Functional suppression accompanies internal mitochondrial reorganization during cellular reprogramming.

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Functional suppression accompanies internal mitochondrial reorganization during cellular reprogramming.
Συγγραφείς: Diak N; Department of Molecular Biology, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Medykow 18 Street, 40-752, Katowice, Poland., Sieroń L; Department of Molecular Biology, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Medykow 18 Street, 40-752, Katowice, Poland., Janelt K; Department of Molecular Biology, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Medykow 18 Street, 40-752, Katowice, Poland., Chajec L; Faculty of Natural Sciences, Institute of Biology, Biotechnology and Environmental Protection, University of Silesia in Katowice, Bankowa 9, 40-007, Katowice, Poland., Fus-Kujawa A; Department of Molecular Biology, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Medykow 18 Street, 40-752, Katowice, Poland., Dziedzic-Kowalska A; Department of Molecular Biology, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Medykow 18 Street, 40-752, Katowice, Poland., Trybus A; Department of Molecular Biology, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Medykow 18 Street, 40-752, Katowice, Poland., Raszczok K; Department of Molecular Biology, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Medykow 18 Street, 40-752, Katowice, Poland.; Students Scientific Society, Faculty of Medical Sciences, Medical University of Silesia, Katowice, Poland., Bajdak-Rusinek K; Department of Molecular Biology, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Medykow 18 Street, 40-752, Katowice, Poland. kbajdak-rusinek@sum.edu.pl.
Πηγή: Histochemistry and cell biology [Histochem Cell Biol] 2026 Apr 20; Vol. 164 (1). Date of Electronic Publication: 2026 Apr 20.
Τύπος έκδοσης: Journal Article
Γλώσσα: English
Στοιχεία περιοδικού: Publisher: Springer Country of Publication: Germany NLM ID: 9506663 Publication Model: Electronic Cited Medium: Internet ISSN: 1432-119X (Electronic) Linking ISSN: 09486143 NLM ISO Abbreviation: Histochem Cell Biol Subsets: MEDLINE
Imprint Name(s): Original Publication: Berlin : Springer
Ιατρικοί όροι (MeSH): Mitochondria*/metabolism , Induced Pluripotent Stem Cells*/metabolism , Induced Pluripotent Stem Cells*/cytology , Cellular Reprogramming*, Fibroblasts/metabolism ; Fibroblasts/cytology ; Reactive Oxygen Species/metabolism ; Humans ; Cells, Cultured ; Membrane Potential, Mitochondrial
Περίληψη: During the conversion of fibroblasts into induced pluripotent stem cells (iPSCs), cellular metabolism shifts from oxidative phosphorylation toward glycolysis; however, how functional and structural mitochondrial adaptations are coordinated remains incompletely understood. Here, we examined selected aspects of mitochondrial function, targeted gene expression, and ultrastructure in fibroblasts and iPSCs derived from healthy donors and patients with osteogenesis imperfecta (OI). Targeted gene expression analysis was performed in all four cell types, while functional and ultrastructural assays focused on OI-derived cells. Flow cytometry revealed reduced mitochondrial mass and reactive oxygen species (ROS) levels in iPSCs compared with fibroblasts. Mitochondrial membrane potential showed modestly reduced fluorescence depending on the probe used. Quantitative transmission electron microscopy demonstrated internal mitochondrial reorganization in iPSCs, including altered morphology and simplified cristae architecture, despite preservation of overall membrane integrity. These findings indicate that reprogramming induces coordinated functional downscaling and structural remodeling of mitochondria. Furthermore, differential expression of matrix metalloproteinases suggests that extracellular matrix remodeling accompanies metabolic adaptation during reprogramming.
(© 2026. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
Competing Interests: Declarations. Conflict of interest: The authors declare no competing interests.
References: Antioxidants (Basel). 2023 May 10;12(5):. (PMID: 37237941)
Cell Metab. 2011 Aug 3;14(2):264-71. (PMID: 21803296)
Stem Cells. 2024 Aug 1;42(8):706-719. (PMID: 38825983)
Exp Cell Res. 2019 Jun 1;379(1):55-64. (PMID: 30922922)
Int J Toxicol. 2020 May/Jun;39(3):241-247. (PMID: 32308077)
Ann N Y Acad Sci. 2015 Sep;1350:95-106. (PMID: 26335356)
Tissue Eng Regen Med. 2023 Aug;20(5):661-670. (PMID: 37160567)
Nucleic Acids Res. 2001 May 1;29(9):e45. (PMID: 11328886)
EMBO J. 2012 May 2;31(9):2103-16. (PMID: 22446391)
Trends Cell Biol. 2021 Apr;31(4):311-323. (PMID: 33422359)
Stem Cells. 2010 Apr;28(4):721-33. (PMID: 20201066)
Front Cell Dev Biol. 2024 Jan 11;11:1328522. (PMID: 38274274)
Development. 2017 Feb 15;144(4):541-551. (PMID: 28196802)
Stem Cells. 2010 Apr;28(4):661-73. (PMID: 20073085)
Cell Stress. 2019 May 27;3(6):181-194. (PMID: 31225513)
Genes Dis. 2020 Dec 23;8(6):891-906. (PMID: 34522716)
Circ Res. 2012 Feb 17;110(4):526-9. (PMID: 22343555)
PLoS One. 2011;6(11):e27352. (PMID: 22110631)
PLoS One. 2010 Nov 23;5(11):e14095. (PMID: 21124794)
Neurochem Int. 2018 Jul;117:65-76. (PMID: 28627365)
Front Bioeng Biotechnol. 2023 Jun 30;11:1205122. (PMID: 37456734)
Methods Protoc. 2025 Aug 06;8(4):. (PMID: 40863740)
Cell Metab. 2013 Sep 3;18(3):325-32. (PMID: 23850316)
Stem Cell Res Ther. 2016 Sep 09;7(1):129. (PMID: 27612636)
Int J Dev Biol. 2010;54(11-12):1729-41. (PMID: 21305470)
Cell Stem Cell. 2022 Dec 1;29(12):1703-1717.e7. (PMID: 36459970)
Gerontology. 2014;60(2):174-82. (PMID: 24281332)
Cell Metab. 2018 Feb 6;27(2):332-338. (PMID: 29414683)
Grant Information: PCN-2-034/N/2/O Institutional funding from Medical University of Silesia; BNW-1-154/N/3/1 Institutional funding from Medical University of Silesia
Contributed Indexing: Keywords: Cellular reprogramming; Induced pluripotent stem cells; Metabolic remodeling; Mitochondrial function; Mitochondrial ultrastructure; Transmission electron microscopy
Substance Nomenclature: 0 (Reactive Oxygen Species)
Entry Date(s): Date Created: 20260420 Date Completed: 20260715 Latest Revision: 20261010
Update Code: 20261010
DOI: 10.1007/s00418-026-02472-y
PMID: 42010006
Βάση Δεδομένων: MEDLINE
Περιγραφή
ISSN:1432-119X
DOI:10.1007/s00418-026-02472-y