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牙本质涎磷蛋白结构域介导人牙周膜干细胞的增殖和分化。

Domain of dentine sialoprotein mediates proliferation and differentiation of human periodontal ligament stem cells.

机构信息

Department of Developmental Dentistry, Dental School, The University of Texas Health Science Center at San Antonio, San Antonio, Texas, United States of America ; Department of Orthodontics, YüzüncüYıl University, Faculty of Dentistry, Kampus-Van, Turkey.

State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST) and Key Laboratory for Oral Biomedicine of Ministry of Education, School and Hospital of Stomatology, Wuhan University, Wuhan, China.

出版信息

PLoS One. 2013 Dec 3;8(12):e81655. doi: 10.1371/journal.pone.0081655. eCollection 2013.

Abstract

Classic embryological studies have documented the inductive role of root dentin on adjacent periodontal ligament differentiation.  The biochemical composition of root dentin includes collagens and cleavage products of dentin sialophosphoprotein (DSPP), such as dentin sialoprotein (DSP).  The high abundance of DSP in root dentin prompted us to ask the question whether DSP or peptides derived thereof would serve as potent biological matrix components to induce periodontal progenitors to further differentiate into periodontal ligament cells. Here, we test the hypothesis that domain of DSP influences cell fate. In situ hybridization and immunohistochemical analyses showed that the COOH-terminal DSP domain is expressed in mouse periodontium at various stages of root development. The recombinant COOH-terminal DSP fragment (rC-DSP) enhanced attachment and migration of human periodontal ligament stem cells (PDLSC), human primary PDL cells without cell toxicity. rC-DSP induced PDLSC cell proliferation as well as differentiation and mineralization of PDLSC and PDL cells by formation of mineralized tissue and ALPase activity. Effect of rC-DSP on cell proliferation and differentiation was to promote gene expression of tooth/bone-relate markers, transcription factors and growth factors. The results for the first time showed that rC-DSP may be one of the components of cell niche for stimulating stem/progenitor cell proliferation and differentiation and a natural scaffold for periodontal regeneration application.

摘要

经典的胚胎学研究已经证明了根牙本质在相邻牙周韧带分化中的诱导作用。根牙本质的生化组成包括胶原蛋白和牙本质涎磷蛋白 (DSPP) 的裂解产物,如牙本质涎蛋白 (DSP)。根牙本质中 DSP 的高丰度促使我们提出这样一个问题,即 DSP 或其衍生肽是否可以作为有效的生物基质成分,诱导牙周祖细胞进一步分化为牙周韧带细胞。在这里,我们检验了 DSP 结构域影响细胞命运的假设。原位杂交和免疫组织化学分析表明,COOH 端的 DSP 结构域在小鼠牙周组织的根发育的各个阶段都有表达。重组的 COOH 端 DSP 片段 (rC-DSP) 增强了人牙周韧带干细胞 (PDLSC) 的黏附和迁移,而对人原代牙周韧带细胞没有细胞毒性。rC-DSP 通过形成矿化组织和碱性磷酸酶 (ALPase) 活性,诱导 PDLSC 细胞增殖以及 PDLSC 和 PDL 细胞的分化和矿化。rC-DSP 对细胞增殖和分化的影响是促进与牙齿/骨骼相关的标记物、转录因子和生长因子的基因表达。这些结果首次表明,rC-DSP 可能是刺激干细胞/祖细胞增殖和分化的细胞生态位的组成部分之一,也是牙周再生应用的天然支架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0923/3882282/746efe513760/pone.0081655.g001.jpg

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