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患者临床未受累皮肤的皮肤改变

Dermal Alterations in Clinically Unaffected Skin of Patients.

作者信息

Boraldi Federica, Lofaro Francesco Demetrio, Losi Lorena, Quaglino Daniela

机构信息

Department of Life Sciences, University of Modena and Reggio Emilia, Via Campi, 287, 41125 Modena, Italy.

出版信息

J Clin Med. 2021 Feb 1;10(3):500. doi: 10.3390/jcm10030500.

Abstract

BACKGROUND

Pseudoxanthoma elasticum (PXE), due to rare sequence variants in the gene, is characterized by calcification of elastic fibers in several tissues/organs; however, the pathomechanisms have not been completely clarified. Although it is a systemic disorder on a genetic basis, it is not known why not all elastic fibers are calcified in the same patient and even in the same tissue. At present, data on soft connective tissue mineralization derive from studies performed on vascular tissues and/or on clinically affected skin, but there is no information on patients' clinically unaffected skin.

METHODS

Skin biopsies from clinically unaffected and affected areas of the same PXE patient (n = 6) and from healthy subjects were investigated by electron microscopy. Immunohistochemistry was performed to evaluate p-SMAD 1/5/8 and p-SMAD 2/3 expression and localization.

RESULTS

In clinically unaffected skin, fragmented elastic fibers were prevalent, whereas calcified fibers were only rarely observed at the ultrastructural level. p-SMAD1/5/8 and p-SMAD2/3 were activated in both affected and unaffected skin.

CONCLUSION

These findings further support the concept that fragmentation/degradation is necessary but not sufficient to cause calcification of elastic fibers and that additional local factors (e.g., matrix composition, mechanical forces and mesenchymal cells) contribute to create the pro-osteogenic environment.

摘要

背景

弹性假黄瘤(PXE)由于该基因中罕见的序列变异,其特征是多个组织/器官中的弹性纤维钙化;然而,发病机制尚未完全阐明。尽管它是一种基于遗传的全身性疾病,但尚不清楚为什么在同一患者甚至同一组织中并非所有弹性纤维都会钙化。目前,关于软结缔组织矿化的数据来自对血管组织和/或临床受累皮肤的研究,但尚无关于患者临床未受累皮肤的信息。

方法

对同一PXE患者(n = 6)临床未受累和受累区域的皮肤活检组织以及健康受试者的皮肤活检组织进行电子显微镜检查。进行免疫组织化学以评估p-SMAD 1/5/8和p-SMAD 2/3的表达和定位。

结果

在临床未受累皮肤中,破碎的弹性纤维很普遍,而在超微结构水平仅很少观察到钙化纤维。p-SMAD1/5/8和p-SMAD2/3在受累和未受累皮肤中均被激活。

结论

这些发现进一步支持了这样的概念,即断裂/降解是导致弹性纤维钙化的必要但不充分条件,并且其他局部因素(例如基质组成、机械力和间充质细胞)有助于形成促骨生成环境。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32c1/7867076/b7479170080d/jcm-10-00500-g001.jpg

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