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转化生长因子-β1和血小板衍生生长因子对牙周膜细胞和牙龈成纤维细胞增殖的差异作用。

Differential effect of TGF-beta 1 and PDGF on proliferation of periodontal ligament cells and gingival fibroblasts.

作者信息

Dennison D K, Vallone D R, Pinero G J, Rittman B, Caffesse R G

机构信息

Division of Periodontics, University of Texas Houston-Health Science Center, USA.

出版信息

J Periodontol. 1994 Jul;65(7):641-8. doi: 10.1902/jop.1994.65.7.641.

Abstract

Regeneration of periodontal tissues requires orchestration of several cell types. Two cell types, gingival fibroblastic cells (gingival fibroblasts) and cells from the periodontal ligament (PDL cells), were studied to compare the effects of supplemental addition of TGF-beta 1 and PDGF on proliferation. Cells obtained from healthy donors were cultured in 10% FBS supplemented with either 10 ng/ml TGF-beta 1, 20 ng/ml PDGF, or both. Thymidine incorporation was measured after 24, 48, or 72 hours. Data from PDL (analyzed by ANOVA) showed the following relations: at 24 hours TGF beta 1/PDGF = PDGF > TGF-beta 1 = control; at 48 hours TGF beta 1/PDGF > TGF-beta 1 > PDGF > control; at 72 hours TGF beta 1/PDGF > TGF-beta 1 > PDGF = control. Gingival fibroblast cultures showed the following relations: at 24 and 48 hours TGF beta 1/PDGF = PDGF > TGF-beta 1 = control; at 72 hours, TGF beta 1/PDGF = PDGF > control with TGF beta 1 not different from control or factor combinations. Both TGF-beta 1 and TGF-beta 1/PDGF showed a significantly greater increase in proliferation of PDL cells than in gingival fibroblasts at 48 and 72 hours (Student t test P < 0.05). In contrast, PDGF stimulated proliferation of gingival fibroblasts was significantly greater than PDL cells at 72 hours (P < 0.05). Thus, supplementation of complete cultures (containing 10% FBS) with TGF-beta 1 alone or combined with PDGF stimulates proliferation of PDL cells to a significantly greater extent than proliferation of gingival fibroblasts.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

牙周组织的再生需要多种细胞类型协同作用。研究了两种细胞类型,即牙龈成纤维细胞(牙龈成纤维细胞)和牙周膜细胞(PDL细胞),以比较补充转化生长因子β1(TGF-β1)和血小板衍生生长因子(PDGF)对细胞增殖的影响。从健康供体获取的细胞在补充有10 ng/ml TGF-β1、20 ng/ml PDGF或两者的10%胎牛血清(FBS)中培养。在24、48或72小时后测量胸腺嘧啶核苷掺入量。PDL细胞的数据(通过方差分析)显示出以下关系:在24小时时,TGF-β1/PDGF = PDGF > TGF-β1 = 对照;在48小时时,TGF-β1/PDGF > TGF-β1 > PDGF > 对照;在72小时时,TGF-β1/PDGF > TGF-β1 > PDGF = 对照。牙龈成纤维细胞培养显示出以下关系:在24和48小时时,TGF-β1/PDGF = PDGF > TGF-β1 = 对照;在72小时时,TGF-β1/PDGF = PDGF > 对照,TGF-β1与对照或因子组合无差异。在48和72小时时,TGF-β1和TGF-β1/PDGF均显示PDL细胞增殖的增加显著大于牙龈成纤维细胞(学生t检验,P < 0.05)。相反,在72小时时,PDGF刺激的牙龈成纤维细胞增殖显著大于PDL细胞(P < 0.05)。因此,在完全培养基(含10% FBS)中单独补充TGF-β1或与PDGF联合补充,对PDL细胞增殖的刺激程度显著大于对牙龈成纤维细胞增殖的刺激程度。(摘要截短于250字)

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