乙醛脱氢酶基因ALDH2对雄性小鼠生育能力的影响
作者:
作者单位:

烟台大学生命科学学院 烟台 264003

作者简介:

徐文秀,女,硕士研究生;研究方向:细胞生物学;E-mail:xwx5935@163.com。

中图分类号:

Q492

基金项目:

国家重点研发计划项目(No. 2018YFC1003600);


The Effects of Acetaldehyde Dehydrogenase Gene ALDH2 on Male Mice Fertility
Author:
Affiliation:

School of Life Sciences, Yantai University, Yantai 264003, China

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    摘要:

    本研究使用乙醛脱氢酶2(ALDH2)基因全敲除的雄性C57BL/6(B6)小鼠(Mus musculus domesticus),通过分析不同周龄小鼠的睾丸脏器系数、睾丸组织细胞形态、精子运动参数、配种后母鼠产仔数及子代雄雌比等生育指标,探讨ALDH2基因敲除对雄性小鼠生育能力的影响。结果表明,与野生型(WT)小鼠相比,5、7、10周龄ALDH2基因敲除型(KO)雄性小鼠睾丸脏器系数显著降低(P < 0.05);睾丸组织细胞间质变大,精子活率显著降低(P < 0.05);产仔数和雄雌比显著降低(P < 0.05)。本研究为揭示乙醛脱氢酶ALDH2基因在雄性小鼠生殖中的作用提供了一定的基础。

    Abstract:

    [Objectives] The research on mammalian sexual reproduction is beneficial to the exploration of human reproduction mechanism, which focuses on reproductive system, germ cells, fertilization cells, external environmental factors, etc. There is little research on mammalian fertility after the elimination of metabolic enzymes from the body. It is known that aldehyde dehydrogenase 2 (ALDH2) is the most important enzyme for aldehyde oxidation, which can metabolize a large number of harmful aldehydes produced in the body. Studies have shown that a large number of reactive oxygen species produced by male sperm during exercise can increase the aldehyde content in sperm. Therefore, we studied the fertility of ALDH2 gene knockout male mice. [Methods] In this study, we analyze the testicular organ coefficient, testicular tissue cell morphology, sperm motility parameters, the number of offspring born after mating, and the ratio of male to female offspring of 52 male C57BL/6 mice of different weeks of age with ALDH2 gene knockout. Mean value comparison, one-way ANOVA, and t-test implemented in SPSS were used to explore the effect of ALDH2 gene knockout on fertility of male mice. [Results] We found that compared with the wild type (WT) mice, the weight and testicular organ coefficient of knockout (KO) mice at 5 and 10 weeks of age and mice at 3 and 10 weeks of age had extremely significant differences (n = 6, P < 0.01) (Table 1), the weight of mice at 3 and 7 weeks of age and testicular organ coefficient of mice at 5 and 7 weeks of age had significant differences (n = 6, P < 0.05) (Table 1). Among them, the cytoplasm of testicular tissue of 10 week old ALDH2 gene knockout male mice became larger (Fig. 2b); the sperm activity rate of knockout mice was significantly reduced (n = 6, P < 0.05) (Table 2); the litter size of ALDH2 transgenic mice was significantly reduced (6.7 ± 0.5) compared with wild type mice (11.0 ± 2.0, n = 3, P < 0.05), and the female to male ratio of ALDH2 gene knockout mice was also significantly reduced (0.8 ± 0.1 vs. 1.8 ± 0.5, n = 3, P < 0.05). [Conclusion] This study provides a basis for revealing the role of ALDH2 gene in male mouse reproduction and provides valuable information for the potential diagnosis and in vitro application of assisted reproductive technology.

