miR-191靶向BDNF基因通过激活PI3K/AKT信号通路促进猪未成熟支持细胞增殖
收稿日期: 2021-04-25
修回日期: 2021-06-02
网络出版日期: 2021-06-11
基金资助
湖南省自然科学基金项目编号(2020JJ4348);湖南省重点研发计划项目项目编号(2020NK2024);湖南省生猪产业技术体系岗位专家项目资助
MiR-191 promotes the porcine immature Sertoli cell proliferation by targeting the BDNF gene through activating the PI3K/AKT signaling pathway
Received date: 2021-04-25
Revised date: 2021-06-02
Online published: 2021-06-11
Supported by
Supported by the Natural Science Foundation of Hunan Province No(2020JJ4348);the Key Research and Development Plan Projects of Hunan ProvinceNo(2020NK2024);the Project from Porcine Industry and Technology System of Hunan Province
睾丸支持细胞数量是影响精子生成能力的主要因素之一,microRNA (miRNA)参与调控猪未成熟支持细胞的发育过程,然而,大多数被鉴定出的miRNA对支持细胞的作用及其机制尚不明确。基于本课题组前期高内涵筛选结果,本文进一步通过流式细胞术、蛋白免疫印迹和双荧光素酶报告基因等方法,研究了miR-191调控猪未成熟支持细胞增殖和凋亡的作用机理。结果表明:过表达miR-191显著促进细胞周期由G1期进入S期和G2期,细胞增殖能力显著增强,细胞凋亡率显著降低;而抑制表达miR-191则与之相反。双荧光素酶报告基因系统验证miR-191直接靶向BDNF基因3′-UTR。抑制表达BDNF基因促进细胞周期进入S期,并促进细胞增殖而抑制细胞凋亡,与过表达miR-191的作用一致。共转染试验结果显示,BDNF基因可以拮抗miR-191对细胞增殖和凋亡的调控作用。此外,过表达miR-191和抑制表达BDNF基因均可显著促进PI3K/AKT信号通路中关键蛋白PI3K和AKT的磷酸化水平,且BDNF基因同样拮抗miR-191对PI3K和AKT蛋白的调控作用。本研究结果证实miR-191靶向BDNF基因,通过激活PI3K/AKT信号通路促进猪未成熟支持细胞增殖且抑制其凋亡,为进一步解析miR-191调控猪精子生成的生物学功能提供了理论基础。
关键词: miR-191; BDNF基因; PI3K/AKT信号通路; 增殖; 猪睾丸支持细胞
唐湘薇, 楚丹, 颜赛娜, 尹艳飞, 卞桥, 翁波, 陈斌, 冉茂良 . miR-191靶向BDNF基因通过激活PI3K/AKT信号通路促进猪未成熟支持细胞增殖[J]. 遗传, 2021 , 43(7) : 680 -693 . DOI: 10.16288/j.yczz.21-154
The number of Sertoli cells in the testis is a major regulator on the sperm production capacity. MicroRNAs (miRNAs) participate in regulating the proliferation and apoptosis of porcine immature Sertoli cells. However, the functions and mechanisms of action of most identified miRNAs in porcine Sertoli cells remain largely unknown. In the present study, based on our previous results from an EdU-based high-content screening assay, we further studied the mechanism of action of miR-191 on the proliferation and apoptosis of porcine immature Sertoli cells through flow cytometry, Western blotting, and dual-luciferase activity analyses. The results demonstrated that overexpression of miR-191 promoted cell cycle progression from G1 phase to the S and G2 phases, enhanced cell proliferation, and inhibited apoptosis in the porcine immature Sertoli cells, whereasmiR-191 inhibition resulted in the opposite effects. The results from a luciferase reporter assay showed that miR-191 directly targeted the 3′-UTR of theBDNF gene. BDNF knockdown also promoted cell cycle progression to the S phase, cell proliferation and inhibited cell apoptosis, which were consistent with the effects of the miR-191overexpression. A co-transfection experiment showed that BDNF knockdown abolished the effects of miR-191 inhibition. Furthermore, both miR-191 overexpression and BDNFinhibition elevated the phosphorylation of PI3K and AKT, the key components of the PI3K/AKT signaling pathway, whereas BDNFinhibition offset the effects of the miR-191 knockdown. Overall, these data indicated that miR-191 promotes cell proliferation and inhibits apoptosis in porcine immature Sertoli cells by targeting theBDNF gene through activating the PI3K/AKT signaling pathway. This study provides a novel scientific basis for further investigation on the biological functions of miR-191 on porcine spermatogenesis.
