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Published on: June 15, 2018
[Effect and related mechanism of miRNA-21 on hydrogen peroxide-induced C-kit(+) cardiac stem cells apoptosis]
1Department of Cardiology, Affiliated Hospital of Zunyi Medical College, Zunyi 563000, China.
Abstract:
Objective: To explored the effect and related mechanism of miRNA-21 on hydrogen peroxide-induced C-kit(+) cardiac stem cells apoptosis. Methods: C-kit(+) cardiac stem cells were isolated from SD rats by the methods of enzyme digestion and magnetic bead. Cells were divided into the following experimental groups: (1) negative control mimics (NCM)group: cells were transfected with negative control miRNA-21 mimics for 48 hours; (2)mimics group: cells were transfected with miRNA-21 mimics for 48 hours; (3) NCM+ H(2)O(2) group: negative control miRNA-21 mimics were transfected into cells for 48 hours and then treated with 100 μmol H(2)O(2) for 2 hours; (4)mimics+ H(2)O(2) group: miRNA-21 mimics were transfected into cells for 48 hours and then treated with 100 μmol H(2)O(2) for 2 hours. mRNA of miRNA-21 was detected by RT-PCR. The apoptosis rate of C-kit(+) cardiac stem cells was determined using the annexin V-FITC/PI staining assay. Western blot was employed to measure the expression of apoptosis related proteins(Caspase-3, Bax, and Bcl-2). Results: (1) Compared with the NCM group, the mRNA expression level of miRNA-21 was significantly up-regulated in mimics group, while obviously down-regulated in NCM+ H(2)O(2) group(all P<0.05). Compared with the mimics group, the mRNA expression levels of miRNA-21 in mimics+ H(2)O(2) group was significantly downregulated (P<0.05), but remarkably upregulated compared with the NCM+ H(2)O(2) group(P<0.05). (2) Flow cytometry results indicated that the early apoptosis rates were similar between the NCM group and mimics group ((4.57±3.45)% vs. (5.13±3.21)%, P>0.05). Compared with the NCM group, the early apoptosis rates were remarkably increased ((79.07±5.75)% vs.(4.57±3.45)%, P<0.05) in NCM+ H(2)O(2) group. Compared with the mimics group, the early apoptosis was significantly up-regulated in the mimics+ H(2)O(2) group ((30.27±1.36)% vs.(5.13±3.21)%, P<0.05), which were further down-regulated in mimics+ H(2)O(2) group compared with the NCM+ H(2)O(2) group ((30.27±1.36)% vs.(79.07±5.75)%, P<0.05). (3) Western blot results showed similar protein expression of Caspase-3, Bax and Bcl-2 between NCM group and mimics group(all P>0.05). Compared with the NCM group, the Caspase-3 and Bax protein expression was significantly increased in NCM+ H(2)O(2) group (all P<0.05), but the protein expression level of Bcl-2 was similar between the 2 groups(P>0.05). The Caspase-3 and Bax protein expression was markedly decreased, while Bcl-2 apparently increased in the mimics+ H(2)O(2) group compared with the NCM+ H(2)O(2) group(all P<0.05). Conclusion: Overexpression of miRNA-21 protects the C-kit(+) cardiac stem cells from apoptosis caused by oxidative stress through downregulating proapoptotic and upregulating the antiapoptotic proteins.
Insights
MicroRNA-21 (miRNA-21) overexpression protects cardiac stem cells from hydrogen peroxide-induced apoptosis. This protection involves downregulating pro-apoptotic proteins and upregulating anti-apoptotic proteins, offering a potential therapeutic mechanism for oxidative stress in the heart.
Area of Science:
- Cardiovascular Biology
- Stem Cell Research
- Molecular Biology
Background:
- Oxidative stress contributes to cardiac dysfunction and stem cell apoptosis.
- MicroRNAs play crucial roles in regulating cellular processes, including apoptosis.
- C-kit(+) cardiac stem cells are vital for cardiac repair.
Purpose of the Study:
- To investigate the effect of microRNA-21 on hydrogen peroxide-induced apoptosis in C-kit(+) cardiac stem cells.
- To elucidate the underlying molecular mechanisms of miRNA-21's protective role.
Main Methods:
- Isolation and culture of C-kit(+) cardiac stem cells from SD rats.
- Transfection with miRNA-21 mimics or negative control mimics.
- Induction of oxidative stress using hydrogen peroxide (H2O2).
- Assessment of apoptosis rates via flow cytometry (Annexin V-FITC/PI staining).
- Measurement of apoptosis-related protein expression (Caspase-3, Bax, Bcl-2) using Western blot.
Main Results:
- miRNA-21 expression was modulated by transfection and H2O2 treatment.
- H2O2 significantly increased apoptosis rates in cardiac stem cells.
- Overexpression of miRNA-21 markedly reduced H2O2-induced apoptosis.
- miRNA-21 overexpression downregulated pro-apoptotic proteins (Caspase-3, Bax) and upregulated anti-apoptotic protein (Bcl-2).
Conclusions:
- MicroRNA-21 overexpression confers significant protection to C-kit(+) cardiac stem cells against oxidative stress-induced apoptosis.
- The protective mechanism involves the modulation of key apoptosis-regulating proteins.
- miRNA-21 represents a potential therapeutic target for mitigating cardiac damage from oxidative stress.

