Evidence map›Paper›PMID 32929449›Full record

ArticleBlood2020

Bone marrow regeneration requires mitochondrial transfer from donor Cx43-expressing hematopoietic progenitors to stroma.

Karin Golan, Abhishek K Singh, Orit Kollet, Mayla Bertagna, Mark J Althoff, Eman Khatib-Massalha, Ekaterina Petrovich-Kopitman, Ashley M Wellendorf, Hassan Massalha, Smadar Levin-Zaidman and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
5.8field-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

64 citing papers in PubMed, 87 citations in OpenAlex.

  1. Article
  2. Chemotherapy-induced thrombocytopenia: from "platelet counting" to ecological repair of the bone marrow.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
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  16. Mitochondria transfer in tissue homeostasis and diseases.International journal of biological sciences · 2026
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4 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 3 countries.

Karin GolanDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Abhishek K SinghDivision of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Orit KolletDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Mayla BertagnaDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Mark J AlthoffDivision of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Eman Khatib-MassalhaDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Ekaterina Petrovich-KopitmanDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Ashley M WellendorfDivision of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Hassan MassalhaMolecular Cell Biology Department and.
Smadar Levin-ZaidmanDepartment of Chemical Research Support, Weizmann Institute of Science, Rehovot, Israel.
Tali DadoshDepartment of Chemical Research Support, Weizmann Institute of Science, Rehovot, Israel.
Breanna BohanHoxworth Blood Center, University of Cincinnati, Cincinnati, OH; and.
Mruniya V GawaliDivision of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Biplab DasguptaDivision of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Tsvee LapidotDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Jose A CancelasDivision of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Weizmann Institute of Science · ILCincinnati Children's Hospital Medical Center · USInstitute of Molecular and Cell Biology · RUUniversity of Cincinnati · US

Funding

Mitochondria mediated intercellular metabolic coupling in bone marrow regenerationR01DK124115 · NIDDK · DANA-FARBER CANCER INST · PI Jose A. Cancelas · 2020 to 2026
$1.9M
Scribble in hematopoietic stem cell activityF31HL132468 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI ALTHOFF, MARK JORDAN · 2016 to 2019
$147k
NHLBI NIH HHS F31 HL132468NIDDK NIH HHS R01 DK124115
6 · The paper itself

Abstract

The fate of hematopoietic stem and progenitor cells (HSPC) is tightly regulated by their bone marrow (BM) microenvironment (ME). BM transplantation (BMT) frequently requires irradiation preconditioning to ablate endogenous hematopoietic cells. Whether the stromal ME is damaged and how it recovers after irradiation is unknown. We report that BM mesenchymal stromal cells (MSC) undergo massive damage to their mitochondrial function after irradiation. Donor healthy HSPC transfer functional mitochondria to the stromal ME, thus improving mitochondria activity in recipient MSC. Mitochondrial transfer to MSC is cell-contact dependent and mediated by HSPC connexin-43 (Cx43). Hematopoietic Cx43-deficient chimeric mice show reduced mitochondria transfer, which was rescued upon re-expression of Cx43 in HSPC or culture with isolated mitochondria from Cx43 deficient HSPCs. Increased intracellular adenosine triphosphate levels activate the purinergic receptor P2RX7 and lead to reduced activity of adenosine 5'-monophosphate-activated protein kinase (AMPK) in HSPC, dramatically increasing mitochondria transfer to BM MSC. Host stromal ME recovery and donor HSPC engraftment were augmented after mitochondria transfer. Deficiency of Cx43 delayed mesenchymal and osteogenic regeneration while in vivo AMPK inhibition increased stromal recovery. As a consequence, the hematopoietic compartment reconstitution was improved because of the recovery of the supportive stromal ME. Our findings demonstrate that healthy donor HSPC not only reconstitute the hematopoietic system after transplantation, but also support and induce the metabolic recovery of their irradiated, damaged ME via mitochondria transfer. Understanding the mechanisms regulating stromal recovery after myeloablative stress are of high clinical interest to optimize BMT procedures and underscore the importance of accessory, non-HSC to accelerate hematopoietic engraftment.

Indexed as

RegenerationAnimalsBone MarrowConnexin 43Hematopoietic Stem CellsHumansMiceMitochondriaConnexin 43GJA1 protein, mouse

Identifiers

PMID32929449
PMCPMC7735163
OpenAlexW3087068058

What OpenQuestion holds

Textmetadata
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.