Key words: miR-191; BDNF gene; PI3K/AKT signaling pathway; proliferation; porcine Sertoli cells
| [1] | Franca LR, Hess RA, Dufour JM, Hofmann MC, Griswold MD. The Sertoli cell: one hundred fifty years of beauty and plasticity. Andrology, 2016, 4(2):189-212. |
| [2] | Rebourcet D, Darbey A, Monteiro A, Soffientini U, Tsai YT, Handel I, Pitetti JL, Nef S, Smith LB, O'Shaughnessy PJ. Sertoli cell number defines and predicts germ and leydig cell population sizes in the adult mouse testis. Endocrinology, 2017, 158(9):2955-2969. |
| [3] | Bertoldo MJ, Guibert E, Faure M, Guillou F, RaméC, Nadal-Desbarats L, Foretz M, Viollet B, Dupont J, Froment P. Specific deletion of AMP-activated protein kinase (α1AMPK) in mouse Sertoli cells modifies germ cell quality. Mol Cell Endocrinol, 2016, 423:96-112. |
| [4] | Ran ML, Chen B, Wu MS, Liu XC, He CQ, Yang AQ, Li Z, Xiang YJ, Li ZH, Zhang SW. Integrated analysis of miRNA and mRNA expression profiles in development of porcine testes. Rsc Adv, 2015, 5(78):63439-63449. |
| [5] | Ding HS, Liu M, Zhou CF, You XB, Su T, Yang YB, Xu DQ. Integrated analysis of miRNA and mRNA expression profiles in testes of Duroc and Meishan boars. BMC Genomics, 2020, 21(1):686. |
| [6] | Luo ZY, Dai XL, Ran XQ, Cen YX, Niu X, Li S, Huang SH, Wang JF. Identification and profile of microRNAs in Xiang pig testes in four different ages detected by Solexa sequencing. Theriogenology, 2018, 117:61-71. |
| [7] | Chen XX, Zheng Y, Li XL, Gao Q, Feng TY, Zhang PF, Liao MZ, Tian XE, Lu HZ, Zeng WX. Profiling of miRNAs in porcine Sertoli cells. J Anim Sci Biotechnol, 2020, 11:85. |
| [8] | Ma CP, Song HB, Yu L, Guan KF, Hu PD, Li Y, Xia XY, Li JL, Jiang SW, Li FG. miR-762 promotes porcine immature Sertoli cell growth via the ring finger protein 4 (RNF4) gene. Sci Rep, 2016, 6:32783. |
| [9] | Zhang SX, Guo J, Liang MD, Qi JJ, Wang ZB, Jian XR, Zhang ZB, Sun BX, Li ZH. miR-196a promotes proliferation and inhibits apoptosis of immature porcine Sertoli cells. DNA Cell Biol, 2019, 38(1):41-48. |
| [10] | Gao H, Ran ML, Luo H, Weng B, Tang XW, Chen Y, Yang AQ, Chen B. miR-499 promotes immature porcine Sertoli cell growth by the PI3K/AKT pathway by targeting the PTEN gene. Reproduction, 2019, 152(2):145-157. |
| [11] | Hu Y, Deng J, Tian K, Yang WR, Luo NJ, Lian Y, Gan L, Tang XY, Luo HY, Zhang JJ, Wang XZ. MiR-8-3p regulates hyperthermia-induced lactate secretion by targeting PPP2R5B in boar Sertoli cells. Mol Reprod Dev, 2019, 86(11):1720-1730. |
| [12] | Guo J, Yang C, Zhang SX, Liang MD, Qi JJ, Wang ZB, Peng YH, Sun BX. MiR-375 induces ROS and apoptosis in ST cells by targeting the HIGD1A gene. Gene, 2019, 685:136-142. |
| [13] | Zhang JJ, Wang Y, Yang WR, Kee JD, Wang XZ. MicroRNA-1285 regulates 17β-estradiol-inhibited immature boar Sertoli cell proliferation via adenosine monophosphate-activated protein kinase activation. Endocrinology, 2015, 156(11):4059-4070. |
