Evidence map›Paper›PMID 26611568›Full record

ArticleScientific reports2015

Accelerated apoptotic death and in vivo turnover of erythrocytes in mice lacking functional mitogen- and stress-activated kinase MSK1/2.

Elisabeth Lang, Rosi Bissinger, Abul Fajol, Madhuri S Salker, Yogesh Singh, Christine Zelenak, Mehrdad Ghashghaeinia, Shuchen Gu, Kashif Jilani, Adrian Lupescu and 8 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

13 citing papers in PubMed, 50 citations in OpenAlex.

  1. Cellular Mechanisms Enabling Mitochondria Transfer and Transplantation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  2. Review
  3. Review
  4. Article
  5. Casein kinase 1α mediates eryptosis: a review.Apoptosis : an international journal on programmed cell death · 2023
    Review
  6. LRRC8A-containing chloride channel is crucial for cell volume recovery and survival under hypertonic conditions.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  7. Ion Transport in Eryptosis, the Suicidal Death of Erythrocytes.Frontiers in cell and developmental biology · 2020
    Review
  8. Article
  9. Manipulating Eryptosis of Human Red Blood Cells: A Novel Antimalarial Strategy?Frontiers in cellular and infection microbiology · 2018
    Review
  10. Article
  11. Article
  12. Article
  13. 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

18 authors at 5 institutions in 5 countries.

Elisabeth LangDepartment of Physiology, University of Tübingen, Gmelinstr. 5, 72076 Tübingen, Germany.
Rosi BissingerDepartment of Physiology, University of Tübingen, Gmelinstr. 5, 72076 Tübingen, Germany.
Abul FajolDepartment of Physiology, University of Tübingen, Gmelinstr. 5, 72076 Tübingen, Germany.
Madhuri S SalkerDepartment of Physiology, University of Tübingen, Gmelinstr. 5, 72076 Tübingen, Germany.
Yogesh SinghDepartment of Physiology, University of Tübingen, Gmelinstr. 5, 72076 Tübingen, Germany.
Christine ZelenakCharité Medical University Berlin, Charitéplatz 1, 10117 Berlin, Germany.
Mehrdad GhashghaeiniaDepartment of Physiology, University of Tübingen, Gmelinstr. 5, 72076 Tübingen, Germany.
Shuchen GuDepartment of Physiology, University of Tübingen, Gmelinstr. 5, 72076 Tübingen, Germany.
Kashif JilaniDepartment of Physiology, University of Tübingen, Gmelinstr. 5, 72076 Tübingen, Germany.
Adrian LupescuDepartment of Physiology, University of Tübingen, Gmelinstr. 5, 72076 Tübingen, Germany.
Kathleen M S E ReyskensMRC Phosphorylation Unit, University of Dundee, Dow Street, Dundee DD1 5EH, United Kingdom.
Teresa F AckermannDepartment of Physiology, University of Tübingen, Gmelinstr. 5, 72076 Tübingen, Germany.
Michael FöllerDepartment of Physiology, University of Tübingen, Gmelinstr. 5, 72076 Tübingen, Germany.
Erwin SchleicherDepartment of Internal Medicine, University of Tübingen, Otfried-Müller-Straβe 10, 72076 Tübingen, Germany.
William P SheffieldDepartment of Pathology and Molecular Medicine, McMaster University, 1280 Main Street West, Hamilton, Ontario L8S4K1, Canada.
J Simon C ArthurMRC Phosphorylation Unit, University of Dundee, Dow Street, Dundee DD1 5EH, United Kingdom.
Florian LangDepartment of Physiology, University of Tübingen, Gmelinstr. 5, 72076 Tübingen, Germany.
Syed M QadriDepartment of Physiology, University of Tübingen, Gmelinstr. 5, 72076 Tübingen, Germany.
University of Tübingen · DEUniversity of Dundee · GBCharité - Universitätsmedizin Berlin · DEMcMaster University · CAZhejiang University · CN

Funding

Arthritis Research UK 20409Medical Research Council MR/L008785/1
6 · The paper itself

Abstract

The mitogen- and stress-activated kinase MSK1/2 plays a decisive role in apoptosis. In analogy to apoptosis of nucleated cells, suicidal erythrocyte death called eryptosis is characterized by cell shrinkage and cell membrane scrambling leading to phosphatidylserine (PS) externalization. Here, we explored whether MSK1/2 participates in the regulation of eryptosis. To this end, erythrocytes were isolated from mice lacking functional MSK1/2 (msk(-/-)) and corresponding wild-type mice (msk(+/+)). Blood count, hematocrit, hemoglobin concentration and mean erythrocyte volume were similar in both msk(-/-) and msk(+/+) mice, but reticulocyte count was significantly increased in msk(-/-) mice. Cell membrane PS exposure was similar in untreated msk(-/-) and msk(+/+) erythrocytes, but was enhanced by pathophysiological cell stressors ex vivo such as hyperosmotic shock or energy depletion to significantly higher levels in msk(-/-) erythrocytes than in msk(+/+) erythrocytes. Cell shrinkage following hyperosmotic shock and energy depletion, as well as hemolysis following decrease of extracellular osmolarity was more pronounced in msk(-/-) erythrocytes. The in vivo clearance of autologously-infused CFSE-labeled erythrocytes from circulating blood was faster in msk(-/-) mice. The spleens from msk(-/-) mice contained a significantly greater number of PS-exposing erythrocytes than spleens from msk(+/+) mice. The present observations point to accelerated eryptosis and subsequent clearance of erythrocytes leading to enhanced erythrocyte turnover in MSK1/2-deficient mice.

Indexed as

AnimalsApoptosisErythrocyte IndicesErythrocytesFemaleGene ExpressionHematocritHemoglobinsHemolysisHumansMaleMiceMice, KnockoutOsmotic FragilityOsmotic PressurePhosphatidylserinesHemoglobinsmitogen and stress-activated protein kinase 1PhosphatidylserinesRibosomal Protein S6 Kinases, 90-kDaRps6ka4 protein, mouse

Identifiers

PMID26611568
PMCPMC4661433
OpenAlexW2175884225

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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.