Evidence map›Paper›PMID 36490356›Full record

ArticleBlood advances2023

Evidence of in vivo exogen protein uptake by red blood cells: a putative therapeutic concept.

Laura Hertz, Daniel Flormann, Lutz Birnbaumer, Christian Wagner, Matthias W Laschke, Lars Kaestner

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Blood advances, 2023. 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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
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  9. Big Data in Transfusion Medicine and Artificial Intelligence Analysis for Red Blood Cell Quality Control.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2023
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 4 countries.

Laura HertzTheoretical Medicine and Biosciences, Medical Faculty, Saarland University, Homburg, Germany.
Daniel FlormannDynamics of Fluids, Experimental Physics, Saarland University, Saarbruecken, Germany.ORCID 0000-0003-0869-6850
Lutz BirnbaumerInstitute of Biomedical Research (BIOMED), Catholic University of Argentina, Buenos Aires, Argentina.ORCID 0000-0002-0775-8661
Christian WagnerDynamics of Fluids, Experimental Physics, Saarland University, Saarbruecken, Germany.ORCID 0000-0001-7788-4594
Matthias W LaschkeMedical Faculty, Institute for Clinical and Experimental Surgery, Saarland University, Homburg, Germany.ORCID 0000-0002-7847-8456
Lars KaestnerTheoretical Medicine and Biosciences, Medical Faculty, Saarland University, Homburg, Germany.ORCID 0000-0001-6796-9535
Saarland University · DEPontificia Universidad Católica Argentina · ARUniversity of Luxembourg · LU

Funding

Transmembrane Signaling Mechanisms Involving TRP ChannelsZ01ES101684 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI BIRNBAUMER, LUTZ · 2003 to 2008
$2.1M
Intramural NIH HHS Z01 ES101684
6 · The paper itself

Abstract

For some molecular players in red blood cells (RBCs), the functional indications and molecular evidence are discrepant. One such protein is transient receptor potential channel of canonical subfamily, member 6 (TRPC6). Transcriptome analysis of reticulocytes revealed the presence of TRPC6 in mouse RBCs and its absence in human RBCs. We transfused TRPC6 knockout RBCs into wild-type mice and performed functional tests. We observed the "rescue" of TRPC6 within 10 days; however, the "rescue" was slower in splenectomized mice. The latter finding led us to mimic the mechanical challenge with the cantilever of an atomic force microscope and simultaneously carry out imaging by confocal (3D) microscopy. We observed the strong interaction of RBCs with the opposed surface at around 200 pN and the formation of tethers. The results of both the transfusion experiments and the atomic force spectroscopy suggest mechanically stimulated protein transfer to RBCs as a protein source in the absence of the translational machinery. This protein transfer mechanism has the potential to be utilized in therapeutic contexts, especially for hereditary diseases involving RBCs, such as hereditary xerocytosis or Gárdos channelopathy.

Indexed as

Anemia, Hemolytic, CongenitalErythrocytesAnimalsBlood TransfusionHumansHydrops FetalisMiceTRPC6 Cation ChannelTRPC6 Cation ChannelTRPC6 protein, humanTrpc6 protein, mouse

Identifiers

PMID36490356
PMCPMC10036505
OpenAlexW4311020131

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.