Human gingival mesenchymal stem cells retain their growth and immunomodulatory characteristics independent of donor age

Author:

Dave Jay R.1ORCID,Chandekar Sayali S.1,Behera Shubhanath2ORCID,Desai Kaushik U.1ORCID,Salve Pradnya M.1,Sapkal Neha B.1,Mhaske Suhas T.1,Dewle Ankush M.1,Pokare Parag S.1,Page Megha3,Jog Ajay3,Chivte Pankaj A.4,Srivastava Rupesh K.5ORCID,Tomar Geetanjali B.1ORCID

Affiliation:

1. Institute of Bioinformatics and Biotechnology, Savitribai Phule Pune University, Pune, 411007 Maharashtra, India.

2. National Centre for Cell Science, Savitribai Phule Pune University Campus, Pune, 411007 Maharashtra, India.

3. Department of Dentistry, Deenanath Mangeshkar Hospital and Research Centre, Pune, 411004 Maharashtra, India.

4. Saraswati Danwantri Dental College and Hospital, Parbhani, 431401 Maharashtra, India.

5. Department of Biotechnology, All India Institute of Medical Science, New Delhi 110029, India.

Abstract

Aging has been reported to deteriorate the quantity and quality of mesenchymal stem cells (MSCs), which affect their therapeutic use in regenerative medicine. A dearth of age-related stem cell research further restricts their clinical applications. The present study explores the possibility of using MSCs derived from human gingival tissues (GMSCs) for studying their ex vivo growth characteristics and differentiation potential with respect to donor age. GMSCs displayed decreased in vitro adipogenesis and in vitro and in vivo osteogenesis with age, but in vitro neurogenesis remained unaffected. An increased expression of p53 and SIRT1 with donor age was correlated to their ability of eliminating tumorigenic events through apoptosis or autophagy, respectively. Irrespective of donor age, GMSCs displayed effective immunoregulation and regenerative potential in a mouse model of LPS-induced acute lung injury. Thus, we suggest the potential of GMSCs for designing cell-based immunomodulatory therapeutic approaches and their further extrapolation for acute inflammatory conditions such as acute respiratory distress syndrome and COVID-19.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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