The Antimicrobial Peptide Nal-P-113 Exerts a Reparative Effect by Promoting Cell Proliferation, Migration, and Cell Cycle Progression.

Objective. The primary purpose of this study was to evaluate the reparative efficacy of a novel antimicrobial peptide, Nal-P-113, in shortening the healing time of oral mucosal ulcers by promoting cell proliferation and migration and accelerating the cell cycle. Methods. Cell counting kit-8 (CCK-8)...

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Publicado en:BioMed Research International Vol. 2018; pp. 1 - 11
Autores principales: Liu, Nana, Guan, Shuo, Wang, Hongyan, Li, Chen, Cheng, Jyawei, Yu, Huiyuan, Lin, Li, Pan, Yaping
Formato: pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell 9/12/2018
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 9/12/2018
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1155/2018/7349351
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        atl: The Antimicrobial Peptide Nal-P-113 Exerts a Reparative Effect by Promoting Cell Proliferation, Migration, and Cell Cycle Progression.
      aug:
        au:
          Liu, Nana
          Guan, Shuo
          Wang, Hongyan
          Li, Chen
          Cheng, Jyawei
          Yu, Huiyuan
          Lin, Li
          Pan, Yaping
        affil: Department of Periodontics, School of Stomatology, China Medical University, Shenyang 110002, China
      sug:
        subj:
          Antimicrobial Peptides
          Antiinfective Agents
          Cell Proliferation
          Cell Cycle Physiology
          Cell Migration Assays
          Human
          Oral Health
          Stomatitis, Aphthous Therapy
          Wound Healing
          Polymerase Chain Reaction
          Acetic Acid
          Epidermal Growth Factors
          Transforming Growth Factor beta
          Fibroblasts
      ab: Objective. The primary purpose of this study was to evaluate the reparative efficacy of a novel antimicrobial peptide, Nal-P-113, in shortening the healing time of oral mucosal ulcers by promoting cell proliferation and migration and accelerating the cell cycle. Methods. Cell counting kit-8 (CCK-8) and wound-healing assays were used to evaluate the proliferation and migration of human immortalized oral epithelial cells (HIOECs). The cell cycle distribution of HIOECs was analyzed by flow cytometry. Additionally, the RNA levels of EGF, FGF-2, and TGF-β1 of HIOECs were assessed by real-time PCR. Rats were divided into three groups randomly: (a) blank control group; (b) 20 μg/mL Nal-P-113; and (c) 10 ng/mL rhEGF. An oral mucosal ulcer was induced in every rat by the application of 30% acetic acid. An immunohistochemical assay was used to assess the expression of EGF, FGF-2, and TGF-β1 in the rat oral mucosa. Results. In the CCK-8 assay, the optical density values in the Nal-P-113 and rhEGF groups were found to be significantly higher than that in the blank control group. In addition, the scratch areas in the Nal-P-113 and rhEGF groups were found to be significantly smaller (P<0.05). Cell cycle analysis showed that Nal-P-113 accelerated the entry of HIOECs into the S phase and expedited their cell cycles. The RT-PCR results suggested that Nal-P-113 upregulated the RNA levels of EGF and FGF-2 but downregulated that of TGF-β1 at 24 h and 48 h. Lastly, the immunohistochemical assay verified that Nal-P-113 changed the expression of the above cytokines in rat mucosal ulcers. Conclusion. Nal-P-113 promoted the repair of oral mucosal ulcers by increasing the EGF and FGF-2 expression and decreasing that of TGF-β1 in HIOECs, accelerating their proliferation and cell cycle progression. The application of Nal-P-113 might serve as an effective therapeutic approach for recurrent aphthous stomatitis.
      pubtype: Academic Journal
      doctype:
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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