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A forward genetic screen reveals novel independent regulators of ULBP1, an activating ligand for natural killer cells

Recognition and elimination of tumor cells by the immune system is crucial for limiting tumor growth. Natural killer (NK) cells become activated when the receptor NKG2D is engaged by ligands that are frequently upregulated in primary tumors and on cancer cell lines. However, the molecular mechanisms...

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Autores principales: Gowen, Benjamin G, Chim, Bryan, Marceau, Caleb D, Greene, Trever T, Burr, Patrick, Gonzalez, Jeanmarie R, Hesser, Charles R, Dietzen, Peter A, Russell, Teal, Iannello, Alexandre, Coscoy, Laurent, Sentman, Charles L, Carette, Jan E, Muljo, Stefan A, Raulet, David H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4629278/
https://www.ncbi.nlm.nih.gov/pubmed/26565589
http://dx.doi.org/10.7554/eLife.08474
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author Gowen, Benjamin G
Chim, Bryan
Marceau, Caleb D
Greene, Trever T
Burr, Patrick
Gonzalez, Jeanmarie R
Hesser, Charles R
Dietzen, Peter A
Russell, Teal
Iannello, Alexandre
Coscoy, Laurent
Sentman, Charles L
Carette, Jan E
Muljo, Stefan A
Raulet, David H
author_facet Gowen, Benjamin G
Chim, Bryan
Marceau, Caleb D
Greene, Trever T
Burr, Patrick
Gonzalez, Jeanmarie R
Hesser, Charles R
Dietzen, Peter A
Russell, Teal
Iannello, Alexandre
Coscoy, Laurent
Sentman, Charles L
Carette, Jan E
Muljo, Stefan A
Raulet, David H
author_sort Gowen, Benjamin G
collection PubMed
description Recognition and elimination of tumor cells by the immune system is crucial for limiting tumor growth. Natural killer (NK) cells become activated when the receptor NKG2D is engaged by ligands that are frequently upregulated in primary tumors and on cancer cell lines. However, the molecular mechanisms driving NKG2D ligand expression on tumor cells are not well defined. Using a forward genetic screen in a tumor-derived human cell line, we identified several novel factors supporting expression of the NKG2D ligand ULBP1. Our results show stepwise contributions of independent pathways working at multiple stages of ULBP1 biogenesis. Deeper investigation of selected hits from the screen showed that the transcription factor ATF4 drives ULBP1 gene expression in cancer cell lines, while the RNA-binding protein RBM4 supports ULBP1 expression by suppressing a novel alternatively spliced isoform of ULBP1 mRNA. These findings offer insight into the stress pathways that alert the immune system to danger. DOI: http://dx.doi.org/10.7554/eLife.08474.001
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spelling pubmed-46292782015-11-14 A forward genetic screen reveals novel independent regulators of ULBP1, an activating ligand for natural killer cells Gowen, Benjamin G Chim, Bryan Marceau, Caleb D Greene, Trever T Burr, Patrick Gonzalez, Jeanmarie R Hesser, Charles R Dietzen, Peter A Russell, Teal Iannello, Alexandre Coscoy, Laurent Sentman, Charles L Carette, Jan E Muljo, Stefan A Raulet, David H eLife Immunology Recognition and elimination of tumor cells by the immune system is crucial for limiting tumor growth. Natural killer (NK) cells become activated when the receptor NKG2D is engaged by ligands that are frequently upregulated in primary tumors and on cancer cell lines. However, the molecular mechanisms driving NKG2D ligand expression on tumor cells are not well defined. Using a forward genetic screen in a tumor-derived human cell line, we identified several novel factors supporting expression of the NKG2D ligand ULBP1. Our results show stepwise contributions of independent pathways working at multiple stages of ULBP1 biogenesis. Deeper investigation of selected hits from the screen showed that the transcription factor ATF4 drives ULBP1 gene expression in cancer cell lines, while the RNA-binding protein RBM4 supports ULBP1 expression by suppressing a novel alternatively spliced isoform of ULBP1 mRNA. These findings offer insight into the stress pathways that alert the immune system to danger. DOI: http://dx.doi.org/10.7554/eLife.08474.001 eLife Sciences Publications, Ltd 2015-11-13 /pmc/articles/PMC4629278/ /pubmed/26565589 http://dx.doi.org/10.7554/eLife.08474 Text en http://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (http://creativecommons.org/publicdomain/zero/1.0/) .
spellingShingle Immunology
Gowen, Benjamin G
Chim, Bryan
Marceau, Caleb D
Greene, Trever T
Burr, Patrick
Gonzalez, Jeanmarie R
Hesser, Charles R
Dietzen, Peter A
Russell, Teal
Iannello, Alexandre
Coscoy, Laurent
Sentman, Charles L
Carette, Jan E
Muljo, Stefan A
Raulet, David H
A forward genetic screen reveals novel independent regulators of ULBP1, an activating ligand for natural killer cells
title A forward genetic screen reveals novel independent regulators of ULBP1, an activating ligand for natural killer cells
title_full A forward genetic screen reveals novel independent regulators of ULBP1, an activating ligand for natural killer cells
title_fullStr A forward genetic screen reveals novel independent regulators of ULBP1, an activating ligand for natural killer cells
title_full_unstemmed A forward genetic screen reveals novel independent regulators of ULBP1, an activating ligand for natural killer cells
title_short A forward genetic screen reveals novel independent regulators of ULBP1, an activating ligand for natural killer cells
title_sort forward genetic screen reveals novel independent regulators of ulbp1, an activating ligand for natural killer cells
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4629278/
https://www.ncbi.nlm.nih.gov/pubmed/26565589
http://dx.doi.org/10.7554/eLife.08474
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