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Th1/Th2 细胞趋化因子表达在肥厚性瘢痕中的作用。

The role of Th1/Th2 cell chemokine expression in hypertrophic scar.

机构信息

Department of Burs and Plastic Surgery, The Forth Medical Center of PLA General Hospital, Beijing, China.

Department of Plastic and Reconstructive Surgery, The Formerly Forth Military Medical Hospital, Xi'an, China.

出版信息

Int Wound J. 2020 Feb;17(1):197-205. doi: 10.1111/iwj.13257. Epub 2019 Nov 5.

Abstract

The aim of this study was to study the role of Th1/Th2 cell-associated chemokines in the formation of hypertrophic scars in rabbit ears. Twenty-six New Zealand white rabbits were used to establish the hypertrophic scar model of rabbit ear and the normal scar model of rabbit's back. Two rabbits were sacrificed on days 0 and 21, 28, 35, 42, 49, 56, and 63 after operation. The specimens were stained with haematoxylin-eosin (HE). Scar elevation index (SEI) was used to detect the expression of 10 chemokines related to Th1/Th2 cells in both scar formation expressions. Real-time polymerase chain reaction (PCR) results showed that two chemokines (CXCL10, CXCL12) were highly expressed during the formation of normal scar, and there was almost no expression during the formation of hypertrophic scar (*P < 0.05). The chemokines (CCL2, CCL3, CCL4, CCL5, CCL7, CCL13, CX3CL1) were almost non-expressed in the formation of normal scars but were expressed for a long time in the formation of hypertrophic scars. The four chemokines, CCL2, CCL4, CCL5, and CX3CL1, maintained a long-term high expression level during the formation of hypertrophic scars (P < 0.01). There were also three chemokines (CCL14, CCL19, CCL21) that were almost undetectable in normal scarring, but there was transiently low-level expression (P < 0.05) only during the peak proliferative phase in proliferative scarring. Th1/Th2 cell-associated chemokines are different in the type, quantity and expression, and maintenance time of rabbit ear hypertrophic scars.

摘要

本研究旨在探讨 Th1/Th2 细胞相关趋化因子在兔耳增生性瘢痕形成中的作用。采用 26 只新西兰白兔建立兔耳增生性瘢痕模型和兔背部正常瘢痕模型,术后 0、21、28、35、42、49、56、63 天分别处死 2 只兔,采用苏木精-伊红(HE)染色。瘢痕隆起指数(SEI)检测 10 种与 Th1/Th2 细胞相关的趋化因子在两种瘢痕形成中的表达。实时聚合酶链反应(PCR)结果显示,两种趋化因子(CXCL10、CXCL12)在正常瘢痕形成过程中高表达,而在增生性瘢痕形成过程中几乎无表达(*P < 0.05)。趋化因子(CCL2、CCL3、CCL4、CCL5、CCL7、CCL13、CX3CL1)在正常瘢痕形成过程中几乎不表达,但在增生性瘢痕形成过程中表达时间较长。四种趋化因子 CCL2、CCL4、CCL5 和 CX3CL1 在增生性瘢痕形成过程中维持长期高水平表达(P < 0.01)。还有三种趋化因子(CCL14、CCL19、CCL21)在正常瘢痕形成中几乎检测不到,但在增生性瘢痕的增殖高峰期有短暂的低水平表达(P < 0.05)。兔耳增生性瘢痕中 Th1/Th2 细胞相关趋化因子的类型、数量、表达和维持时间不同。

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