| Literature DB >> 29938352 |
Emanuela Chiarella1, Annamaria Aloisio2, Bruna Codispoti3, Giovanna Nappo4, Stefania Scicchitano2, Valeria Lucchino2, Ylenia Montalcini2, Augusto Camarotti5, Olimpio Galasso6, Manfredi Greco7, Giorgio Gasparini6, Maria Mesuraca2, Heather Mandy Bond2, Giovanni Morrone2.
Abstract
Mesenchymal stem cells (MSCs) are multipotent progenitors present in the bone marrow stroma and in subcutaneous abdominal fat, an abundant and easily accessible source of MSCs with the ability to differentiate along multiple lineage pathways. The stem cell-associated transcription co-factor Zinc Finger Protein 521 (ZNF521/zfp521) has been implicated in the control of the homeostasis of hematopoietic, neural and osteo-adipogenic progenitors. Here we document through the analysis of a panel of human adipose-derived stem cells (hADSCs), that ZNF521 strongly inhibits the generation of mature adipocytes. Enforced overexpression of ZNF521 in these cells resulted in a significant delay and reduction in adipocyte differentiation upon exposure to inducers of adipogenesis. Of particular relevance, ZNF521 was able to inhibit the expression of ZNF423, recently identified as an essential commitment factor necessary for the generation of pre-adipocytes. Conversely, silencing of ZNF521 was found to significantly enhance the adipogenic differentiation of hADSCs. Inhibition of adipogenesis by ZNF521 was at least in part due to inhibition of EBF1. Taken together, these results confirm a role for ZNF521 as a key negative regulator of adipocyte differentiation of hADSCs.Entities:
Keywords: Adipogenesis; Gene expression; Gene transfer; Zinc finger protein 521 (ZNF521); human Adipose-Derived Stem Cells (hADSCs)
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Year: 2018 PMID: 29938352 DOI: 10.1007/s12015-018-9830-0
Source DB: PubMed Journal: Stem Cell Rev Rep ISSN: 2629-3277 Impact factor: 5.739