Evidence map›Paper›PMID 35012671›Full record

ArticleStem cell research & therapy2022

Optimization of human umbilical cord blood-derived mesenchymal stem cell isolation and culture methods in serum- and xeno-free conditions.

Liem Thanh Nguyen, Nghia Trung Tran, Uyen Thi Trang Than, Minh Quang Nguyen, Anh Minh Tran, Phuong Thi Xuan Do, Thao Thi Chu, Tu Dac Nguyen, Anh Viet Bui, Tien Anh Ngo and 2 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
5.4field-weighted citation impact, top 4% 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

27 citing papers in PubMed, 2 syntheses or guidelines pooled it, 36 citations in OpenAlex.

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  20. Mesenchymal stromal/stem cells and bronchopulmonary dysplasia.Frontiers in cell and developmental biology · 2023
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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

12 authors at 2 institutions in 2 countries.

Liem Thanh NguyenVinmec Research Institute of Stem Cell and Gene Technology, Hanoi, Vietnam.
Nghia Trung TranVinmec Research Institute of Stem Cell and Gene Technology, Hanoi, Vietnam.
Uyen Thi Trang ThanCenter of Applied sciences, Regenerative medicine, and Advance technologies (CARA), Hanoi, Vietnam.
Minh Quang NguyenVinmec Research Institute of Stem Cell and Gene Technology, Hanoi, Vietnam.
Anh Minh TranVNU University of Science, Vietnam National University, Hanoi, Vietnam.
Phuong Thi Xuan DoVinmec Research Institute of Stem Cell and Gene Technology, Hanoi, Vietnam.
Thao Thi ChuCenter of Applied sciences, Regenerative medicine, and Advance technologies (CARA), Hanoi, Vietnam.
Tu Dac NguyenCenter of Applied sciences, Regenerative medicine, and Advance technologies (CARA), Hanoi, Vietnam.
Anh Viet BuiCenter of Applied sciences, Regenerative medicine, and Advance technologies (CARA), Hanoi, Vietnam.
Tien Anh NgoCenter of Applied sciences, Regenerative medicine, and Advance technologies (CARA), Hanoi, Vietnam.
Van Thanh HoangVinmec Research Institute of Stem Cell and Gene Technology, Hanoi, Vietnam.
Nhung Thi My HoangVinmec Research Institute of Stem Cell and Gene Technology, Hanoi, Vietnam. hoangthimynhung@hus.edu.vn.ORCID 0000-0003-1717-1570
Vietnam National University, Hanoi · VNVinmec International Hospital · VN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough umbilical cord blood (UCB) is identified as a source of mesenchymal stem cells (MSCs) with various advantages, the success in cell isolation is volatile. Therefore, it is necessary to optimize methods of cord blood-derived MSC (UCB-MSC) isolation and culture. In this study, we evaluated the efficiency of UCB-MSC isolation and expansion using different commercially available serum- and xeno-free media and investigated the capacity of autologous serum and plasma as a supplement to support cell proliferation. Additionally, we defined the presence of multilineage-differentiating stress-enduring (Muse) cells in the UCB-MSC population. Functions of UCB-MSC in in vitro angiogenesis processes and anti-cancer were also verified.

methodsMononuclear cells were isolated using density gradient separation and cultured in four commercial media kits, as well as four surface coating solutions. UCB-MSCs were characterized and tested on tube formation assay, and co-cultured with SK-MEL cells in a transwell system.

resultsThe results showed that only StemMACS™ MSC Expansion Media is more appropriate to isolate and culture UCB-MSCs. The cells exhibited a high cell proliferation rate, CFU forming capability, MSC surface marker expression, trilineage differentiate potential, and chromosome stability. In addition, the culture conditions with autologous serum coating and autologous plasma supplement enhanced cell growth and colony forming. This cell population contained Muse cells at rate of 0.3%. Moreover, UCB-MSCs could induce the tube formation of human umbilical vein endothelial cells and inhibit more than 50% of SK-MEL cell growth.

conclusionsUCB-MSCs could be high-yield isolated and expanded under serum- and xeno-free conditions by using the StemMACS™ MSC Expansion Media kit. Autologous serum coating and plasma supplement enhanced cell proliferation. These UCB-MSCs had effected the tube formation process and an anti-cancer impact.

Indexed as

Fetal BloodMesenchymal Stem CellsCell Culture TechniquesCell DifferentiationCell ProliferationCells, CulturedCell SeparationEndothelial CellsHumansUmbilical CordAngiogenesisAutologous plasmaCancer cellsMesenchymal stem cellsMuse cellsUmbilical cord blood

Identifiers

PMID35012671
PMCPMC8751356
OpenAlexW4205404257

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.