A novel chondrocyte sheet fabrication using human-induced pluripotent stem cell-derived expandable limb-bud mesenchymal cells.


Journal

Stem cell research & therapy
ISSN: 1757-6512
Titre abrégé: Stem Cell Res Ther
Pays: England
ID NLM: 101527581

Informations de publication

Date de publication:
24 02 2023
Historique:
received: 12 09 2022
accepted: 09 02 2023
entrez: 24 2 2023
pubmed: 25 2 2023
medline: 3 3 2023
Statut: epublish

Résumé

Cell sheet fabrication for articular cartilage regenerative medicine necessitates a large number of chondrocytes of consistent quality as a cell source. Previously, we have developed human-induced pluripotent stem cell (iPSC)-derived expandable PRRX1 ExpLBM cells derived from human-induced pluripotent stem cells (hiPSCs), including 414C2 and Ff-KVs09 (HLA homozygous), were seeded onto a culture plate and two-dimensional chondrogenic induction (2-DCI) was initiated. After 2-DCI, ExpLBM-derived chondrocytes were stripped and transferred to temperature-responsive culture inserts and the chondrocyte sheets were histologically examined or transplanted into osteochondral knee defects of immunodeficient rats. Immunohistochemistry revealed that ExpLBM-derived cell sheets were positive for Safranin O, COL2, and ACAN but that they were negative for COL1 and RUNX2. Furthermore, the engrafted tissues in osteochondral knee defects in immunodeficient rats were stained with SafO, human VIMENTIN, ACAN, and COL2. The present study is the first to report the chondrocyte sheet fabrication with hiPSC-derived cell source. hiPSC-derived ExpLBM would be a promising cell source for cell sheet technology in articular cartilage regenerative medicine.

Sections du résumé

BACKGROUND
Cell sheet fabrication for articular cartilage regenerative medicine necessitates a large number of chondrocytes of consistent quality as a cell source. Previously, we have developed human-induced pluripotent stem cell (iPSC)-derived expandable PRRX1
METHODS
ExpLBM cells derived from human-induced pluripotent stem cells (hiPSCs), including 414C2 and Ff-KVs09 (HLA homozygous), were seeded onto a culture plate and two-dimensional chondrogenic induction (2-DCI) was initiated. After 2-DCI, ExpLBM-derived chondrocytes were stripped and transferred to temperature-responsive culture inserts and the chondrocyte sheets were histologically examined or transplanted into osteochondral knee defects of immunodeficient rats.
RESULTS
Immunohistochemistry revealed that ExpLBM-derived cell sheets were positive for Safranin O, COL2, and ACAN but that they were negative for COL1 and RUNX2. Furthermore, the engrafted tissues in osteochondral knee defects in immunodeficient rats were stained with SafO, human VIMENTIN, ACAN, and COL2.
CONCLUSIONS
The present study is the first to report the chondrocyte sheet fabrication with hiPSC-derived cell source. hiPSC-derived ExpLBM would be a promising cell source for cell sheet technology in articular cartilage regenerative medicine.

Identifiants

pubmed: 36829201
doi: 10.1186/s13287-023-03252-4
pii: 10.1186/s13287-023-03252-4
pmc: PMC9960196
doi:

Substances chimiques

PRRX1 protein, human 0
Homeodomain Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

34

Informations de copyright

© 2023. The Author(s).

Références

N Engl J Med. 1994 Oct 6;331(14):889-95
pubmed: 8078550
Philos Trans R Soc Lond B Biol Sci. 2018 Jul 5;373(1750):
pubmed: 29786553
Biomaterials. 1995 Mar;16(4):297-303
pubmed: 7772669
Clin Orthop Relat Res. 2010 Jan;468(1):147-57
pubmed: 19653049
Am J Sports Med. 2009 Nov;37 Suppl 1:10S-19S
pubmed: 19846694
Biomaterials. 2014 Feb;35(7):2199-206
pubmed: 24360579
Cartilage. 2013 Jul;4(3 Suppl):5S-12S
pubmed: 26069664
Instr Course Lect. 2005;54:465-80
pubmed: 15952258
J Bone Joint Surg Am. 2004 Mar;86-A Suppl 1:65-72
pubmed: 14996923
Biomaterials. 2012 Jul;33(21):5278-86
pubmed: 22551484
J Biomed Mater Res. 1993 Oct;27(10):1243-51
pubmed: 8245039
Nat Biomed Eng. 2021 Aug;5(8):926-940
pubmed: 34373601
Development. 2020 Jun 19;147(12):
pubmed: 32561665
Am J Sports Med. 2010 Jun;38(6):1125-33
pubmed: 20360608
NPJ Regen Med. 2019 Feb 21;4:4
pubmed: 30820353
Instr Course Lect. 1998;47:487-504
pubmed: 9571450
Biochem Biophys Res Commun. 2006 Oct 20;349(2):723-31
pubmed: 16949051
Bone. 2015 Nov;80:14-18
pubmed: 26453494
Cell Stem Cell. 2019 Apr 4;24(4):566-578.e7
pubmed: 30853558
J Tissue Eng Regen Med. 2018 Oct;12(10):2067-2076
pubmed: 30058138

Auteurs

Tomoka Takao (T)

Department of Regenerative Science, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine, 2-5-1 Shikata-Cho, Kita-Ku, Okayama, 700-8558, Japan.

Masato Sato (M)

Department of Orthopaedic Surgery, Surgical Science, Tokai University School of Medicine, Isehara, Japan.

Yuki Fujisawa (Y)

Department of Regenerative Science, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine, 2-5-1 Shikata-Cho, Kita-Ku, Okayama, 700-8558, Japan.

Eriko Toyoda (E)

Department of Orthopaedic Surgery, Surgical Science, Tokai University School of Medicine, Isehara, Japan.

Daisuke Yamada (D)

Department of Regenerative Science, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine, 2-5-1 Shikata-Cho, Kita-Ku, Okayama, 700-8558, Japan.

Yukio Hitsumoto (Y)

Department of Regenerative Science, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine, 2-5-1 Shikata-Cho, Kita-Ku, Okayama, 700-8558, Japan.

Eiji Nakata (E)

Department Orthopedic Surgery, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine, Okayama, 700-8558, Japan.

Toshifumi Ozaki (T)

Department Orthopedic Surgery, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine, Okayama, 700-8558, Japan.

Takeshi Takarada (T)

Department of Regenerative Science, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine, 2-5-1 Shikata-Cho, Kita-Ku, Okayama, 700-8558, Japan. takarada@okayama-u.ac.jp.

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Classifications MeSH