner. Type 2 innate lymphoid cells (ILC2s) are activated in response to helminth parasites and regulate the immune response. They are involved in the etiology of diseases associated with allergic responses as well as in the maintenance of tissue homeostasis. Markers associated with their identification differ depending on the tissue and model used, making the study and understanding of these cells a cumbersome task. This review compiles evidence for the heterogeneity of ILC2s as well as discussion and analyses of molecular markers associated with their identity, function, tissue-dependent expression, and how these markers contribute to the interaction of ILC2s with specific microenvironments to maintain homeostasis or respond to pathogenic challenges.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antigens, Differentiation / Lymphocyte Subsets Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: Front Immunol Year: 2021 Document type: Article Affiliation country: México Country of publication: Suiza

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antigens, Differentiation / Lymphocyte Subsets Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: Front Immunol Year: 2021 Document type: Article Affiliation country: México Country of publication: Suiza