Bone Marrow-Derived Mesenchymal Stem Cells Isolated from Patients with Cirrhosis and Healthy Volunteers Show Comparable Characteristics

Yoo Li Lim, Young Woo Eom, Su Jung Park, Taeui Hong, Seong Hee Kang, Soon Koo Baik, Kyu Sang Park, Moon Young Kim

Research output: Contribution to journalArticlepeer-review

Abstract

Background and Objectives: Autologous or allogeneic bone marrow-derived mesenchymal stem cells (BMSCs) have been applied in clinical trials to treat liver disease. However, only a few studies are comparing the characteristics of autologous MSCs from patients and allogeneic MSCs from normal subjects. Methods and Results: We compared the characteristics of BMSCs (BCs and BPs, respectively) isolated from six healthy volunteers and six patients with cirrhosis. In passage 3 (P3), senescent population and expression of p53 and p21 were slightly higher in BPs, but the average population doubling time for P3–P5 in BPs was approximately 65.3±11.1 h, which is 18.4 h shorter than that in BCs (83.7±9.2 h). No difference was observed in the expression of CD73, CD90, or CD105 between BCs and BPs. Adipogenic differentiation slightly increased in BCs, but the expression levels of leptin, peroxisome proliferator-activated receptor γ, and CCAAT-enhancer-binding protein α did not vary between differentiated BCs and BPs. While ATP and reactive oxygen species levels were slightly lower in BPs, mitochondrial membrane potential, oxygen consumption rate, and expression of mitochondria-related genes such as cytochrome c oxidase 1 were not significantly different between BCs and BPs. Conclusions: Taken together, there are marginal differences in the proliferation, differentiation, and mitochondrial activities of BCs and BPs, but both BMSCs from patients with cirrhosis and healthy volunteers show comparable characteristics.

Original languageEnglish
Pages (from-to)394-403
Number of pages10
JournalInternational Journal of Stem Cells
Volume13
Issue number3
DOIs
Publication statusPublished - 2020 Nov

Bibliographical note

Funding Information:
This work was supported by a grant from the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (HI17C1365), funded by the Ministry of Health & Welfare, Republic of Korea, and a Basic Science Research Program through the National Research Foundation of Korea (2017R1D1A1A 02019212 and 2018R1C1B5044890), funded by the Korean government, the Ministry of Education and the Medical Research Center Program (2017R1A5A2015369) from the Ministry of Science and ICT.

All Science Journal Classification (ASJC) codes

  • Developmental Biology
  • Cell Biology

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