Evidence map›Paper›PMID 35021601›Full record

ArticleHaematologica2022

Sorting nexin 24 is required for α-granule biogenesis and cargo delivery in megakaryocytes.

Joanne Lacey, Simon J Webster, Paul R Heath, Chris J Hill, Lucinda Nicholson-Goult, Bart E Wagner, Abdullah O Khan, Neil V Morgan, Michael Makris, Martina E Daly

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. FLI1 and GATA1 governHaematologica · 2025
    Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
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

10 authors at 3 institutions in 1 country.

Joanne LaceyDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.
Simon J WebsterDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.
Paul R HeathSheffield Institute for Translational Neuroscience (SITraN), Department of Neuroscience, University of Sheffield, Sheffield, UK.
Chris J HillDepartment of Molecular Biology and Biotechnology, University of Sheffield, Sheffield, UK.
Lucinda Nicholson-GoultHistopathology Department, Royal Hallamshire Hospital, Sheffield, UK.
Bart E WagnerHistopathology Department, Royal Hallamshire Hospital, Sheffield, UK.
Abdullah O KhanInstitute of Cardiovascular Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Neil V MorganInstitute of Cardiovascular Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Michael MakrisDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.
Martina E DalyDepartment of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK. M.Daly@sheffield.ac.uk.
University of Sheffield · GBRoyal Hallamshire Hospital · GBUniversity of Birmingham · GB

Funding

British Heart Foundation PG/15/61/31634Wellcome TrustWellcome Trust 218649/Z/19/Z
6 · The paper itself

Abstract

Germline defects affecting the DNA-binding domain of the transcription factor FLI1 are associated with a bleeding disorder that is characterized by the presence of large, fused α-granules in platelets. We investigated whether the genes showing abnormal expression in FLI1-deficient platelets could be involved in platelet α-granule biogenesis by undertaking transcriptome analysis of control platelets and platelets harboring a DNA-binding variant of FLI1. Our analysis identified 2,276 transcripts that were differentially expressed in FLI1-deficient platelets. Functional annotation clustering of the coding transcripts revealed significant enrichment for gene annotations relating to protein transport, and identified Sorting nexin 24 (SNX24) as a candidate for further investigation. Using an induced pluripotent stem cell-derived megakaryocyte model, SNX24 expression was found to be increased during the early stages of megakaryocyte differentiation and downregulated during proplatelet formation, indicating tight regulatory control during megakaryopoiesis. CRISPR-Cas9 mediated knockout (KO) of SNX24 led to decreased expression of immature megakaryocyte markers, CD41 and CD61, and increased expression of the mature megakaryocyte marker CD42b (P=0.0001), without affecting megakaryocyte polyploidisation, or proplatelet formation. Electron microscopic analysis revealed an increase in empty membrane-bound organelles in SNX24 KO megakaryocytes, a reduction in α-granules and an absence of immature and mature multivesicular bodies, consistent with a defect in the intermediate stage of α-granule maturation. Co-localization studies showed that SNX24 associates with each compartment of α-granule maturation. Reduced expression of CD62P and VWF was observed in SNX24 KO megakaryocytes. We conclude that SNX24 is required for α-granule biogenesis and intracellular trafficking of α-granule cargo within megakaryocytes.

Indexed as

MegakaryocytesSorting NexinsBlood PlateletsCytoplasmic GranulesDNAHumansProtein TransportDNASNX24 protein, humanSorting Nexins

Identifiers

PMID35021601
PMCPMC9335091
OpenAlexW4205642361

What Socratic holds

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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 Socratic graph.