[PDGF-C对人真皮乳头细胞生物学特性的影响]。

中华整形外科杂志 Pub Date : 2016-05-01
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引用次数: 0

摘要

目的:探讨血小板源性生长因子- c (PDGF-C)对体外培养的人毛乳头细胞生物学特性的影响。方法:从除皱术获得的人发皮中分离人真皮乳头细胞,并进行体外培养。采用细胞计数和CCK-8法检测PDGF-C(0、10、20、30和40ng/ml)在0、1 d、2d、3d、4d、5d、6d对HDPCs增殖的影响。在最佳浓度下,流式细胞术检测细胞相。Transwell法和细胞划痕法检测细胞迁移。采用碱性磷酸酶活性测定试剂盒检测HDPCs的诱导活性。结果:PDGF-C显著诱导HDPCs增殖。30ng/mL的PDGF-C对HDPCs增殖有峰值促进作用,使阻滞在S期的细胞比例增加(P < 0.05)。PDGF-C也增加了培养HDPCs的迁移种群。30ng/ml PDGF-C处理组跨井插入膜下侧细胞数为(361.3±24.95)个,对照组为(246.8±7.525)个,差异有统计学意义(P < 0.05)。与对照组相比,培养HDPCs的碱性磷酸盐活性升高,差异显著(P < 0.05)。结论:PDGF-C能促进体外培养的人真皮乳头细胞的增殖、迁移和诱导活性,可能有利于促进人真皮乳头细胞的体外培养。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Effect of PDGF-C on biological characters of human dermal papilla cells in vitro].

Objective: To determine the effect of platelet-derived growth factor-C (PDGF-C) on biological characters of human hair dermal papilla cells cultured in vitro.

Methods: The human dermal papilla cells(HDPCs) were isolated from human hair skin obtained from rhytidectomy procedure and then cultured in vitro. Cell counting and CCK-8 assay were used to detect the effects of PDGF-C (0,10,20,30 and 40ng/ml) on the proliferation of HDPCs at 0,1 d,2d,3d,4d,5d,6d.Under the optimal concentration, flow cytometry was used to detect cell phases. Transwell assay and cell scratch test were performed to detect cell migration. Alkaline Phosphatase Activity Assay kit was used to detect the inductive activity of HDPCs.

Results: PDGF-C significantly induced the proliferation of HDPCs. PDGF-C of 30ng/mL promoted the HDPCs proliferation at a summit and increased the percentage of the cells arrested at S phase (P < 0.05).PDGF-C also increased the migration populations of cultured HDPCs. The cell number in lower side of the transwell insert membrane of 30ng/ml PDGF-C treated group was (361.3 ± 24.95)while the control was (246.8 ± 7.525),showing significant difference (P < 0.05).The alkaline phosphate activity of cultured HDPCs was increased comparing to the control group, the difference was significant (P < 0.05).

Conclusions: PDGF-C can promote the proliferation, migration and inductive activity of cultured human dermal papilla cells, which might be beneficial to promote the cultivation of human dermal papilla cells in vitro.

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