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Therapeutic targeting of NOTCH signaling ameliorates immune-mediated bone marrow failure of aplastic anemia

Severe aplastic anemia (AA) is a bone marrow (BM) failure (BMF) disease frequently caused by aberrant immune destruction of blood progenitors. Although a Th1-mediated pathology is well described for AA, molecular mechanisms driving disease progression remain ill defined. The NOTCH signaling pathway...

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Autores principales: Roderick, Justine E., Gonzalez-Perez, Gabriela, Kuksin, Christina Arieta, Dongre, Anushka, Roberts, Emily R., Srinivasan, Janani, Andrzejewski, Chester, Fauq, Abdul H., Golde, Todd E., Miele, Lucio, Minter, Lisa M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3698520/
https://www.ncbi.nlm.nih.gov/pubmed/23733784
http://dx.doi.org/10.1084/jem.20112615
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author Roderick, Justine E.
Gonzalez-Perez, Gabriela
Kuksin, Christina Arieta
Dongre, Anushka
Roberts, Emily R.
Srinivasan, Janani
Andrzejewski, Chester
Fauq, Abdul H.
Golde, Todd E.
Miele, Lucio
Minter, Lisa M.
author_facet Roderick, Justine E.
Gonzalez-Perez, Gabriela
Kuksin, Christina Arieta
Dongre, Anushka
Roberts, Emily R.
Srinivasan, Janani
Andrzejewski, Chester
Fauq, Abdul H.
Golde, Todd E.
Miele, Lucio
Minter, Lisa M.
author_sort Roderick, Justine E.
collection PubMed
description Severe aplastic anemia (AA) is a bone marrow (BM) failure (BMF) disease frequently caused by aberrant immune destruction of blood progenitors. Although a Th1-mediated pathology is well described for AA, molecular mechanisms driving disease progression remain ill defined. The NOTCH signaling pathway mediates Th1 cell differentiation in the presence of polarizing cytokines, an action requiring enzymatic processing of NOTCH receptors by γ-secretase. Using a mouse model of AA, we demonstrate that expression of both intracellular NOTCH1(IC) and T-BET, a key transcription factor regulating Th1 cell differentiation, was increased in spleen and BM-infiltrating T cells during active disease. Conditionally deleting Notch1 or administering γ-secretase inhibitors (GSIs) in vivo attenuated disease and rescued mice from lethal BMF. In peripheral T cells from patients with untreated AA, NOTCH1(IC) was significantly elevated and bound to the TBX21 promoter, showing NOTCH1 directly regulates the gene encoding T-BET. Treating patient cells with GSIs in vitro lowered NOTCH1(IC) levels, decreased NOTCH1 detectable at the TBX21 promoter, and decreased T-BET expression, indicating that NOTCH1 signaling is responsive to GSIs during active disease. Collectively, these results identify NOTCH signaling as a primary driver of Th1-mediated pathogenesis in AA and may represent a novel target for therapeutic intervention.
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spelling pubmed-36985202014-01-01 Therapeutic targeting of NOTCH signaling ameliorates immune-mediated bone marrow failure of aplastic anemia Roderick, Justine E. Gonzalez-Perez, Gabriela Kuksin, Christina Arieta Dongre, Anushka Roberts, Emily R. Srinivasan, Janani Andrzejewski, Chester Fauq, Abdul H. Golde, Todd E. Miele, Lucio Minter, Lisa M. J Exp Med Article Severe aplastic anemia (AA) is a bone marrow (BM) failure (BMF) disease frequently caused by aberrant immune destruction of blood progenitors. Although a Th1-mediated pathology is well described for AA, molecular mechanisms driving disease progression remain ill defined. The NOTCH signaling pathway mediates Th1 cell differentiation in the presence of polarizing cytokines, an action requiring enzymatic processing of NOTCH receptors by γ-secretase. Using a mouse model of AA, we demonstrate that expression of both intracellular NOTCH1(IC) and T-BET, a key transcription factor regulating Th1 cell differentiation, was increased in spleen and BM-infiltrating T cells during active disease. Conditionally deleting Notch1 or administering γ-secretase inhibitors (GSIs) in vivo attenuated disease and rescued mice from lethal BMF. In peripheral T cells from patients with untreated AA, NOTCH1(IC) was significantly elevated and bound to the TBX21 promoter, showing NOTCH1 directly regulates the gene encoding T-BET. Treating patient cells with GSIs in vitro lowered NOTCH1(IC) levels, decreased NOTCH1 detectable at the TBX21 promoter, and decreased T-BET expression, indicating that NOTCH1 signaling is responsive to GSIs during active disease. Collectively, these results identify NOTCH signaling as a primary driver of Th1-mediated pathogenesis in AA and may represent a novel target for therapeutic intervention. The Rockefeller University Press 2013-07-01 /pmc/articles/PMC3698520/ /pubmed/23733784 http://dx.doi.org/10.1084/jem.20112615 Text en © 2013 Roderick et al. 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Article
Roderick, Justine E.
Gonzalez-Perez, Gabriela
Kuksin, Christina Arieta
Dongre, Anushka
Roberts, Emily R.
Srinivasan, Janani
Andrzejewski, Chester
Fauq, Abdul H.
Golde, Todd E.
Miele, Lucio
Minter, Lisa M.
Therapeutic targeting of NOTCH signaling ameliorates immune-mediated bone marrow failure of aplastic anemia
title Therapeutic targeting of NOTCH signaling ameliorates immune-mediated bone marrow failure of aplastic anemia
title_full Therapeutic targeting of NOTCH signaling ameliorates immune-mediated bone marrow failure of aplastic anemia
title_fullStr Therapeutic targeting of NOTCH signaling ameliorates immune-mediated bone marrow failure of aplastic anemia
title_full_unstemmed Therapeutic targeting of NOTCH signaling ameliorates immune-mediated bone marrow failure of aplastic anemia
title_short Therapeutic targeting of NOTCH signaling ameliorates immune-mediated bone marrow failure of aplastic anemia
title_sort therapeutic targeting of notch signaling ameliorates immune-mediated bone marrow failure of aplastic anemia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3698520/
https://www.ncbi.nlm.nih.gov/pubmed/23733784
http://dx.doi.org/10.1084/jem.20112615
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