Evidence map›Paper›PMID 22534490›Full record

ArticleCirculation research2012

A novel role for type 1 angiotensin receptors on T lymphocytes to limit target organ damage in hypertension.

Jian-dong Zhang, Mehul B Patel, Young-Soo Song, Robert Griffiths, James Burchette, Phillip Ruiz, Matthew A Sparks, Ming Yan, David N Howell, Jose A Gomez and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Circulation research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 1 pooled it
8.0field-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

78 citing papers in PubMed, 1 synthesis or guideline pooled it, 119 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Immune and inflammatory mechanisms in hypertension.Nature reviews. Cardiology · 2024
    Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Angiotensin II enhances bacterial clearance via myeloid signaling in a murine sepsis model.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Role of T cells in ischemic acute kidney injury and repair.The Korean journal of internal medicine · 2022
    Review
  18. O-Linked β-Frontiers in immunology · 2022
    Review
  19. Review
  20. CCL5 Suppresses Klotho ExpressionFrontiers in physiology · 2022
    Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 1 institution in 1 country.

Jian-dong ZhangDivision of Nephrology, Departments of Medicine, Duke University Medical Center and Durham VA Medical Center, Durham, NC 27710, USA.
Mehul B Patel
Young-Soo Song
Robert Griffiths
James Burchette
Phillip Ruiz
Matthew A Sparks
Ming Yan
David N Howell
Jose A Gomez
Robert F Spurney
Thomas M Coffman
Steven D Crowley
University of Miami · US

Funding

Role of Th1 Immune Responses in the Pathogenesis of Hypertensive Kidney InjuryR01DK087893 · NIDDK · DUKE UNIVERSITY · PI CROWLEY, STEVEN D · 2010 to 2018
$2.4M
Role of Gq Signaling in Promoting Podocyte Injury in Diabetes MellitusR01DK087707 · NIDDK · DUKE UNIVERSITY · PI SPURNEY, ROBERT · 2011 to 2014
$1.4M
The role of the M1 macrophage response in the progression of chronic kidney diseaseI01BX000893 · VA · DURHAM VA MEDICAL CENTER · PI Steven D Crowley · 2012 to 2026
–
BLRD VA I01 BX000893NIDDK NIH HHS DK087893-01NIDDK NIH HHS R01 DK087707NIDDK NIH HHS R01 DK087893
6 · The paper itself

Abstract

rationaleHuman clinical trials using type 1 angiotensin (AT(1)) receptor antagonists indicate that angiotensin II is a critical mediator of cardiovascular and renal disease. However, recent studies have suggested that individual tissue pools of AT(1) receptors may have divergent effects on target organ damage in hypertension.

objectiveWe examined the role of AT(1) receptors on T lymphocytes in the pathogenesis of hypertension and its complications. METHODS AND

resultsDeficiency of AT(1) receptors on T cells potentiated kidney injury during hypertension with exaggerated renal expression of chemokines and enhanced accumulation of T cells in the kidney. Kidneys and purified CD4(+) T cells from "T cell knockout" mice lacking AT(1) receptors on T lymphocytes had augmented expression of Th1-associated cytokines including interferon-γ and tumor necrosis factor-α. Within T lymphocytes, the transcription factors T-bet and GATA-3 promote differentiation toward the Th1 and Th2 lineages, respectively, and AT(1) receptor-deficient CD4(+) T cells had enhanced T-bet/GATA-3 expression ratios favoring induction of the Th1 response. Inversely, mice that were unable to mount a Th1 response due to T-bet deficiency were protected from kidney injury in our hypertension model.

conclusionsThe current studies identify an unexpected role for AT(1) receptors on T lymphocytes to protect the kidney in the setting of hypertension by favorably modulating CD4(+) T helper cell differentiation.

Indexed as

AnimalsCD4-Positive T-LymphocytesCell DifferentiationHypertensionKidneyMiceMice, 129 StrainMice, Inbred C57BLMice, KnockoutReceptor, Angiotensin, Type 1Receptor, Angiotensin, Type 1

Identifiers

PMID22534490
PMCPMC3393036
OpenAlexW2127832154

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

Registered trials

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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.