Evidence map›Paper›PMID 38330198›Full record

ArticleBlood advances2024

Altered platelet-megakaryocyte endocytosis and trafficking of albumin and fibrinogen in RUNX1 haplodeficiency.

Fabiola Del Carpio-Cano, Guangfen Mao, Lawrence E Goldfinger, Jeremy Wurtzel, Liying Guan, Mohammad Afaque Alam, Kiwon Lee, Mortimer Poncz, A Koneti Rao

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Transcription factor RUNX1 regulates coagulation factor XIII-A (Research and practice in thrombosis and haemostasis · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Fabiola Del Carpio-CanoSol Sherry Thrombosis Research Center, Lewis Katz School of Medicine at Temple University, Philadelphia, PA.
Guangfen MaoSol Sherry Thrombosis Research Center, Lewis Katz School of Medicine at Temple University, Philadelphia, PA.
Lawrence E GoldfingerDivision of Hematology, Department of Medicine, Cardeza Foundation for Hematologic Research, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA.ORCID 0000-0003-0525-6008
Jeremy WurtzelDivision of Hematology, Department of Medicine, Cardeza Foundation for Hematologic Research, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA.
Liying GuanSol Sherry Thrombosis Research Center, Lewis Katz School of Medicine at Temple University, Philadelphia, PA.ORCID 0000-0002-7470-564X
Mohammad Afaque AlamSol Sherry Thrombosis Research Center, Lewis Katz School of Medicine at Temple University, Philadelphia, PA.ORCID 0000-0001-5801-2512
Kiwon LeeDepartment of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA.ORCID 0000-0003-1340-3602
Mortimer PonczDepartment of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA.ORCID 0000-0001-7237-3613
A Koneti RaoSol Sherry Thrombosis Research Center, Lewis Katz School of Medicine at Temple University, Philadelphia, PA.ORCID 0000-0002-3078-7778
Temple University · USChildren's Hospital of Philadelphia · USThomas Jefferson University · US

Funding

New Mechanistic Insights & Therapeutic Applications of Megakaryocytes/PlateletsR35HL150698 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI Mortimer Poncz · 2020 to 2026
$7.3M
Human Platelet Defects in Transcription Factor RUNX1 HaplodeficiencyR01HL109568 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI RAO, ANGARA KONETI · 2013 to 2022
$3.4M
Novel small G protein pathway regulators of GPVI signaling in plateletsR01HL137207 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI GOLDFINGER, LAWRENCE E, KUNAPULI, SATYA P. · 2017 to 2020
$2.5M
Runx1 Haplodeficiency, Endocytosis and Vesicle transportR01HL137376 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI RAO, ANGARA KONETI · 2018 to 2021
$1.8M
Function and regulation of constitutive protein translation in plateletsR01HL159006 · NHLBI · THOMAS JEFFERSON UNIVERSITY · PI GOLDFINGER, LAWRENCE E · 2021 to 2024
$1.6M
NHLBI NIH HHS R01 HL109568NHLBI NIH HHS R01 HL137207NHLBI NIH HHS R01 HL137376NHLBI NIH HHS R01 HL159006NHLBI NIH HHS R35 HL150698
6 · The paper itself

Abstract

abstractPlatelet α-granules have numerous proteins, some synthesized by megakaryocytes (MK) and others not synthesized but incorporated by endocytosis, an incompletely understood process in platelets/MK. Germ line RUNX1 haplodeficiency, referred to as familial platelet defect with predisposition to myeloid malignancies (FPDMMs), is associated with thrombocytopenia, platelet dysfunction, and granule deficiencies. In previous studies, we found that platelet albumin, fibrinogen, and immunoglobulin G (IgG) were decreased in a patient with FPDMM. We now show that platelet endocytosis of fluorescent-labeled albumin, fibrinogen, and IgG is decreased in the patient and his daughter with FPDMM. In megakaryocytic human erythroleukemia (HEL) cells, small interfering RNA RUNX1 knockdown (KD) increased uptake of these proteins over 24 hours compared with control cells, with increases in caveolin-1 and flotillin-1 (2 independent regulators of clathrin-independent endocytosis), LAMP2 (a lysosomal marker), RAB11 (a marker of recycling endosomes), and IFITM3. Caveolin-1 downregulation in RUNX1-deficient HEL cells abrogated the increased uptake of albumin, but not fibrinogen. Albumin, but not fibrinogen, partially colocalized with caveolin-1. RUNX1 KD resulted in increased colocalization of albumin with flotillin and fibrinogen with RAB11, suggesting altered trafficking of both proteins. The increased uptake of albumin and fibrinogen, as well as levels of caveolin-1, flotillin-1, LAMP2, and IFITM3, were recapitulated by short hairpin RNA RUNX1 KD in CD34+-derived MK. To our knowledge, these studies provide first evidence that platelet endocytosis of albumin and fibrinogen is impaired in some patients with RUNX1-haplodeficiency and suggest that megakaryocytes have enhanced endocytosis with defective trafficking, leading to loss of these proteins by distinct mechanisms. This study provides new insights into mechanisms governing endocytosis and α-granule deficiencies in RUNX1-haplodeficiency.

Indexed as

Blood Coagulation Disorders, InheritedBlood Platelet DisordersHemostaticsLeukemia, Erythroblastic, AcuteLeukemia, Myeloid, AcuteAlbuminsCaveolin 1Core Binding Factor Alpha 2 SubunitEndocytosisFibrinogenHumansImmunoglobulin GMegakaryocytesMembrane ProteinsRNA-Binding ProteinsAlbuminsCaveolin 1Core Binding Factor Alpha 2 SubunitFibrinogenHemostaticsIFITM3 protein, humanImmunoglobulin GMembrane ProteinsRNA-Binding ProteinsRUNX1 protein, human

Identifiers

PMID38330198
PMCPMC10997914
OpenAlexW4391658164

What Socratic 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 Socratic graph.