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MMTV Env encodes an ITAM responsible for transformation of mammary epithelial cells in three-dimensional culture

Expression of immunoreceptor tyrosine-based activation motif (ITAM)-containing signaling proteins is normally restricted to hematopoietic tissues. The basal activity of ITAM-containing proteins is mediated through negative regulation by coreceptors restricted to hematopoietic tissues. We have identi...

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Autores principales: Katz, Elad, Lareef, Mohamed H., Rassa, John C., Grande, Shannon M., King, Leslie B., Russo, Jose, Ross, Susan R., Monroe, John G.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213037/
https://www.ncbi.nlm.nih.gov/pubmed/15684322
http://dx.doi.org/10.1084/jem.20041471
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author Katz, Elad
Lareef, Mohamed H.
Rassa, John C.
Grande, Shannon M.
King, Leslie B.
Russo, Jose
Ross, Susan R.
Monroe, John G.
author_facet Katz, Elad
Lareef, Mohamed H.
Rassa, John C.
Grande, Shannon M.
King, Leslie B.
Russo, Jose
Ross, Susan R.
Monroe, John G.
author_sort Katz, Elad
collection PubMed
description Expression of immunoreceptor tyrosine-based activation motif (ITAM)-containing signaling proteins is normally restricted to hematopoietic tissues. The basal activity of ITAM-containing proteins is mediated through negative regulation by coreceptors restricted to hematopoietic tissues. We have identified an ITAM signaling domain encoded within the env gene of murine mammary tumor virus (MMTV). Three-dimensional structures derived in vitro from murine cells stably transfected with MMTV env display a depolarized morphology in comparison with control mammary epithelial cells. This effect is abolished by Y>F substitution within the Env ITAM, as well as inhibitors of Syk and Src protein tyrosine kinases. Env-expressing cells bear hallmarks of cell transformation such as sensitivity to apoptosis induced by tumor necrosis factor (TNF)–related apoptosis-inducing ligand (TRAIL) or TNFα, as well as down-regulation of E-cadherin and Keratin-18. Human normal mammary epithelial cells expressing MMTV Env also develop transformed phenotype, as typified by growth in soft agar and Matrigel invasion. These disruptions are abrogated by Y>F substitutions. We conclude that ITAM-dependent signals are generated through MMTV Env and trigger early hallmarks of transformation of mouse and human mammary epithelial cells. Therefore, these data suggest a heretofore unappreciated potential mechanism for the initiation of breast cancer and identify MMTV Env and ITAM-containing proteins in human breast tumors as probable oncoproteins.
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spelling pubmed-22130372008-03-11 MMTV Env encodes an ITAM responsible for transformation of mammary epithelial cells in three-dimensional culture Katz, Elad Lareef, Mohamed H. Rassa, John C. Grande, Shannon M. King, Leslie B. Russo, Jose Ross, Susan R. Monroe, John G. J Exp Med Article Expression of immunoreceptor tyrosine-based activation motif (ITAM)-containing signaling proteins is normally restricted to hematopoietic tissues. The basal activity of ITAM-containing proteins is mediated through negative regulation by coreceptors restricted to hematopoietic tissues. We have identified an ITAM signaling domain encoded within the env gene of murine mammary tumor virus (MMTV). Three-dimensional structures derived in vitro from murine cells stably transfected with MMTV env display a depolarized morphology in comparison with control mammary epithelial cells. This effect is abolished by Y>F substitution within the Env ITAM, as well as inhibitors of Syk and Src protein tyrosine kinases. Env-expressing cells bear hallmarks of cell transformation such as sensitivity to apoptosis induced by tumor necrosis factor (TNF)–related apoptosis-inducing ligand (TRAIL) or TNFα, as well as down-regulation of E-cadherin and Keratin-18. Human normal mammary epithelial cells expressing MMTV Env also develop transformed phenotype, as typified by growth in soft agar and Matrigel invasion. These disruptions are abrogated by Y>F substitutions. We conclude that ITAM-dependent signals are generated through MMTV Env and trigger early hallmarks of transformation of mouse and human mammary epithelial cells. Therefore, these data suggest a heretofore unappreciated potential mechanism for the initiation of breast cancer and identify MMTV Env and ITAM-containing proteins in human breast tumors as probable oncoproteins. The Rockefeller University Press 2005-02-07 /pmc/articles/PMC2213037/ /pubmed/15684322 http://dx.doi.org/10.1084/jem.20041471 Text en Copyright © 2005, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Katz, Elad
Lareef, Mohamed H.
Rassa, John C.
Grande, Shannon M.
King, Leslie B.
Russo, Jose
Ross, Susan R.
Monroe, John G.
MMTV Env encodes an ITAM responsible for transformation of mammary epithelial cells in three-dimensional culture
title MMTV Env encodes an ITAM responsible for transformation of mammary epithelial cells in three-dimensional culture
title_full MMTV Env encodes an ITAM responsible for transformation of mammary epithelial cells in three-dimensional culture
title_fullStr MMTV Env encodes an ITAM responsible for transformation of mammary epithelial cells in three-dimensional culture
title_full_unstemmed MMTV Env encodes an ITAM responsible for transformation of mammary epithelial cells in three-dimensional culture
title_short MMTV Env encodes an ITAM responsible for transformation of mammary epithelial cells in three-dimensional culture
title_sort mmtv env encodes an itam responsible for transformation of mammary epithelial cells in three-dimensional culture
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213037/
https://www.ncbi.nlm.nih.gov/pubmed/15684322
http://dx.doi.org/10.1084/jem.20041471
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