Cited by 206Redox biology and oxidative stressProtein Kinase Regulation and GTPase SignalingReceptor Mechanisms and Signaling

The strength of receptor signaling is centrally controlled through a cooperative loop between Ca2+ and an oxidant signal

Open access
Singh, Dinesh Kumar, Kumar, Dhiraj, Siddiqui, Zaved, Basu, Sandip Kumar, Kumar, Vikas, Rao, Kanury V.S.·2005·Cell

Abstract

Activation of cell-surface receptors stimulates generation of intracellular signals that, in turn, direct the cellular response. However, mechanisms that ensure combinatorial control of these signaling events are not well understood. We show here that the Ca2+ and reactive oxygen intermediates generated upon BCR activation rapidly engage in a cooperative interaction that acts in a feedback manner to amplify the early signal generated. This cooperativity acts by regulating the concentration of the oxidant produced. The latter exerts its influence through a pulsed inactivation of receptor-coupled phosphatases, where the amplitude of this pulse is determined by oxidant concentration. The extent of phosphatase inhibition, in turn, dictates what proportion of receptor-proximal kinases are activated and, as a result, the net strength of the initial signal. It is the strength of this initial signal that finally determines the eventual duration of BCR signaling and the rate of its transmission through downstream pathways.

Integrity signals

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Crossref · 10.1016/j.cell.2005.02.036

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  • BCR ligation causes calcium release into the cytoplasm, promoting ROS production and inactivation of receptor-coupled phosphatases, which allows downstream signaling pathways to activate.

    “Specifically, BCR ligation stimulates calcium release into the cytoplasm that promotes ROS production and inactivation of receptor-coupled phosphates, allowing for activation of downstream signaling pathways.”

    From Mitochondria in the Regulation of Innate and Adaptive Immunity (2015) · cites this paper as Singh et al., 2005

  • B cell receptor (BCR) activation is regulated by ROS.

    “Along with these changes in metabolism, B cell receptor (BCR) activation is regulated by ROS (Capasso et al., 2010; Singh et al., 2005).”

    From Mitochondria in the Regulation of Innate and Adaptive Immunity (2015) · cites this paper as Singh et al., 2005

  • The size of the ROS pulse determines how long BCR signaling lasts and how strongly downstream pathways are activated.

    “Depending on the magnitude of the ROS pulse, there is increased duration of BCR signaling and enhanced activation of downstream signaling pathways (Singh et al., 2005).”

    From Mitochondria in the Regulation of Innate and Adaptive Immunity (2015) · cites this paper as Singh et al., 2005

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References 39 · Cited by 206

Authors
Singh, D. K., Kumar, D., Siddiqui, Z., Basu, S. K., Kumar, V., & Rao, K. V. S.
Affiliations
International Centre for Genetic Engineering and Biotechnology (IN)
Corresponding author
Rao, Kanury V.S.
Venue
Cell
Publisher
Elsevier BV
Published
2005-04
Volume
121
Issue
2
Pages
281-293
ISSN
0092-8674 (ISSN-L)
OpenAlex
W1968332969
Cited by
206
References
39
Citations by year
2026: 1 · 2025: 4 · 2024: 4 · 2023: 1 · 2022: 2 · 2021: 5 · 2020: 4 · 2019: 6 · 2018: 8 · 2017: 11 · 2016: 10 · 2015: 9 · 2014: 9 · 2013: 10 · 2012: 12
FWCI
7.93
Type
journal article
Language
en
Open access
Locations
  • Cell (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
Keywords
B cell receptor signaling, calcium signaling, reactive oxygen species, signal amplification, feedback loops, kinase activation, signal duration, signal transduction
MeSH terms
Dual Oxidases, Calcium, Flavoproteins, Humans, Phosphoric Monoester Hydrolases, Phosphorylation, Receptors, Antigen, B-Cell, Transfection, Signal Transduction, Reactive Oxygen Species, Protein Structure, Tertiary, NADPH Oxidases, Feedback, Physiological

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