Your browser doesn't support javascript.
loading
Human gingival mesenchymal stem cells-lyosecretome attenuates adverse effect of hydrogen peroxide-induced oxidative stress on osteoblast cells.
Kusumawardani, Banun; Nurul Amin, Muhammad; Rahayu, Yani C; Sari, Desi S; Altariq, Morin I; Putri, Arini H; Kanya, Amara; Prahasanti, Chiquita; Aljunaid, Mohammed A.
Afiliação
  • Kusumawardani B; Department of Biomedical Sciences, Faculty of Dentistry, University of Jember, Indonesia.
  • Nurul Amin M; Department of Biomedical Sciences, Faculty of Dentistry, University of Jember, Indonesia.
  • Rahayu YC; Department of Oral Biology, Faculty of Dentistry, University of Jember, Indonesia.
  • Sari DS; Department of Periodontics, Faculty of Dentistry, University of Jember, Indonesia.
  • Altariq MI; Undergraduate Program of Dental Medicine, Faculty of Dentistry, University of Jember, Indonesia.
  • Putri AH; Undergraduate Program of Dental Medicine, Faculty of Dentistry, University of Jember, Indonesia.
  • Kanya A; Undergraduate Program of Dental Medicine, Faculty of Dentistry, University of Jember, Indonesia.
  • Prahasanti C; Department of Periodontics, Faculty of Dental Medicine, Airlangga University, Indonesia.
  • Aljunaid MA; Doctoral Program of Dental Medicine, Faculty of Dental Medicine, Airlangga University, Surabaya, Indonesia.
J Taibah Univ Med Sci ; 19(3): 687-695, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38831997
ABSTRACT

Objective:

To determine total protein content, antioxidant activity, and protective ability of lyophilized human gingival mesenchymal stem cells (hGMSCs)-secretome in hydrogen peroxide (H2O2) induced oxidative stress model.

Methods:

Human GMSCs were cultured to obtain a conditioned medium (secretome), then lyophilized to produce lyosecretome. Total protein was determined by bicinchoninic acid assay (BCA) and SDS-PAGE to improve protein measurements. Antioxidant concentration was measured by ABTS assay, while the protective ability of lyosecretome against oxidative stress was determined by the metabolic activity of osteoblast cells. The study group was divided into a control group (culture medium) and a lyosecretome treatment group (0.0; 0.157, 0.313, 0.625, 1.25, 2.5, 5, and 10 mg/mL + H2O2).

Results:

Lyosecretome had a protein concentration of 2086.00 ± 0.20 µg/ml, with a molecular weight of 174, 74, 61, 55, and 26 kDa, which are thought to facilitate cell migration, as well as bind cytokines and growth factors. Lyosecretome also provided the highest antioxidant activity of 93.51% at a concentration of 4.8 mg/ml, with an IC50 value of 2.08 mg/ml. The highest cell metabolic activity (79.53 ± 2.41%) was shown in the 1.25 mg/ml lyosecretome treatment group. All concentrations of hGMSC-lyosecretome attenuate the adverse effect of H2O2-induced oxidative stress.

Conclusion:

Lyosecretome obtained from hGMSCs can maintain metabolic activity in osteoblast cells as protection against H2O2 oxidative stress.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article