Journal of Peking University(Health Sciences) ›› 2017, Vol. 49 ›› Issue (4): 580-584. doi: 10.3969/j.issn.1671-167X.2017.04.005

• Article • Previous Articles     Next Articles

MicroRNA differential expression profile in tuberous sclerosis complex cell line TSC2-/- MEFs and normal cell line TSC2+/+ MEFs

CAI Yi, GUO Hao, LI Han-zhong, WANG Wen-da, ZHANG Yu-shi△   

  1. (Department of Urology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China)
  • Online:2017-08-18 Published:2017-08-18
  • Contact: ZHANG Yu-shi E-mail:zhangyushi@126.com
  • Supported by:
    Supported by the National Natural Science Foundation of China (81670611) and the Youth Science Foundation of PUMCH (IH1028800)

Abstract: Objective: Tuberous sclerosis complex (TSC) is a multisystem genetic disorder caused by mutations in the TSC1 and TSC2 genes, but the molecular events contributing to TSC are not well understood. However, little is known about the role of microRNAs in TSC. To explore the microRNA differential expression profile between tuberous sclerosis complex cell line TSC2-/- MEFs and normal type cell line TSC2+/+ MEFs, and to provide new clues to study the mechanism of microRNA function in tuberous sclerosis complex. Methods: TSC2-/- MEFs and TSC2+/+ MEFs cell lines were cultured in vitro, each with three samples chosen as the experimental group and the control group respectively. Total RNA was isolated using TRizol and purified with RNeasy mini kit according to manufacturer’s instructions. RNA quality and quantity were measured by using nanodrop spectrophotometer and RNA integrity was determined by gel electrophoresis. Total RNAs were extracted by TRizol, followed by RNA quantification and quality control. MicroRNA profiles were analyzed by microarray and the threshold value used to screen up-regulated more than 2-fold change or down-regulated less than 0.5-fold change compared with controls. Real-time PCR was used to validate the reliability of microarray. Cell counting kit-8 (CCK-8) assay was performed to evaluate the proliferation. Results: Fourteen microRNAs, including miR-18a-5p, miR-376c-3p, miR-136-5p, miR-467c-5p, miR-467b-5p, miR-5104, miR-3098-3p, miR-30a-3p, miR-302b-3p, miR-18a-3p, miR-19b-1-5p, miR-19a-5p, miR-20a-5p, miR-155-5p, were up-regulated, while twenty-six microRNAs, including miR-200b-3p, miR-450a-1-3p, miR-542-5p, miR-199b-5p, miR-10a-5p, miR-466c-5p, miR-450a-5p, miR-450b-5p, miR-542-3p, miR-351-5p, miR-322-3p, miR-199a-3p, miR-335-5p, miR-10b-5p, miR-351-3p, miR-155-3p, miR-497a-5p, miR-503-5p, miR-148a-3p, miR-1843a-5p, miR-199a-5p, miR-490-5p, miR-450a-2-3p, miR-322-5p, miR-214-3p, miR-450b-3p, were downregulated in tuberous sclerosis complex cell line TSC2-/- MEFs compared with normal type cell line TSC2+/+ MEFs (P<0.05). Real-time PCR confirmed the expressions of miR-136-5p, miR-30a-3p, miR-302b-3p, miR-10b-5p, miR-148a-3p, miR-199a-5p consistent with the microarray data (P<0.05). Furthermore, the overexpression of miR-199a-5p significantly inhibited cell proliferation (P<0.05). Conclusion: There are differences in the expression of miRNA between the tube-rous sclerosis complex cell line TSC2-/- MEFs and normal cell line TSC2+/+ MEFs. MiRNA-199a-5p plays an important role in tuberous sclerosis complex, which may be developed as an important molecular target for the treatment of tuberous sclerosis complex.

