Cargando…

NCR1 Expression Identifies Canine Natural Killer Cell Subsets with Phenotypic Similarity to Human Natural Killer Cells

Canines spontaneously develop many cancers similar to humans – including osteosarcoma, leukemia, and lymphoma – offering the opportunity to study immune therapies in a genetically heterogeneous and immunocompetent environment. However, a lack of antibodies recognizing canine NK cell markers has resu...

Descripción completa

Detalles Bibliográficos
Autores principales: Foltz, Jennifer A., Somanchi, Srinivas S., Yang, Yanwen, Aquino-Lopez, Arianexys, Bishop, Erin E., Lee, Dean A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120128/
https://www.ncbi.nlm.nih.gov/pubmed/27933061
http://dx.doi.org/10.3389/fimmu.2016.00521
_version_ 1782469179789541376
author Foltz, Jennifer A.
Somanchi, Srinivas S.
Yang, Yanwen
Aquino-Lopez, Arianexys
Bishop, Erin E.
Lee, Dean A.
author_facet Foltz, Jennifer A.
Somanchi, Srinivas S.
Yang, Yanwen
Aquino-Lopez, Arianexys
Bishop, Erin E.
Lee, Dean A.
author_sort Foltz, Jennifer A.
collection PubMed
description Canines spontaneously develop many cancers similar to humans – including osteosarcoma, leukemia, and lymphoma – offering the opportunity to study immune therapies in a genetically heterogeneous and immunocompetent environment. However, a lack of antibodies recognizing canine NK cell markers has resulted in suboptimal characterization and unknown purity of NK cell products, hindering the development of canine models of NK cell adoptive immunotherapy. To this end, we generated a novel antibody to canine NCR1 (NKp46), the putative species-wide marker of NK cells, enabling purification of NK cells for further characterization. We demonstrate that CD3(−)/NKp46(+) cells in healthy and osteosarcoma-bearing canines have phenotypic similarity to human CD3(−)/NKp46(+) NK cells, expressing mRNA for CD16 and the natural cytotoxicity receptors NKp30, NKp44, and NKp80. Functionally, we demonstrate with the calcein release assay that canine CD3(−)/NKp46(+) cells kill canine tumor cell lines without prior sensitization and secrete IFN-γ, TNF-α, IL-8, IL-10, and granulocyte-macrophage colony-stimulating factor as measured by Luminex. Similar to human NK cells, CD3(−)/NKp46(+) cells expand rapidly on feeder cells expressing 4-1BBL and membrane-bound IL-21 (median = 20,283-fold in 21 days). Furthermore, we identify a minor Null population (CD3(−)/CD21(−)/CD14(−)/NKp46(−)) with reduced cytotoxicity against osteosarcoma cells, but similar cytokine secretion as CD3(−)/NKp46(+) cells. Null cells in canines and humans have reduced expression of NKG2D, NKp44, and CD16 compared to NKp46(+) NK cells and can be induced to express NKp46 with further expansion on feeder cells. In conclusion, we have identified and characterized canine NK cells, including an NKp46(−) subset of canine and human NK cells, using a novel anti-canine NKp46 antibody, and report robust ex vivo expansion of canine NK cells sufficient for adoptive immunotherapy.
format Online
Article
Text
id pubmed-5120128
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-51201282016-12-08 NCR1 Expression Identifies Canine Natural Killer Cell Subsets with Phenotypic Similarity to Human Natural Killer Cells Foltz, Jennifer A. Somanchi, Srinivas S. Yang, Yanwen Aquino-Lopez, Arianexys Bishop, Erin E. Lee, Dean A. Front Immunol Immunology Canines spontaneously develop many cancers similar to humans – including osteosarcoma, leukemia, and lymphoma – offering the opportunity to study immune therapies in a genetically heterogeneous and immunocompetent environment. However, a lack of antibodies recognizing canine NK cell markers has resulted in suboptimal characterization and unknown