Scrima 2022 Stem Cell Res Ther

From Bioblast
Publications in the MiPMap
Scrima R, Agriesti F, Pacelli C, Piccoli C, Pucci P, Amoresano A, Cela O, Nappi L, Tataranni T, Mori G, Formisano P, Capitanio N (2022) Myoglobin expression by alternative transcript in different mesenchymal stem cells compartments.

Β» Stem Cell Res Ther 13:209. PMID: 35598009 Open Access

Scrima Rosella,  Agriesti Francesca,  Pacelli Consiglia,  Piccoli Claudia,  Pucci Pietro,  Amoresano Angela,  Cela Olga, Nappi Luigi,  Tataranni Tiziana,  Mori Giorgio,  Formisano Pietro,  Capitanio Nazzareno (2022) Stem Cell Res Ther

Abstract: The metabolic phenotype of stem cells is increasingly recognized as a hallmark of their pluripotency with mitochondrial and oxygen-related metabolism playing a not completely defined role in this context. In a previous study, we reported the ectopic expression of myoglobin (MB) in bone marrow-derived hematopoietic stem/progenitor cells. Here, we have extended the analysis to mesenchymal stem cells (MSCs) isolated from different tissues.

MSCs were isolated from human placental membrane, mammary adipose tissue and dental pulp and subjected to RT-PCR, Western blotting and mass spectrometry to investigate the expression of MB. A combination of metabolic flux analysis and cyto-imaging was used to profile the metabolic phenotype and the mitochondria dynamics in the different MSCs.

As for the hematopoietic stem/progenitor cells, the expression of Mb was largely driven by an alternative transcript with the protein occurring both in the monomer and in the dimer forms as confirmed by mass spectrometry analysis. Comparing the metabolic fluxes between neonatal placental membrane-derived and adult mammary adipose tissue-derived MSCs, we showed a significantly more active bioenergetics profile in the former that correlated with a larger co-localization of myoglobin with the mitochondrial compartment. Differences in the structure of the mitochondrial network as well as in the expression of factors controlling the organelle dynamics were also observed between neonatal and adult mesenchymal stem cells. Finally, the expression of myoglobin was found to be strongly reduced following osteogenic differentiation of dental pulp-derived MSCs, while it was upregulated following reprogramming of human fibroblasts to induce pluripotent stem cells.

Ectopic expression of myoglobin in tissues other than muscle raises the question of understanding its function therein. Properties in addition to the canonical oxygen storage/delivery have been uncovered. Finding of Mb expressed via an alternative gene transcript in the context of different stem cells with metabolic phenotypes, its loss during differentiation and recovery in iPSCs suggest a hitherto unappreciated role of Mb in controlling the balance between aerobic metabolism and pluripotency. Understanding how Mb contributes through modulation of the mitochondrial physiology to the stem cell biology paves the way to novel perspectives in regenerative medicine as well as in cancer stem cell therapy. β€’ Keywords: Bioenergetics, Cyto-imaging, Mass spectrometry, Mesenchymal stem cells, Metabolic flux analysis, Mitochondria, Myoglobin β€’ Bioblast editor: Plangger M β€’ O2k-Network Lab: IT Foggia Capitanio N

Labels: MiParea: Respiration 

Organism: Human  Tissue;cell: Stem cells  Preparation: Intact cells 

Coupling state: ROUTINE  Pathway: ROX  HRR: Oxygraph-2k 


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