| [14] | Ran M, Li Z, Cao R, Weng B, Peng F, He C, Chen B. miR-26a suppresses autophagy in swine Sertoli cells by targeting ULK2. Reprod Domest Anim, 2018, 53(4):864-871. |
| [15] | Luo H, Chen B, Weng B, Tang XW, Chen Y, Yang AQ, Chu D, Zeng XY, Ran ML. miR-130a promotes immature porcine Sertoli cell growth by activating SMAD5 through the TGF-β-PI3K/AKT signaling pathway. FASEB J, 2020, 34(11):15164-15179. |
| [16] | Tian F, Yu CT, Wu M, Wu XY, Wan LF, Zhu XJ. MicroRNA-191 promotes hepatocellular carcinoma cell proliferation by has_circ_0000204/miR-191/KLF6 axis. Cell Prolif, 2019, 52(5):e12635. |
| [17] | Gao XT, Xie ZQ, Wang ZG, Cheng KL, Liang K, Song ZQ. Overexpression of miR-191 predicts poor prognosis and promotes proliferation and invasion in esophageal squamous cell carcinoma. Yonsei Med J, 2017, 58(6):1101-1110. |
| [18] | Polioudakis D, Abell NS, Iyer VR. MiR-191 regulates primary human fibroblast proliferation and directly targets multiple oncogenes. PLoS One, 2015, 10(5):e0126535. |
| [19] | Ma CP, Song HB, Guan KF, Zhou JW, Xia XY, Li FG. Characterization of swine testicular cell line as immature porcine Sertoli cell line. In Vitro Cell Dev Biol Anim, 2016, 52(4):427-433. |
| [20] | Ni FD, Hao SL, Yang WX. Multiple signaling pathways in Sertoli cells: recent findings in spermatogenesis. Cell Death Dis, 2019, 10(8):541. |
| [21] | Berger T, Nitta-Oda BJ. Sertoli cell proliferation in juvenile boars and microRNA. Livest Sci, 2020, 233:103954. |
| [22] | Kang PC, Leng KM, Liu YP, Liu Y, Xu Y, Qin W, Gao JJ, Wang ZD, Tai S, Zhong XY, Cui YF. miR-191 inhibition induces apoptosis through reactivating secreted frizzled- related protein-1 in cholangiocarcinoma. Cell Physiol Biochem, 2018, 49(5):1933-1942. |
| [23] | Sharma S, Nagpal N, Ghosh PC, Kulshreshtha R. P53-miR-191-SOX4 regulatory loop affects apoptosis in breast cancer. RNA, 2017, 23(8):1237-1246. |
| [24] | Tian XY, Xu LM, Wang P. MiR-191 inhibits TNF-α induced apoptosis of ovarian endometriosis and endometrioid carcinoma cells by targeting DAPK1. Int J Clin Exp Pathol, 2015, 8(5):4933-4942. |
| [25] | Varendi K, Kumar A, Härma MA, Andressoo JO. miR-1, miR-10b, miR-155, and miR-191 are novel regulators of BDNF. Cell Mol Life Sci, 2014, 71(22):4443-4456. |
| [26] | Li HX, Du MQ, Xu WM, Wang ZF. MiR-191 downregulation protects against isoflurane-induced neurotoxicity through targeting BDNF. Toxicol Mech Methods, 2021, 31(5):367-373. |
| [27] | Mohammadipoor-Ghasemabad L, Sangtarash MH, Sheibani V, Sasan HA, Esmaeili-Mahani S. Hippocampal microRNA- 191a-5p regulates BDNF expression and shows correlation with cognitive impairment induced by paradoxical sleep deprivation. Neuroscience, 2019, 414:49-59. |
| [28] | Trumpp A, Refaeli Y, Oskarsson T, Gasser S, Murphy M, Martin GR, Bishop JM. c-Myc regulates mammalian body size by controlling cell number but not cell size. Nature, 2001, 414(6865):768-773. |
