Evidence map›Paper›PMID 34505405›Full record

ArticleStem cells translational medicine2021

A scalable system for generation of mesenchymal stem cells derived from induced pluripotent cells employing bioreactors and degradable microcarriers.

Robert E Rogers, Andrew Haskell, Berkley P White, Sujata Dalal, Megan Lopez, Daniel Tahan, Simin Pan, Gagandeep Kaur, Hyemee Kim, Heather Barreda and 11 more

Open access · goldAbstract read
In one paragraph

Article in Stem cells translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-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

18 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Biomaterials for Cell Manufacturing.ACS macro letters · 2024
    Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Science advances · 2023
    Article
  12. Article
  13. Bioreactor Technologies for Enhanced Organoid Culture.International journal of molecular sciences · 2023
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. 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

21 authors at 3 institutions in 1 country.

Robert E RogersDepartment of Molecular and Cellular Medicine, Texas A&M Health Science Center, College of Medicine, Bryan, Texas, USA.ORCID 0000-0001-5578-6993
Andrew HaskellDepartment of Molecular and Cellular Medicine, Texas A&M Health Science Center, College of Medicine, Bryan, Texas, USA.ORCID 0000-0003-1170-2254
Berkley P WhiteDepartment of Biomedical Engineering, Texas A&M University, Emerging Technologies Building, College Station, Texas, USA.
Sujata DalalDepartment of Molecular and Cellular Medicine, Texas A&M Health Science Center, College of Medicine, Bryan, Texas, USA.
Megan LopezDepartment of Molecular and Cellular Medicine, Texas A&M Health Science Center, College of Medicine, Bryan, Texas, USA.
Daniel TahanDepartment of Molecular and Cellular Medicine, Texas A&M Health Science Center, College of Medicine, Bryan, Texas, USA.
Simin PanDepartment of Molecular and Cellular Medicine, Texas A&M Health Science Center, College of Medicine, Bryan, Texas, USA.
Gagandeep KaurDepartment of Molecular and Cellular Medicine, Texas A&M Health Science Center, College of Medicine, Bryan, Texas, USA.
Hyemee KimDepartment of Molecular and Cellular Medicine, Texas A&M Health Science Center, College of Medicine, Bryan, Texas, USA.
Heather BarredaDepartment of Molecular and Cellular Medicine, Texas A&M Health Science Center, College of Medicine, Bryan, Texas, USA.
Susan L WoodardNational Center for Therapeutics Manufacturing, Texas A&M University, College Station, Texas, USA.
Oscar R BenavidesDepartment of Biomedical Engineering, Texas A&M University, Emerging Technologies Building, College Station, Texas, USA.
Jing DaiDepartment of Electrical and Computer Engineering, Texas A&M University, Wisenbaker Engineering Building, College Station, Texas, USA.
Qingguo ZhaoDepartment of Molecular and Cellular Medicine, Texas A&M Health Science Center, College of Medicine, Bryan, Texas, USA.
Kristen C MaitlandDepartment of Biomedical Engineering, Texas A&M University, Emerging Technologies Building, College Station, Texas, USA.ORCID 0000-0003-0931-0622
Arum HanDepartment of Biomedical Engineering, Texas A&M University, Emerging Technologies Building, College Station, Texas, USA.
Zivko L NikolovNational Center for Therapeutics Manufacturing, Texas A&M University, College Station, Texas, USA.
Fei LiuDepartment of Molecular and Cellular Medicine, Texas A&M Health Science Center, College of Medicine, Bryan, Texas, USA.
Ryang Hwa LeeDepartment of Molecular and Cellular Medicine, Texas A&M Health Science Center, College of Medicine, Bryan, Texas, USA.
Carl A GregoryDepartment of Molecular and Cellular Medicine, Texas A&M Health Science Center, College of Medicine, Bryan, Texas, USA.ORCID 0000-0001-6444-5541
Roland KaunasDepartment of Biomedical Engineering, Texas A&M University, Emerging Technologies Building, College Station, Texas, USA.ORCID 0000-0001-6748-1126
Texas A&M Health Science Center · USTexas College · USTexas A&M University · US

Funding

Advanced Methods for Mimicking the Osteogenic Niche to Heal BoneR01AR066033 · NIAMS · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI GREGORY, CARL A. · 2014 to 2017
$1.3M
Therapeutic effects of MSC-derived extracellular vesicles on Sjögren's SyndromeR21DE027457 · NIDCR · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI LEE, RYANG HWA, LIU, FEI · 2018 to 2019
$408k
NIAMS NIH HHS R01 AR066033NIDCR NIH HHS R21 DE027457
6 · The paper itself

Abstract

Human mesenchymal stem cells (hMSCs) are effective in treating disorders resulting from an inflammatory or heightened immune response. The hMSCs derived from induced pluripotent stem cells (ihMSCs) share the characteristics of tissue derived hMSCs but lack challenges associated with limited tissue sources and donor variation. To meet the expected future demand for ihMSCs, there is a need to develop scalable methods for their production at clinical yields while retaining immunomodulatory efficacy. Herein, we describe a platform for the scalable expansion and rapid harvest of ihMSCs with robust immunomodulatory activity using degradable gelatin methacryloyl (GelMA) microcarriers. GelMA microcarriers were rapidly and reproducibly fabricated using a custom microfluidic step emulsification device at relatively low cost. Using vertical wheel bioreactors, 8.8 to 16.3-fold expansion of ihMSCs was achieved over 8 days. Complete recovery by 5-minute digestion of the microcarriers with standard cell dissociation reagents resulted in >95% viability. The ihMSCs matched or exceeded immunomodulatory potential in vitro when compared with ihMSCs expanded on monolayers. This is the first description of a robust, scalable, and cost-effective method for generation of immunomodulatory ihMSCs, representing a significant contribution to their translational potential.

Indexed as

Induced Pluripotent Stem CellsMesenchymal Stem CellsBioreactorsCell Culture TechniquesCell DifferentiationCell ProliferationGelatinHumansMethacrylatesGelatingelatin methacryloylMethacrylatesbioreactorimmunomodulatoryinduced pluripotent stem cellsmesenchymal stem cells

Identifiers

PMID34505405
PMCPMC8641084
OpenAlexW3197111581

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.