Evidence map›Paper›PMID 26995463›Full record

ReviewBiochimica et biophysica acta2016

Roles for lipid heterogeneity in immunoreceptor signaling.

David Holowka, Barbara Baird

Abstract readReview
In one paragraph

Review in Biochimica et biophysica acta, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. The plasma membrane as an adaptable fluid mosaic.Biochimica et biophysica acta. Biomembranes · 2023
    Review
  6. Article
  7. Review
  8. Surface densities prewet a near-critical membrane.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  9. Lipid-based and protein-based interactions synergize transmembrane signaling stimulated by antigen clustering of IgE receptors.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

David HolowkaDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853, USA. Electronic address: dah24@cornell.edu.
Barbara BairdDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853, USA.

Funding

STUCTURE-FUNCTION RELATIONSHIPS OF IMMUNORECEPTORSR01AI018306 · NIAID · CORNELL UNIVERSITY ITHACA · PI BAIRD, BARBARA A · 1985 to 2014
$5.3M
INTERACTIVE STRUCTURES AND DYNAMICS OF ANTIGEN RECEPTORSR01AI022449 · NIAID · CORNELL UNIVERSITY ITHACA · PI HOLOWKA, DAVID A · 1985 to 2014
$3.6M
High Resolution Characterization of Receptor Signaling and RegulationR01GM117552 · NIGMS · CORNELL UNIVERSITY · PI BAIRD, BARBARA A, HOLOWKA, DAVID A · 2016 to 2023
$3.2M
Cortical Aging, Estrogen and BehaviorR01AG022499 · NIA · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI JURASKA, JANICE M · 2005 to 2009
$601k
Howard Hughes Medical InstituteNIAID NIH HHS R01 AI018306NIAID NIH HHS R01 AI022449NIAID NIH HHS R01 AI022499NIA NIH HHS R01 AG022499NIGMS NIH HHS R01 GM117552
6 · The paper itself

Abstract

Immune receptors that specifically recognize foreign antigens to activate leukocytes in adaptive immune responses belong to a family of multichain cell surface proteins. All of these contain immunoreceptor tyrosine-based activation motifs in one or more subunits that initiate signaling cascades following stimulated tyrosine phosphorylation by Src-family kinases. As highlighted in this review, lipids participate in this initial activation step, as well as in more downstream signaling steps. We summarize evidence for cholesterol-dependent ordered lipids serving to regulate the store-operated Ca(2+) channel, Orai1, and we describe the sensitivity of Orai1 coupling to the ER Ca(2+) sensor, STIM1, to inhibition by polyunsaturated fatty acids. Phosphoinositides play key roles in regulating STIM1-Orai1 coupling, as well as in the stimulated Ca(2+) oscillations that are a consequence of IgE receptor signaling in mast cells. They also participate in the coupling between the plasma membrane and the actin cytoskeleton, which regulates immune receptor responses in T cells, B cells, and mast cells, both positively and negatively, depending on the cellular context. Recent studies show that other phospholipids with mostly saturated acylation also participate in coupling between receptors and the actin cytoskeleton. Lipid heterogeneity is a central feature of the intimate relationship between the plasma membrane and the actin cytoskeleton. The detailed nature of these interactions and how they are dynamically regulated to initiate and propagate receptor-mediated cell signaling are challenging questions for further investigation. This article is part of a Special Issue entitled: The cellular lipid landscape edited by Tim P. Levine and Anant K. Menon.

Indexed as

AnimalsCalcium SignalingCell MembraneCytoskeletonHumansLipidsMembrane ProteinsPhospholipidsPhosphorylationReceptors, ImmunologicSignal TransductionLipidsMembrane ProteinsPhospholipidsReceptors, ImmunologicActin cytoskeletonCalcium mobilizationCritical fluctuationsIgE receptorsLiquid ordered lipidsPhosphoinositides

Identifiers

PMID26995463
PMCPMC5319924

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.