Literature DB >> 28961325

A Brake for B Cell Proliferation: Appropriate responses to metabolic stress are crucial to maintain B cell viability and prevent malignant outgrowth.

Julia Jellusova1,2,3, Robert C Rickert4.   

Abstract

B cell activation is accompanied by metabolic adaptations to meet the increased energetic demands of proliferation. The metabolic composition of the microenvironment is known to change during a germinal center response, in inflamed tissue and to vary significantly between different organs. To sustain cellular homeostasis B cells need to be able to dynamically adapt to changes in their environment. An inability to take up and process available nutrients can result in impaired B cell growth and a diminished humoral immune response. Furthermore, the metabolic microenvironment can affect B cell signaling and provide a means to avoid aberrant proliferation or modulate B cell function. Thus, a better understanding of the intricate interplay between cell signaling and metabolism could provide novel insight into how B cell function is regulated and have implications for the development of vaccines or treatment of autoimmune disorders and B cell derived malignancies.
© 2017 WILEY Periodicals, Inc.

Entities:  

Keywords:  GSK3; germinal center; hypoxia; lymphocyte; metabolism; senescence

Mesh:

Year:  2017        PMID: 28961325     DOI: 10.1002/bies.201700079

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  9 in total

1.  AMPKα1 in B Cells Dampens Primary Antibody Responses yet Promotes Mitochondrial Homeostasis and Persistence of B Cell Memory.

Authors:  Shawna K Brookens; Sung Hoon Cho; Paulo J Basso; Mark R Boothby
Journal:  J Immunol       Date:  2020-11-04       Impact factor: 5.422

2.  IP3R-mediated Ca2+ signaling controls B cell proliferation through metabolic reprogramming.

Authors:  Huayuan Tang; Yali Li; Shijia Wang; Jing Ji; Xiangbin Zhu; Yutong Bao; Can Huang; Ye Luo; Lei Huang; Yan Gao; Chaoliang Wei; Jie Liu; Xi Fang; Lu Sun; Kunfu Ouyang
Journal:  iScience       Date:  2022-04-06

Review 3.  Immunometabolism of Phagocytes During Mycobacterium tuberculosis Infection.

Authors:  Ranjeet Kumar; Pooja Singh; Afsal Kolloli; Lanbo Shi; Yuri Bushkin; Sanjay Tyagi; Selvakumar Subbian
Journal:  Front Mol Biosci       Date:  2019-10-14

4.  Systematic Enzyme Mapping of Cellular Metabolism by Phasor-Analyzed Label-Free NAD(P)H Fluorescence Lifetime Imaging.

Authors:  Ruth Leben; Markus Köhler; Helena Radbruch; Anja E Hauser; Raluca A Niesner
Journal:  Int J Mol Sci       Date:  2019-11-07       Impact factor: 5.923

Review 5.  The Wanderings of Gut-Derived IgA Plasma Cells: Impact on Systemic Immune Responses.

Authors:  Selina J Keppler; Marie Christine Goess; Julia M Heinze
Journal:  Front Immunol       Date:  2021-04-15       Impact factor: 7.561

6.  AMPK Metabolism in the B Lineage Modulates Humoral Responses.

Authors:  Shawna K Brookens; Mark R Boothby
Journal:  Immunometabolism       Date:  2021-02-12

7.  Hepatitis B virus particles activate B cells through the TLR2-MyD88-mTOR axis.

Authors:  Qian Li; Jun Wang; Heba Islam; Carsten Kirschning; Hongzhou Lu; Daniel Hoffmann; Ulf Dittmer; Mengji Lu
Journal:  Cell Death Dis       Date:  2021-01-04       Impact factor: 8.469

Review 8.  Epigenetic, Metabolic, and Immune Crosstalk in Germinal-Center-Derived B-Cell Lymphomas: Unveiling New Vulnerabilities for Rational Combination Therapies.

Authors:  Inna Serganova; Sanjukta Chakraborty; Samuel Yamshon; Yusuke Isshiki; Ryan Bucktrout; Ari Melnick; Wendy Béguelin; Roberta Zappasodi
Journal:  Front Cell Dev Biol       Date:  2022-01-07

9.  Initial B Cell Activation Induces Metabolic Reprogramming and Mitochondrial Remodeling.

Authors:  Lynnea R Waters; Fasih M Ahsan; Dane M Wolf; Orian Shirihai; Michael A Teitell
Journal:  iScience       Date:  2018-07-10
  9 in total

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