purity of NK cell products, hindering the development of canine models of NK cell adoptive immunotherapy. To this end, we generated a novel antibody to canine NCR1 (NKp46), the putative species-wide marker of NK cells, enabling purification of NK cells for further characterization. We demonstrate that CD3(−)/NKp46(+) cells in healthy and osteosarcoma-bearing canines have phenotypic similarity to human CD3(−)/NKp46(+) NK cells, expressing mRNA for CD16 and the natural cytotoxicity receptors NKp30, NKp44, and NKp80. Functionally, we demonstrate with the calcein release assay that canine CD3(−)/NKp46(+) cells kill canine tumor cell lines without prior sensitization and secrete IFN-γ, TNF-α, IL-8, IL-10, and granulocyte-macrophage colony-stimulating factor as measured by Luminex. Similar to human NK cells, CD3(−)/NKp46(+) cells expand rapidly on feeder cells expressing 4-1BBL and membrane-bound IL-21 (median = 20,283-fold in 21 days). Furthermore, we identify a minor Null population (CD3(−)/CD21(−)/CD14(−)/NKp46(−)) with reduced cytotoxicity against osteosarcoma cells, but similar cytokine secretion as CD3(−)/NKp46(+) cells. Null cells in canines and humans have reduced expression of NKG2D, NKp44, and CD16 compared to NKp46(+) NK cells and can be induced to express NKp46 with further expansion on feeder cells. In conclusion, we have identified and characterized canine NK cells, including an NKp46(−) subset of canine and human NK cells, using a novel anti-canine NKp46 antibody, and report robust ex vivo expansion of canine NK cells sufficient for adoptive immunotherapy. Frontiers Media S.A. 2016-11-23 /pmc/articles/PMC5120128/ /pubmed/27933061 http://dx.doi.org/10.3389/fimmu.2016.00521 Text en Copyright © 2016 Foltz, Somanchi, Yang, Aquino-Lopez, Bishop and Lee. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Foltz, Jennifer A.
Somanchi, Srinivas S.
Yang, Yanwen
Aquino-Lopez, Arianexys
Bishop, Erin E.
Lee, Dean A.
NCR1 Expression Identifies Canine Natural Killer Cell Subsets with Phenotypic Similarity to Human Natural Killer Cells
title NCR1 Expression Identifies Canine Natural Killer Cell Subsets with Phenotypic Similarity to Human Natural Killer Cells
title_full NCR1 Expression Identifies Canine Natural Killer Cell Subsets with Phenotypic Similarity to Human Natural Killer Cells
title_fullStr NCR1 Expression Identifies Canine Natural Killer Cell Subsets with Phenotypic Similarity to Human Natural Killer Cells
title_full_unstemmed NCR1 Expression Identifies Canine Natural Killer Cell Subsets with Phenotypic Similarity to Human Natural Killer Cells
title_short NCR1 Expression Identifies Canine Natural Killer Cell Subsets with Phenotypic Similarity to Human Natural Killer Cells
title_sort ncr1 expression identifies canine natural killer cell subsets with phenotypic similarity to human natural killer cells
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120128/
https://www.ncbi.nlm.nih.gov/pubmed/27933061
http://dx.doi.org/10.3389/fimmu.2016.00521
work_keys_str_mv AT foltzjennifera ncr1expressionidentifiescaninenaturalkillercellsubsetswithphenotypicsimilaritytohumannaturalkillercells
AT somanchisrinivass ncr1expressionidentifiescaninenaturalkillercellsubsetswithphenotypicsimilaritytohumannaturalkillercells
AT yangyanwen ncr1expressionidentifiescaninenaturalkillercellsubsetswithphenotypicsimilaritytohumannaturalkillercells
AT aquinolopezarianexys ncr1expressionidentifiescaninenaturalkillercellsubsetswithphenotypicsimilaritytohumannaturalkillercells
AT bishoperine ncr1expressionidentifiescaninenaturalkillercellsubsetswithphenotypicsimilaritytohumannaturalkillercells
AT leedeana ncr1expressionidentifiescaninenaturalkillercellsubsetswithphenotypicsimilaritytohumannaturalkillercells