JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES) ›› 2015, Vol. 53 ›› Issue (3): 50-55.doi: 10.6040/j.issn.1671-7554.0.2014.690

Previous Articles     Next Articles

Proliferative effect of TGF-β1 phage model peptide on fibroblasts

LIU Zhenzhong1, JIANG Duyin1, WANG Wei1, ZONG Xianlei2, ZHANG Jixun1, LIU Lei1   

  1. 1. Department of Plastic Surgery, the Second Hospital of Shandong University, Jinan 250033, Shandong, China;
    2. Sixteenth Department of Plastic Surgery Hospital, Chinese Academy of Medical Sciences, Beijing 100144, China
  • Received:2014-10-13 Revised:2015-01-14 Online:2015-03-10 Published:2015-03-10

Abstract: Objective To isolate transforming growth factor-beta1 (TGF-β1) phage model peptides from phage display 12-mer peptide library, and to evaluate their proliferative effect on normal skin fibroblasts. Methods Phage 12-mer display peptide library was screened with monoclonal anti-human TGF-β1 to get specific phage model peptides. The model with sequence most similar to TGF-β1 was chosen and 4 groups were enrolled:negative control group, MP13 control group, TGF-β1 control group, and phage model peptide group. MTT assay was used for the quantitative determination of cellular proliferation. Immunofluorescence assay was employed to show the affinity of the model peptide on skin fibroblasts. Quantitative Real-time PCR analysis was carried out to detect the expressions of I collagen (COL1), III collagen (COL3) and connective tissue growth factor (CTGF). Results A total of 10 phage model peptides were obtained. The first one with sequence most similar to TGF-β1 was chosen. The MTT results showed that the phage model peptide could promote fibroblast proliferation (P<0.05). Immunofluorescence assay revealed that the model peptide on phages rather than phages could bind to the fibroblasts (P<0.05). The Real-time PCR analysis suggested that the relative expressions of COL1 and COL3 significantly increased in the model group than in the negative control group and M13 group (P<0.05). The expression of CTGF mRNA increased dramatically after treatment withphage model peptide, and reached the peak at 2 d (P<0.05). Conclusion The phage model peptide isolated from phage 12-mer display peptide library can promote the proliferation of normal skin fibroblasts by regulating the expression of CTGF.

Key words: Peptide library, Phage display, Transforming growth factor-beta1, Fibroblasts, Proliferation

CLC Number: 

