瘢痕疙瘩瘙痒相关分子的微阵列研究

M. Asai, Y. Koike, Y. Kuwatsuka, K. Kashiyama, Katsumi Tanaka, A. Utani, H. Murota
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引用次数: 0

摘要

瘢痕疙瘩常伴有瘙痒。由于抓挠等创伤刺激会促进瘢痕疙瘩扩大,缓解瘙痒是瘢痕疙瘩治疗的一个重要方面。为了研究瘢痕疙瘩瘙痒的机制,我们对瘢痕疙瘩和非瘢痕疙瘩皮肤进行了基于微阵列的比较。测定了瘙痒相关配体和受体的相对表达水平,然后构建了一个专注于5-羟色胺能信号传导的热图,最后进行了通路分析。结果显示瘢痕疙瘩病变中各种转录物的相对上调,包括编码组胺受体(H1R)、5-羟色胺受体(5-HT-2A)和内皮素受体(ET-a)的转录物。5-羟色胺能信号传导可能与瘢痕疙瘩瘙痒有关。
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Microarray-based exploration of molecules associated with keloid pruritus
Keloids are frequently accompanied with pruritus. Because traumatic stimuli such as scratching promotes keloid enlargement, alleviating pruritus is an important aspect of keloid management. To investigate the mechanism of keloid pruritus, we conducted a microarray-based comparison of keloid and nonkeloid skin. Relative expression levels of pruritus-associated ligands and receptors were determined, followed by construction of a heat map focused on serotonergic signaling, and finally pathway analysis. Results demonstrate relative up-regulation of various transcripts within keloid lesions, including those encoding a histamine receptor (H1R), a serotonin receptor (5-HT-2A), and an endothelin receptor (ET-A). Serotonergic signaling may be involved in keloid pruritus.
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