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The Protective Role of Autophagy in Heterocephalus glaber Hepatic Stellate Cells Exposed to H2O2 or Nutritional Stress

Authors :
Shanmin Zhao
Hong Luo
Guanghan Kan
Yong Zhao
Lifang Lin
Qiu Tang
Chenlin Yu
Wei Sun
Liping Cai
Shufang Cui
Source :
Cellular Physiology and Biochemistry, Vol 34, Iss 2, Pp 463-473 (2014)
Publication Year :
2014
Publisher :
Cell Physiol Biochem Press GmbH & Co KG, 2014.

Abstract

Background/Aims: Naked mole rats (NMRs) survive and thrive in dark, dank environments with low levels of oxygen and poor quality nutrition. Their long lifespan is attributed to sustained good health and pronounced resistance to cancer. Physiological and biochemical processes, such as autophagy, may contribute to the successful aging of this exceptionally long-lived species. We demonstrated that NMRs have higher levels of autophagy than short-lived C57BL/6 mice, and this may play an important role in the maintenance of cellular protein quality and the defense of cells against intracellular and extracellular aggressors in NMRs. The present study assesses autophagy as a means for cells to flexibly respond to environmental changes (H2O2 treatment and a shortage of nutrients). Methods: Primary NMR HSCs were isolated from liver and treated with serum-free medium. Cells in the experimental group were incubated with different concentrations of hydrogen peroxide (H2O2) in the presence and / or absence of 3-MA (5 mM).The LC3-II/LC3-I ratio was determined by western blot analysis. Western blotting was performed to analyze the expression level of Beclin 1 protein. Apoptosis and cell-cycle progression were analyzed by flow cytometry. Results: Our data reveal that both poor quality nutrition and H2O2 treatment induces apoptosis and autophagy in NMR hepatic stellate cells(HSCs). Conclusion: NMR cells have the capacity to induce cell death through apoptosis and downregulate the energy consuming processes through inhibition of proliferation when they become superfluous or irreversibly damaged.

Details

Language :
English
ISSN :
10158987 and 14219778
Volume :
34
Issue :
2
Database :
Directory of Open Access Journals
Journal :
Cellular Physiology and Biochemistry
Publication Type :
Academic Journal
Accession number :
edsdoj.8bb4690557344f29985deb8b9ae7be9
Document Type :
article
Full Text :
https://doi.org/10.1159/000363015