Evidence map›Paper›PMID 41551934›Full record

ArticleStem cells international2026

The Size of Human Mesenchymal Tissue Stem Cell Turnover Units is a Major Determinant for Maintaining High Stem Cell Fractions With Serial Culture Expansion.

James L Sherley, Chen Cao, Celia Sommer, Alex Dahlkemper, James Sugai, Hitesh Chopra, Darnell Kaigler

Abstract read
In one paragraph

Article in Stem cells international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

7 authors.

James L SherleyAsymmetrex LLC, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0002-9711-3751
Chen CaoDepartment of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, Michigan, USA, umich.edu.ORCID https://orcid.org/0000-0001-7717-0882
Celia SommerDepartment of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, Michigan, USA, umich.edu.
Alex DahlkemperDepartment of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, Michigan, USA, umich.edu.
James SugaiDepartment of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, Michigan, USA, umich.edu.
Hitesh ChopraDepartment of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, Michigan, USA, umich.edu.
Darnell KaiglerDepartment of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, Michigan, USA, umich.edu.ORCID https://orcid.org/0000-0003-3728-4310

Funding

Mechanisms of dental pulp stem cell differentiation into functional endotheliumR01DE021410 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NOR, JACQUES EDUARDO · 2011 to 2021
$3.2M
Redefining mesenchymal stem cells: using their cellular and molecular phenotypes to determine their regenerative and therapeutic propertiesR01DE028657 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KAIGLER, DARNELL · 2019 to 2023
$2.1M
Design and production of an automated electronic tissue stem cell counterR44HL154900 · NHLBI · ASYMMETREX, LLC · PI SHERLEY, JAMES L · 2024 to 2025
$1.8M
Regulation of dental pulp stem cell fateR37DE021410 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Jacques Eduardo Nor · 2024 to 2026
$1.2M
Increased Validation of a First Method for Counting Tissue Stem Cells SpecificallyR43HL154900 · NHLBI · ASYMMETREX, LLC · PI SHERLEY, JAMES L · 2020 to 2020
$420k
NHLBI NIH HHS R43 HL154900NHLBI NIH HHS R44 HL154900NIDCR NIH HHS R01 DE021410NIDCR NIH HHS R01 DE028657NIDCR NIH HHS R37 DE021410
6 · The paper itself

Abstract

Recently, we used kinetic stem cell (KSC) counting to show that the stability of the stem cell fraction (SCF) during serial culture expansion of human oral alveolar bone mesenchymal tissue cell (MTC) preparations varied significantly among patient donors. Whereas some patient donor samples' SCFs declined rapidly, others showed a moderate decrease; and still others had highly stable SCFs during serial culture expansion. Defining the cell kinetics basis for these differences in SCF stability could lead to effective solutions for the problem of loss of mesenchymal stem cell (MSC) function when MTC preparations are expanded for research and clinical applications. Using KSC counting, we show that greater SCF stability is associated with smaller stem cell turnover units, which reduce the SCF by cell dilution. This finding confirms earlier evidence and proposals that, by limiting the production and proliferation of committed progenitor cells, more effective expansion of tissue stem cells, such as MSCs, can be achieved. Because of the universal nature of tissue stem cell turnover units and the continuation of their basic cell kinetics programs in in vitro cell culture, the effects defined herein are predicted to apply to other types of human tissue stem cells of interest for stem cell medicine.

Indexed as

alveolar boneasymmetric self-renewalcell lineageexpansion culturemesenchymal stem cellstissue stem cellsturnover unit

Identifiers

PMID41551934
PMCPMC12811402

What OpenQuestion 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 OpenQuestion graph.