Key words: Tuberous sclerosis, Cell line, MicroRNAs, Cell proliferation

CLC Number: 

  •  
[1] Yao ZHANG,Jinxin GUO,Shijia ZHAN,Enyu HONG,Hui YANG,Anna JIA,Yan CHANG,Yongli GUO,Xuan ZHANG. Role and mechanism of cysteine and glycine-rich protein 2 in the malignant progression of neuroblastoma [J]. Journal of Peking University (Health Sciences), 2024, 56(3): 495-504.
[2] Wen-gen LI,Xiao-dong GU,Rui-qiang WENG,Su-dong LIU,Chao CHEN. Expression and clinical significance of plasma exosomal miR-34-5p and miR-142-3p in systemic sclerosis [J]. Journal of Peking University (Health Sciences), 2023, 55(6): 1022-1027.
[3] Xiao WANG,Dan HE,Wen-ting LI,SIYITI Adila·,Rui HAN,Ying DONG. Characteristic and clinical significance of microRNA expression between 144 Uygur and Han women with endometrial carcinoma [J]. Journal of Peking University (Health Sciences), 2020, 52(3): 570-577.
[4] Jing XIE,Yu-ming ZHAO,Nan-quan RAO,Xiao-tong WANG,Teng-jiao-zi FANG,Xiao-xia LI,Yue ZHAI,Jing-zhi LI,Li-hong GE,Yuan-yuan WANG. Comparative study of differentiation potential of mesenchymal stem cells derived from orofacial system into vascular endothelial cells [J]. Journal of Peking University(Health Sciences), 2019, 51(5): 900-906.
[5] Jing ZHANG,Su-fang LI,Hong CHEN,Jun-xian SONG. Role of miR-106b-5p in the regulation of gene profiles in endothelial cells [J]. Journal of Peking University(Health Sciences), 2019, 51(2): 221-227.
[6] WANG Zi-cheng, CHENG Li, LV Tong-de, SU Li, LIN Jian, ZHOU Li-qun. Inflammatory priming adipose derived stem cells significantly inhibit the proliferation of peripheral blood mononuclear cells [J]. Journal of Peking University(Health Sciences), 2018, 50(4): 590-594.
[7] TANG Xu, ZHAO Wei-hong, SONG Qin-qin, YIN Hua-qi, DU Yi-qing, SHENG Zheng-zuo, WANG Qiang, ZHANG Xiao-wei, LI Qing, LIU Shi-jun, XU Tao. Influence of SOX10 on the proliferation and invasion of prostate cancer cells [J]. Journal of Peking University(Health Sciences), 2018, 50(4): 602-606.
[8] CHEN Wei, HU Fan-lei, LIU Hong-jiang, XU Li-ling, LI Ying-ni, LI Zhan-guo. Myeloid-derived suppressor cells promoted autologous B cell proliferation in rheumatoid arthritis [J]. Journal of Peking University(Health Sciences), 2017, 49(5): 819-823.
[9] SIMA Zi-han, HONG Ying-ying, LI Tie-jun△. Effects of PTCH1 mutations on the epithelial proliferation derived from keratocystic odontogenic tumour [J]. Journal of Peking University(Health Sciences), 2017, 49(3): 522-526.
[10] GAO Xiang, CHEN Xiang-mei, ZHANG Ting, ZHANG Jing, CHEN Mo, GUO Zheng--yang, SHI Yan-yan, LU Feng-min, DING Shi-gang. Relationship between macrophage capping protein and gastric cancer cell’s proliferation and migration ability [J]. Journal of Peking University(Health Sciences), 2017, 49(3): 489-494.
[11] YANG Di, XU Jun-hui, DENG Fu-rong△, GUO Xin-biao . Effects of silver nanoparticle on hemichannel activation and anti-proliferation in HaCaT cells [J]. Journal of Peking University(Health Sciences), 2017, 49(3): 371-375.
[12] SUI Hua-xin, LV Pei-jun, WANG Yu-guang, WANG Yong, SUN Yu-chun. Effect of lowlevel laser irradiation on proliferation and osteogenic differentiation of human adipose-derived stromal cells [J]. Journal of Peking University(Health Sciences), 2017, 49(2): 337-343.
[13] LI Jing-wen, YIN Xiao-hui, LUAN Qing-xian. Comparative study of proliferative and periodontal differentiation propensity of induced pluripotent stem cells at different passages [J]. Journal of Peking University(Health Sciences), 2017, 49(1): 16-024.
[14] LING Long, ZHAO Yu-ming, GE Li-hong. Impact of different degree pulpitis on cell proliferation and osteoblastic differentiation of dental pulp stem cell in Beagle immature premolars [J]. Journal of Peking University(Health Sciences), 2016, 48(5): 878-883.
[15] HU Jia,ZOU Xiao-ying,ZHUANG Heng,GAO Xue-jun. Effect of root canal sealers on biocompatibility of human periodontal ligament cells [J]. Journal of Peking University(Health Sciences), 2016, 48(5): 871-877.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!