    参考文献
    Chen C H, Ferreira J C, Gross E R, et al. 2014. Targeting aldehyde dehydrogenase 2:New therapeutic opportunities. Physiological Reviews, 94(1):1–34.
    Chen C H, Ferreira J C B, Mochly-Rosen D. 2019. ALDH2 and cardiovascular disease. Advances in Experimental Medicine and Biology, 1193(5):53–67.
    Chen C H, Sun L, Mochly-Rosen D. 2010. Mitochondrial aldehyde dehydrogenase and cardiac diseases. Cardiovascular Research, 88(1):51–57.
    Duan Y, Gao Y, Zhang J, et al. 2016. Mitochondrial aldehyde dehydrogenase 2 protects gastric mucosa cells against DNA damage caused by oxidative stress. Free Radical Biology and Medicine, 93(4):165–176.
    Ebert A D, Kodo K, Liang P, et al. 2014. Characterization of the molecular mechanisms underlying increased ischemic damage in the aldehyde dehydrogenase 2 genetic polymorphism using a human induced pluripotent stem cell model system. Science Translational Medicine, 6(255):255–130.
    Gibb Z, Lambourne S R, Curry B J, et al. 2016. Aldehyde dehydrogenase plays a pivotal role in the maintenance of stallion sperm motility. Biology of Reproduction, 94(6):133.
    Hu X Y, Fang Q, Wang J S, et al. 2011. Over-expression of aldehyde ehydrogenase-2 protects against H2O2-induced oxidative damage and apoptosis in peripheral blood mononuclear cells. Acta Pharmacologica Sinica, 32(2) :245–252.
    Inoue N, Wada I. 2018. Monitoring dimeric status of IZUMO1 during the acrosome reaction in living spermatozoon. Cell Cycle, 17(11):1279–1285.
    Li S Y, Li Q, Shen J J, et al. 2006. Attenuation of acetaldehyde- induced cell injury by overexpression of aldehyde dehydrogenase-2 (ALDH2) transgene in human cardiac myocytes:role of MAP kinase signaling. Journal of Molecular and Cellular Cardiology, 40(2):283–294.
    Liu X, Sun X, Liao H, et al. 2015. Mitochondrial aldehyde dehydrogenase 2 regulates revascularization in chronic ischemia:potential impact on the development of coronary collateral circulation. Arteriosclerosis, Thrombosis, and Vascular Biology, 35(10):2196–2206.
    Ma C, Yu B, Zhang W, et al. 2017. Associations between aldehyde dehydrogenase 2 (ALDH2) rs671 genetic polymorphisms, lifestyles and hypertension risk in Chinese Han people. Bioscience Reports, 7(1):11136.
    Ren J, Sowers J R, Zhang Y. 2018. Metabolic stress, autophagy, and cardiovascular aging:from pathophysiology to therapeutics. Trology and Metabolism, 29(10):699–711.
    Sinclair D. 2006. Deleterious pleiotropic effects of the atypical aldehyde dehydrogenase 2 (ALDH2) allele:comment on Luo. Biochemical Genetics, 44(7/8):385–390.
    Wang L S, Wu Z X. 2019. ALDH2 and cancer therapy. Advances in Experimental Medicine and Biology, 1193(8):221–228.
    Wei S, Zhang L, Bailu W, et al. 2019. ALDH2 deficiency inhibits Ox- LDL induced foam cell formation via suppressing CD36 expression. Biochemical and Biophysical Research Communications, 512(1):41–48.
    Weng Z, Ohtani K, Suda M, et al. 2014. Assessment of the reproductive toxicity of inhalation exposure to ethyl tertiary butyl ether in male mice with normal, low active and inactive ALDH2. Archives of Toxicology, 88(4):1007–1021.
    Wu N, Ren J. 2019. Aldehyde dehydrogenase 2 (ALDH2) and aging:Is there a sensible link? Advances in Experimental Medicine and Biology, 1193(8):237–253.
    Xu F, Chen Y, Lv R, et al. 2010. ALDH2 genetic polymorphism and the risk of type II diabetes mellitus in CAD patients. Hypertension Research, 33(1):49–55.
    Yamauchi M, Takeda K, Sakamoto K, et al. 2001. Association of polymorphism in the alcohol dehydrogenase 2 gene with alcohol-induced testicular atrophy. Alcoholism-Clinical and Experimental Research, 25(6):16–8.
    Yang K, Ren J, Li X, et al. 2020. Prevention of aortic dissection and aneurysm via an ALDH2-mediated switch in vascular smooth muscle cell phenotype. European Heart Journal, 41(26):2442– 2453.
    Yoval-Sanchez B, Rodriguez-Zavala J S. 2012. Differences in susceptibility to inactivation of human aldehyde dehydrogenases by lipid peroxidation byproducts. Chemical Research in Toxicology, 25(3):722–729.
    Yu H S, Oyama T, Isse T, et al. 2009. Characteristics of aldehyde dehydrogenase 2 (Aldh2) knockout mice. Toxicology Mechanisms and Methodst, 19(9):535–540.
    Zhu Z Y, Liu Y D, Gong Y, et al. 2022. Mitochondrial aldehyde dehydrogenase (ALDH2) rescues cardiac contractile dysfunction in an APP/PS1 murine model of Alzheimer’s disease via inhibition of ACSL4-dependent ferroptosis. Acta Pharmacologica Sinica, 43(1):39–49.
    田洪成, 马良宏, 马会明, 等. 2016. 单次热应激对小鼠睾丸雄激素受体的影响. 宁夏医学杂志, 38(4):289–290.
    王洪巨, 康品方, 叶红伟, 等. 2012. 乙醛脱氢酶2在糖尿病大鼠心肌缺血/再灌注损伤中的抗凋亡作用. 南方医科大学学报, 32(3):345–348.
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徐文秀,刘庆玲,刘笑含,孔令英,董思林,许文达,石慧,赵振军.2023.乙醛脱氢酶基因ALDH2对雄性小鼠生育能力的影响.动物学杂志,58(4):590-596.

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  • 收稿日期:2022-09-19
  • 在线发布日期: 2023-08-18