Cited by 31Mesenchymal stem cell researchLiver Disease and TransplantationHematopoietic Stem Cell Transplantation

Deficient Proliferation of Bone Marrow-Derived Mesenchymal Stem Cells in Patients with Chronic Hepatitis B Viral Infections and Cirrhosis of the Liver

Zhong, Yue-Si, Lin, Nan, Deng, Mei-Hai, Zhang, Fu-Cheng, Tang, Zhao-Feng, Xu, Rui-Yun·2010·Digestive Diseases and Sciences

Abstract

In this study, we determined whether the proliferation of bone marrow-derived mesenchymal stem cells (MSCs) is impaired in patients with chronic hepatitis B viral infection and cirrhosis of the liver. MSCs from 15 patients with chronic hepatitis B and cirrhosis of the liver (CIR-MSCs) and 11 normal donors (ND-MSCs) were collected and characterized in vitro. CIR-MSCs displayed an intact immunophenotype. The percentage of S-phase nuclei in CIR-MSCs (4.34%), however, was significantly lower than that in ND-MSCs (P < 0.001), indicating impaired proliferation of CIR-MSCs. Growth factor receptor expression (e.g., IGF1, PDGFalpha, and PDGFbeta) on the surface of CIR-MSCs decreased compared to that on ND-MSCs (P < 0.03). We found no evidence that CIR-MSCs were infected with the hepatitis B virus (HBV). Deficient proliferation of CIR-MSCs may result from the decreased expression of growth factor receptors and unbalanced production of cytokines in patients with HBV infection. Our results indicate that autologous MSCs of patients with chronic hepatitis B and cirrhosis of the liver may not be suitable for therapeutic purposes.

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Crossref · 10.1007/s10620-009-0733-4

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  • MSCs derived from older individuals or those with underlying health conditions, such as HBV infection, may exhibit impaired proliferative, differentiation, and regenerative capacities, leading to ineffective treatments or unfavorable clinical outcomes.

    “MSCs derived from older individuals or those with underlying health conditions, such as HBV infection, may exhibit impaired proliferative, differentiation, and regenerative capacities, leading to ineffective treatments or unfavorable clinical outcomes [315, 316].”

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Authors
Zhong, Y.-S., Lin, N., Deng, M.-H., Zhang, F.-C., Tang, Z.-F., & Xu, R.-Y.
Affiliations
Sun Yat-sen University (CN)
Venue
Digestive Diseases and Sciences
Published
2009-02-26
Volume
55
Issue
2
Pages
438-445
ISSN
  • 0163-2116 (ISSN-L)
  • 1573-2568
OpenAlex
W2003613883
Cited by
31
References
0
Citations by year
2025: 1 · 2023: 1 · 2022: 1 · 2021: 2 · 2020: 2 · 2019: 3 · 2018: 1 · 2017: 1 · 2016: 1 · 2015: 6 · 2014: 2 · 2013: 3 · 2012: 4
FWCI
1.10
Type
journal article
Language
en
Open access
closed
Locations
  • Digestive Diseases and Sciences (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Sun Yat-sen University
  • Science and Technology Development Fund
Topics
  • Health Sciences › Medicine › Genetics › Mesenchymal stem cell research
  • Health Sciences › Medicine › Hepatology › Liver Disease and Transplantation
  • Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
Keywords
mesenchymal stem cells, chronic hepatitis B, liver cirrhosis, cell proliferation, growth factor receptors, insulin-like growth factor I, platelet-derived growth factor, autologous stem cell therapy, hepatitis B
MeSH terms
Adult, Cells, Cultured, Female, Humans, Liver Cirrhosis, Male, Middle Aged, Severity of Illness Index, Receptors, Growth Factor, Disease Progression, Hepatitis B, Chronic, Cell Proliferation, Mesenchymal Stem Cells

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