کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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3214565 | 1203304 | 2006 | 9 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Vascular anomalies in lipoid proteinosis (hyalinosis cutis et mucosae): Basement membrane components and ultrastructure Vascular anomalies in lipoid proteinosis (hyalinosis cutis et mucosae): Basement membrane components and ultrastructure](/preview/png/3214565.png)
SummaryBackgroundIn lipoid proteinosis (LP) vascular anomalies represent severe functional defects caused by excessive deposition of basement membrane (BM)-like matrix, particularly around small subepithelial blood vessels.ObjectiveCorrelation of microvascular anomalies in morphology and ultrastructure with extracellular matrix composition and cell interactions for elucidating vascular involvement in LP-pathophysiology.MethodsBiopsies from non-related LP-patients were analyzed by indirect immunofluorescence (IIF), electron microscopy (EM), and immune-EM (ImEM).ResultsIn LP-skin and mucosa the thickened vessel walls stained strongly for the BM-components type IV collagen, laminin, perlecan, and nidogen (IIF). Integrin α6β4 was regularly collocated with endothelial surface markers such as PECAM (CD31). Ultrastructure (EM) revealed highly ordered matrix deposits around microvessels, with frequently collapsed lumina, functionally compensated by increased vascular density (histology, IIF). Pericytes were trapped between these concentric BM-layers at varying distances towards the periphery (EM), contrasting their regularly close endothelial apposition. Periodic type IV collagen patterns (ImEM) corroborated the multiple BM-leaflet structure and the lack of a common ‘fused’ endothelial–pericyte BM, seen normally. Presumptive secretory vesicles, abundant in both cell types, implied an equal contribution to BM-synthesis, but also indicated partial loss of endothelial polarity.ConclusionsIn LP thickened vessel walls, composed of multiple BM, profoundly alter microvascular properties, also by interference with endothelial–pericyte interactions. The increased microvascular density reflects compensatory restoration for disabled function. Most remarkable was the exaggerated secretory activity (also at luminal surfaces) underlining the regulatory key role of extracellular matrix protein 1 (ECM1; mutated in LP) in export or turnover of all major BM-components.
Journal: Journal of Dermatological Science - Volume 42, Issue 3, June 2006, Pages 231–239