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Aging-associated inflammation promotes selection for adaptive oncogenic events in B cell progenitors
Curtis J. Henry, … , Charles A. Dinarello, James DeGregori
Curtis J. Henry, … , Charles A. Dinarello, James DeGregori
Published November 9, 2015
Citation Information: J Clin Invest. 2015;125(12):4666-4680. https://doi.org/10.1172/JCI83024.
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Research Article Aging Article has an altmetric score of 18

Aging-associated inflammation promotes selection for adaptive oncogenic events in B cell progenitors

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Abstract

The incidence of cancer is higher in the elderly; however, many of the underlying mechanisms for this association remain unexplored. Here, we have shown that B cell progenitors in old mice exhibit marked signaling, gene expression, and metabolic defects. Moreover, B cell progenitors that developed from hematopoietic stem cells (HSCs) transferred from young mice into aged animals exhibited similar fitness defects. We further demonstrated that ectopic expression of the oncogenes BCR-ABL, NRASV12, or Myc restored B cell progenitor fitness, leading to selection for oncogenically initiated cells and leukemogenesis specifically in the context of an aged hematopoietic system. Aging was associated with increased inflammation in the BM microenvironment, and induction of inflammation in young mice phenocopied aging-associated B lymphopoiesis. Conversely, a reduction of inflammation in aged mice via transgenic expression of α-1-antitrypsin or IL-37 preserved the function of B cell progenitors and prevented NRASV12-mediated oncogenesis. We conclude that chronic inflammatory microenvironments in old age lead to reductions in the fitness of B cell progenitor populations. This reduced progenitor pool fitness engenders selection for cells harboring oncogenic mutations, in part due to their ability to correct aging-associated functional defects. Thus, modulation of inflammation — a common feature of aging — has the potential to limit aging-associated oncogenesis.

Authors

Curtis J. Henry, Matias Casás-Selves, Jihye Kim, Vadym Zaberezhnyy, Leila Aghili, Ashley E. Daniel, Linda Jimenez, Tania Azam, Eoin N. McNamee, Eric T. Clambey, Jelena Klawitter, Natalie J. Serkova, Aik Choon Tan, Charles A. Dinarello, James DeGregori

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Figure 2

Oncogenic mutations correct aging-associated functional defects in B progenitors, leading to increased leukemogenesis.

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Oncogenic mutations correct aging-associated functional defects in B pro...
(A) Ba/F3 cells expressing vector (V) or oncogenes (BCR-ABL, NRASV12, Myc) were grown in various concentrations of IL-3 for 24 hours, and STAT5 activation in these cells was determined by flow cytometry. (B) Ba/F3 cells were grown overnight in media containing or lacking IL-3, and expression levels of Myc and Hprt in these cells were determined by qPCR. Values in A and B represent the mean ± SEM of 3 independent experiments (9 total samples). (C–F) c-KIT+ BM cells were isolated from young (2-month-old) or old (24-month-old) mice, retrovirally transduced to express vector or oncogenic BCR-ABL, NRASV12,, or Myc (each with coexpressed GFP), and transplanted into sublethally irradiated young BALB/c mice. Three weeks after transplantation, mice were sacrificed, and STAT5 activity (C) and mRNA levels of Hprt, Myc, and Ebf (D–F) were determined in vector-expressing or oncogene-expressing pro–B cell progenitors. Values in C–F represent the mean ± SEM for more than 5 mice per group. (G and H) Young mice were lethally irradiated and transplanted with either 2 × 106 young or old whole BM cells. Four days later, mice reconstituted with young or old BM cells were transplanted, respectively, with young or old c-KIT+ cells expressing oncogenic NRASV12 or Myc. Leukemia-free survival is plotted using Kaplan-Meier graphs. Most mice developed B220+CD43+ pro–B cell–like acute lymphoblastic leukemia (ALL) (87% and 80% for NRAS- and Myc-driven leukemias, respectively, on the old backgrounds). (I) Young or old mice were treated with busulfan and transplanted with young or old c-KIT+ cells expressing oncogenic NRASV12. Leukemia-free survival is plotted using Kaplan-Meier graphs. Values in G and H represent the mean ± SEM of 2 independent experiments, with more than 15 mice per group in total, and values in I represent 5 mice per treatment group. (A–F) **P < 0.01 and #P < 0.001, by Student’s t test . In C–F, oncogene-bearing samples were compared with vector-expressing controls (old to old). (G–I) **P < 0.01 and #P < 0.001, by Cox proportional hazards test. BMT, BM transplantation.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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