| [29] | Ramana KV, Tammali R, Srivastava SK. Inhibition of aldose reductase prevents growth factor-induced G1-S phase transition through the AKT/phosphoinositide 3-kinase/ E2F-1 pathway in human colon cancer cells. Mol Cancer Ther, 2010, 9(4):813-824. |
| [30] | Blum Y, Mikelson J, Dobrzynski M, Ryu H, Jacques MA, Jeon NL, Khammash M, Pertz O. Temporal perturbation of ERK dynamics reveals network architecture of FGF2/ MAPK signaling. Mol Syst Biol, 2019, 15(11):e8947. |
| [31] | Strzalka W, Ziemienowicz A. Proliferating cell nuclear antigen (PCNA): a key factor in DNA replication and cell cycle regulation. Ann Bot, 2011, 107(7):1127-1140. |
| [32] | Duval N, Vaslin C, Barata TC, Frarma Y, Contremoulins V, Baudin X, Nedelec S, Ribes VC. BMP4 patterns Smad activity and generates stereotyped cell fate organization in spinal organoids. Development, 2019, 146(14):175430. |
| [33] | Volkmann N, Marassi FM, Newmeyer DD, Hanein D. The rheostat in the membrane: Bcl-2 family proteins and apoptosis. Cell Death Differ, 2014, 21(2):206-215. |
| [34] | Correia C, Lee SH, Meng XW, Vincelette ND, Knorr KLB, Ding HS, Nowakowski GS, Dai HM, Kaufmann SH. Emerging understanding of Bcl-2 biology: implications for neoplastic progression and treatment. Biochim Biophys Acta, 2015, 1853(7):1658-1671. |
| [35] | Savitskaya MA, Onishchenko GE. Mechanisms of apoptosis. Biochemistry (Mosc), 2015, 80(11):1393-1405. |
| [36] | Riera MF, Regueira M, Galardo MN, Pellizzari EH, Meroni SB, Cigorraga SB. Signal transduction pathways in FSH regulation of rat Sertoli cell proliferation. Am J Physiol Endocrinol Metab, 2012, 302(8):E914-E923. |
| [37] | Sun Y, Yang WR, Luo HL, Wang XZ, Chen ZQ, Zhang JJ, Wang Y, Li XM. Thyroid hormone inhibits the proliferation of piglet Sertoli cell via PI3K signaling pathway. Theriogenology, 2015, 83(1):86-94. |
| [38] | Wang C, Zheng P, Adeniran SO, Ma MJ, Huang FS, Adegoke EO, Zhang GX. Thyroid hormone (T3) is involved in inhibiting the proliferation of newborn calf Sertoli cells via the PI3K/Akt signaling pathway in vitro. Theriogenology, 2019, 133:1-9. |
| [39] | Yang WR, Zhu FW, Zhang JJ, Wang Y, Zhang JH, Lu C, Wang XZ. PI3K/Akt activated by GPR30 and Src regulates 17β-estradiol-induced cultured immature boar Sertoli cells proliferation. Reprod Sci, 2017, 24(1):57-66. |
| [40] | Hu PD, Guan KF, Feng Y, Ma CP, Song HB, Li Y, Xia XY, Li JL, Li FG. miR-638 inhibits immature Sertoli cell growth by indirectly inactivating PI3K/AKT pathway via SPAG1 gene. Cell Cycle, 2017, 16(23):2290-2300. |
| [41] | Luo H, Peng FZ, Weng B, Tang XW, Chen Y, Yang AQ, Chen B, Ran ML. miR-222 suppresses immature porcine Sertoli cell growth by targeting the GRB10 gene through inactivating the PI3K/AKT signaling pathway. Front Genet, 2020, 11:581593. |
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