Evidence map›Paper›PMID 37088551›Full record

ArticleCell proliferation2023

Baffled-flow culture system enables the mass production of megakaryocytes from human embryonic stem cells by enhancing mitochondrial function.

Xumin Wu, Bowen Zhang, Keyi Chen, Jiahui Zhao, Yunxing Li, Jisheng Li, Chuanli Liu, Lijuan He, Tao Fan, Chao Wang and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell proliferation, 2023. 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
6.7field-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

7 citing papers in PubMed, 15 citations in OpenAlex.

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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

13 authors at 3 institutions in 3 countries.

Xumin WuSchool of Pharmacy, Guizhou University, Guiyang, China.
Bowen ZhangStem Cell and Regenerative Medicine Lab, Beijing Institute of Radiation Medicine, Beijing, China.
Keyi ChenStem Cell and Regenerative Medicine Lab, Beijing Institute of Radiation Medicine, Beijing, China.
Jiahui ZhaoStem Cell and Regenerative Medicine Lab, Beijing Institute of Radiation Medicine, Beijing, China.
Yunxing LiStem Cell and Regenerative Medicine Lab, Beijing Institute of Radiation Medicine, Beijing, China.
Jisheng LiStem Cell and Regenerative Medicine Lab, Beijing Institute of Radiation Medicine, Beijing, China.ORCID https://orcid.org/0000-0001-9109-5815
Chuanli LiuStem Cell and Regenerative Medicine Lab, Beijing Institute of Radiation Medicine, Beijing, China.
Lijuan HeSouth China Research Center for Stem Cell & Regenerative Medicine, SCIB, Guangzhou, China.
Tao FanStem Cell and Regenerative Medicine Lab, Beijing Institute of Radiation Medicine, Beijing, China.
Chao WangStem Cell and Regenerative Medicine Lab, Beijing Institute of Radiation Medicine, Beijing, China.
Yan LiSchool of Pharmacy, Guizhou University, Guiyang, China.
Xuetao PeiStem Cell and Regenerative Medicine Lab, Beijing Institute of Radiation Medicine, Beijing, China.
Yanhua LiStem Cell and Regenerative Medicine Lab, Beijing Institute of Radiation Medicine, Beijing, China.ORCID https://orcid.org/0000-0001-5584-9376
Guizhou University · CNInstitute for Stem Cell Biology and Regenerative Medicine · INGuangzhou Regenerative Medicine and Health Guangdong Laboratory · CN

Funding

National Natural Science Foundation of China 32200589National Natural Science Foundation of China 81800103National Natural Science Foundation of China 81872553National Natural Science Foundation of China 82200122National Natural Science Foundation of China 82270132
6 · The paper itself

Abstract

Human embryonic stem cells (hESCs) have become an ideal cell source for the ex vivo generation of megakaryocyte (MK) and platelet products for clinical applications. However, an ongoing challenge is to establish scalable culture systems to maximize the yield of stem cell-derived MKs that release platelets. We defined a specific dynamic 3D manufacturing system in a baffled-flow manner that could remarkably facilitate megakaryopoiesis and increase the yield of platelet-producing MKs from hESCs within a 12-day induction period. Additionally, an increased number of >16N ploidy MKs, proplatelets, and platelets were generated from induced cells harvested on Day 12 using the specific dynamic culture method. The specific dynamic culture method significantly enhanced endothelium-to-haematopoietic transition and early haematopoiesis. More importantly, MK fate was significantly facilitated in a specific dynamic manner during early haematopoiesis. Mechanistically, this dynamic culture significantly enhanced mitochondrial function via the oxidative phosphorylation pathway and caused differentiation skewing of hESCs toward megakaryopoiesis. This study can aid in the automatic and scalable production of MKs from stem cells using baffled-flow bioreactors and assist in the manufacturing of hESC-derived MK and platelet products.

Indexed as

Human Embryonic Stem CellsMegakaryocytesBlood PlateletsCell DifferentiationHumansMitochondria

Identifiers

PMID37088551
PMCPMC10693187
OpenAlexW4366783485

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.