Gillies McIndoe Research Institute, Wellington, New Zealand.
J Clin Pathol. 2013 Jul;66(7):597-600. doi: 10.1136/jclinpath-2012-201096. Epub 2013 Apr 4.
Recent reports on infantile haemangioma (IH) have demonstrated a primitive population of interstitial cells expressing the embryonic transcription factor, Nanog, with decreasing abundance during involution. In this report we investigated the expression of Nanog on mast cells in all three phases of IH progression.
Paraffin-embedded sections of six proliferating, six involuting and six involuted IH lesions were used to investigate the expression of tryptase, Nanog, CD45, CD34 and GLUT-1 by immunostaining.
Mast cells, identified by their expression of tryptase, were located in the interstitium of IH lesions. 93%, 42% and 0% of these tryptase(+) cells also expressed Nanog, in proliferating, involuting and involuted IH, respectively.
The identification of an abundant population of tryptase(+)/Nanog(+) cells in IH is novel. The relative loss of Nanog expression as IH involutes may be a result of maturation and/or proliferation of these cells. This report supports the primitive nature of IH.
最近关于婴儿血管瘤(IH)的报告表明,间充质细胞中存在表达胚胎转录因子 Nanog 的原始细胞群,在退化过程中其丰度逐渐降低。在本报告中,我们研究了 Nanog 在 IH 进展的所有三个阶段中对肥大细胞的表达。
使用 6 例增殖期、6 例退化期和 6 例退化期 IH 病变的石蜡包埋切片,通过免疫染色检测嗜碱性粒细胞的 tryptase、Nanog、CD45、CD34 和 GLUT-1 的表达。
通过 tryptase 的表达鉴定出的肥大细胞位于 IH 病变的间质中。在增殖期、退化期和退化期 IH 中,分别有 93%、42%和 0%的这些 tryptase(+)细胞也表达 Nanog。
在 IH 中鉴定出大量的 tryptase(+)/Nanog(+)细胞是新颖的。随着 IH 的退化,Nanog 表达的相对丧失可能是这些细胞成熟和/或增殖的结果。本报告支持 IH 的原始性质。