Novel Immortalized Human Multipotent Mesenchymal Stromal Cell Line for Studying Hormonal Signaling

Author:

Primak Alexandra1ORCID,Kalinina Natalia1,Skryabina Mariya1,Usachev Vladimir1,Chechekhin Vadim1,Vigovskiy Maksim1ORCID,Chechekhina Elizaveta1,Voloshin Nikita1,Kulebyakin Konstantin12ORCID,Kulebyakina Maria12ORCID,Grigorieva Olga12,Tyurin-Kuzmin Pyotr1ORCID,Basalova Nataliya12ORCID,Efimenko Anastasia12ORCID,Dzhauari Stalik1,Antropova Yulia1,Plyushchii Ivan1,Akopyan Zhanna12ORCID,Sysoeva Veronika1ORCID,Tkachuk Vsevolod12,Karagyaur Maxim12

Affiliation:

1. Faculty of Medicine, Lomonosov Moscow State University, 119234 Moscow, Russia

2. Institute for Regenerative Medicine, Medical Research and Education Center, Lomonosov Moscow State University, 119234 Moscow, Russia

Abstract

Multipotent mesenchymal stromal cells (MSCs) integrate hormone and neuromediator signaling to coordinate tissue homeostasis, tissue renewal and regeneration. To facilitate the investigation of MSC biology, stable immortalized cell lines are created (e.g., commercially available ASC52telo). However, the ASC52telo cell line has an impaired adipogenic ability and a depressed response to hormones, including 5-HT, GABA, glutamate, noradrenaline, PTH and insulin compared to primary cells. This markedly reduces the potential of the ASC52telo cell line in studying the mechanisms of hormonal control of MSC’s physiology. Here, we have established a novel immortalized culture of adipose tissue-derived MSCs via forced telomerase expression after lentiviral transduction. These immortalized cell cultures demonstrate high proliferative potential (up to 40 passages), delayed senescence, as well as preserved primary culture-like functional activity (sensitivity to hormones, ability to hormonal sensitization and differentiation) and immunophenotype up to 17–26 passages. Meanwhile, primary adipose tissue-derived MSCs usually irreversibly lose their properties by 8–10 passages. Observed characteristics of reported immortalized human MSC cultures make them a feasible model for studying molecular mechanisms, which regulate the functional activities of these cells, especially when primary cultures or commercially available cell lines are not appropriate.

Funder

Russian Science Foundation

Publisher

MDPI AG

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