Evidence map›Paper›PMID 19290935›Full record

ReviewImmunological reviews2009

CD45, CD148, and Lyp/Pep: critical phosphatases regulating Src family kinase signaling networks in immune cells.

Michelle L Hermiston, Julie Zikherman, Jing W Zhu

Erratum issuedOpen access · greenAbstract readReview
In one paragraph

Review in Immunological reviews, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 93 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed, 1 pooled it
7.0field-weighted citation impact, top 2% of its field
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

93 citing papers in PubMed, 1 synthesis or guideline pooled it, 166 citations in OpenAlex.

  1. Pooled it
  2. Review
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  12. Propulsive cell entry diverts pathogens from immune degradation by remodeling the phagocytic synapse.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
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  16. Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2022
    Article
  17. Article
  18. Review
  19. Review
  20. Article

33 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Michelle L HermistonDepartment of Pediatrics, University of California, San Francisco, CA 94143, USA. HermistonM@peds.ucsf.edu
Julie Zikherman
Jing W Zhu
University of California, San Francisco · US

Funding

Src tyrosine kinases and autoimmunity.P01AI035297 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ANDERSON, MARK S · 1993 to 2010
$16.5M
Role of CD45 in Hematopoiesis and LymphomagenesisK08CA098418 · NCI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI HERMISTON, MICHELLE L · 2003 to 2005
$382k
NCI NIH HHS K08 CA098418NIAID NIH HHS P01 AI035297NIAID NIH HHS P01 AI355297
6 · The paper itself

Abstract

Reciprocal regulation of tyrosine phosphorylation by protein tyrosine kinases (PTKs) and protein tyrosine phosphatases (PTPs) is central to normal immune cell function. Disruption of the equilibrium between PTK and PTP activity can result in immunodeficiency, autoimmunity, or malignancy. Src family kinases (SFKs) play a central role in both immune cell function and disease due to their proximal position in numerous signal transduction cascades including those emanating from integrin, T and B-cell antigen receptors, Fc, growth factor, and cytokine receptors. Given that tight regulation of SFKs activity is critical for appropriate responses to stimulation of these various signaling pathways, it is perhaps not surprising that multiple PTPs are involved in their regulation. Here, we focus on the role of three phosphatases, CD45, CD148, and LYP/PEP, which are critical regulators of SFKs in hematopoietic cells. We review our current understanding of their structures, expression, functions in different hematopoietic cell subsets, regulation, and putative roles in disease. Finally, we discuss remaining questions that must be addressed if we are to have a clearer understanding of the coordinated regulation of tyrosine phosphorylation and signaling networks in hematopoietic cells and how they could potentially be manipulated therapeutically in disease.

Indexed as

Signal TransductionAnimalsBlood CellsHumansLeukocyte Common AntigensProtein Tyrosine Phosphatase, Non-Receptor Type 12Receptor-Like Protein Tyrosine Phosphatases, Class 3Leukocyte Common AntigensProtein Tyrosine Phosphatase, Non-Receptor Type 12PTPRJ protein, humanReceptor-Like Protein Tyrosine Phosphatases, Class 3

Identifiers

PMID19290935
PMCPMC2739744
OpenAlexW2114876320

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.