  • R622
[1] Kolluri R. Management of venous ulcers[J]. Tech Vasc Interv Radiol, 2014, 17(2):132-138.
[2] Richmond NA, Maderal AD, Vivas AC. Evidence-based management of common chronic lower extremity ulcers[J]. Dermatol Ther, 2013, 26(3):187-196.
[3] Game FL, Hinchliffe RJ, Apelqvist J, et al. A systematic review of interventions to enhance the healing of chronic ulcers of the foot in diabetes[J]. Diabetes Metab Res Rev, 2012, 28(suppl 1):119-141.
[4] Barrientos S, Brem H, Stojadinovic O, et al. Clinical application of growth factors and cytokines in wound healing[J]. Wound Repair Regen, 2014, 22(5):569-578.
[5] Efron PA, Moldawer LL. Cytokines and wound healing:the role of cytokine and anticytokine therapy in the repair response[J]. J Burn Care Rehabi, 2004, 25(2):149-160.
[6] Raffetto JD. Which dressings reduce inflammation and improve venous leg ulcer healing. Phlebology[J]. 2014, 29(1suppl):157-164.
[7] 刘振中, 姜笃银, 蔡景龙, 等. 转化生长因子-β1噬菌体模拟肽抑制瘢痕疙瘩成纤维细胞增殖的实验研究[J]. 中华医学杂志, 2011, 91(38):2714-2718. LIU Zhenzhong, JIANG Duyin, CAI Jinglong, et al. Study of TGF-β1 phage model peptides on inhibiting keloid fibroblasts proliferation[J]. National Medical Journal of China, 2011, 91(38):2714-2718.
[8] 刘振中, 姜笃银, 蔡景龙, 等. 应用噬菌体随机十二肽库筛选TGF-β1相关模拟肽的实验研究[J]. 山东大学学报:医学版, 2011, 49(8):70-73. LIU Zhenzhong, JIANG Duyin, CAI Jinglong, et al. TGF-β1-related model peptides isolated form a phage display 12-mer peptide library[J]. Journal of Shandong University:Health Sciences, 2011, 49(8):70-73.
[9] Maroni D, Davis JS. Transforming growth factor beta 1 stimulates profibrotic activities of luteal fibroblasts in cows[J]. Biol Reprod, 2012, 87(5):127.
[10] Jiang L, Dai Y, Cui F, et al. Expression of cytokines, growth factors and apoptosis-related signal molecules in chronic pressure ulcer wounds healing[J]. Spinal Cord, 2014, 52(2):145-151.
[11] Ebrahimizadeh W, Rajabibazl M. Bacteriophage vehicles for phage display:biology, mechanism and application[J]. Curr Microbiol, 2014, 69(2):109-120.
[12] El Gazaerly H, Elbardisey DM, Eltokhy HM, et al. Effect of transforming growth factor beta 1 on wound healing in induced diabetic rats[J]. Int J Health Sci (Qassim), 2013, 7(2):160-172.
[13] Pakyari M, Farrokhi A, Maharlooei MK, et al. Critical role of transforming growth factor beta in different phases of wound healing[J]. Adv Wound Care (New Rochelle), 2013, 2(5):215-224.
[14] 王文婷, 单菲, 王晓川, 等. TGF-β1对糖尿病大鼠深II度烫伤创面愈合的影响[J]. 山东大学学报:医学版, 2011, 49(7):19-23. WANG Wenting, SHAN Fei, WANG Xiaochuan, et al. Effects of TGF-β1 on wound healing in diabetic rats with second-degree scald[J]. Journal of Shandong University:Health Sciences, 2011, 49(7):19-23.
[15] Finnson KW, McLean S, Di Guglielmo GM, et al. Dynamics of transforming growth factor beta signaling in wound healing and scarring[J]. Adv Wound Care (New Rochelle), 2013, 2(5):195-214.
[16] Weiss A, Attisano L. The TGFbeta superfamily signaling pathway[J]. Wiley Interdiscip Rev Dev Biol, 2013, 2(1):47-63.
[17] Barrientos S, Stojadinovic O, Golinko MS, et al. Growth factors and cytokines in wound healing[J]. Wound Repair Regen, 2008, 16(5):585-601.
[1] WANG Xiao-Lei, ZHANG Hai-Thao, ZHANG Hui, GUO Cheng-Hao. Protective effects of shuxuening injecta on vascular  endothelial  cell injury in vitro due to iodine excesses [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2209, 47(6): 38-.
[2] SUN Yifeng, GAO Yu, LIANG Yongyuan, GAO Yang. Expression of CPLX2 and its in vitro effects on the proliferation migration and invasion of hepatocellular carcinoma cells [J]. Journal of Shandong University (Health Sciences), 2020, 1(9): 34-39.
[3] ZHANG Baowen, LEI Xiangli, LI Jinna, LUO Xiangjun, ZOU Rong. miR-21-5p targeted TIMP3 to inhibit proliferation and extracellular matrix accumulation of mesangial cells in Type II diabetic nephropathy mice [J]. Journal of Shandong University (Health Sciences), 2020, 1(7): 7-14.
[4] MA Qingyuan, PU Peidong, HAN Fei, WANG Chao, ZHU Zhoujun, WANG Weishan, SHI Chenhui. Effect of miR-27b-3p regulating SMAD1 on osteosarcoma cell proliferation, migration and invasion [J]. Journal of Shandong University (Health Sciences), 2020, 1(7): 32-37.
[5] LI Ning, LI Juan, XIE Yan, LI Peilong, WANG Yunshan, DU Lutao, WANG Chuanxin. Expression of LncRNA AL109955.1 in 80 cases of colorectal cancer and its effect on cell proliferation, migration and invasion [J]. Journal of Shandong University (Health Sciences), 2020, 1(7): 38-46.
[6] WANG Kaimin, TAN Juanjuan, YAN Zhiqiang, LI Zhiqiang. Effects of Sirtuin on hypoxia-induced proliferation of human umbilical cord-derived mesenchymal stem cells [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2017, 55(7): 23-30.
[7] SHI Peikun, ZENG Beini, WU Weifang, HU Xiaoyan, MA Tianjia, ZHOU Yabin. Expression and role of Keap1 in renal cell carcinoma [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2017, 55(3): 94-99.
[8] SUN Zeyu, CHEN Ying, LIN Jiaxiang, LIU Juan, ZHAO Weiming. Influence of inositol polyphosphate-4-phosphatase type II on the proliferation and apoptosis of cervical cancer cells [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2017, 55(11): 1-6.
[9] WANG Tiantian, CHEN Jie. Expression and clinical significance of EFEMP2 in endometrial cancer tissues and cell [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2017, 55(10): 52-58.
[10] ZHAO Lu, JIAO Jun, ZHANG Teng, JIAO Xinlin, CUI Baoxia. Expression of LXRα in ovarian carcinoma and effects of T0901317 on SKOV3 cell line [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2017, 55(1): 49-53.
[11] TIAN Siqi, LIU Riqiang, YANG Ning, WEI Wei, YANG Huawei. Effect of expression of ribosomal protein S6 Kinase 4 variants on the proliferation of breast cancer cell MDA-MB-231 [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2016, 54(9): 32-36.
[12] LU Zhenzhen, YAN Lei, ZHANG Hui, ZHANG Xiaohui, ZHAO Xingbo. Effects of TGF β-1 on the activation of endometrial stromal cells in tumor microenvironment [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2016, 54(9): 37-40.
[13] WEI Xiujuan, WU Xiuyin, TONG Dongdong, LI Jing, YANG Xiaolu, ZHANG Fenghe. Expression of BDNF/TrkB and effect of BDNF on the proliferation ability of tongue squamous cell carcinoma [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2016, 54(6): 50-54.
[14] ZHAO Yunxia, SONG Jing, ZHANG Cancan, LIN Xueyan, WEI Wei, TIAN Yongjie. CXXC4 promotes sensitivity to chemotherapy drugs in epithelial ovarian cancer cells [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2016, 54(3): 24-29.
[15] CHEN Yan, LIU Juan, CHEN Hanxiang, ZHANG Weifang, ZHAO Weiming. Effects of miR-17 on the senescence of human foreskin fibroblasts [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2015, 53(5): 55-59.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!