血小板衍生生长因子受体-β在人腹膜中的表达。

Nephron Clinical Practice Pub Date : 2014-01-01 Epub Date: 2014-11-06 DOI:10.1159/000368241
Harald Seeger, Niko Braun, Joerg Latus, M Dominik Alscher, Peter Fritz, Ilka Edenhofer, Dagmar Biegger, Maja Lindenmeier, Rudolf P Wüthrich, Stephan Segerer
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引用次数: 7

摘要

简介:单纯性腹膜纤维化和包封性腹膜硬化(EPS)是腹膜透析(PD)患者腹膜的重要病变。我们以前曾在EPS患者的腹膜活检中描述过podoplanin阳性肌成纤维细胞群。血小板衍生生长因子受体-β (PDGFRβ)是周细胞的标志物,PDGFs可能参与腹膜的纤维化反应。本研究旨在描述PDGFRβ在人腹膜中的表达。方法:在回顾性分析中,我们将PDGFRβ定位于EPS患者(n = 6)和无EPS症状的PD患者(n = 5)的腹膜活检中,并将其与正常腹膜(n = 4)和尿毒症患者腹膜(n = 5)进行比较。连续切片进行平滑肌肌动蛋白(SMA)和足平面蛋白染色。2名对诊断不知情的观察者对载玻片进行半定量评分。结果:所有活检组织的动脉壁细胞均表达PDGFRβ。正常腹膜中存在大量pdgfr β阳性细胞,而连续切片显示SMA阴性。在PD患者中,大量PDGFRβ也呈SMA阳性。在EPS中,大多数podoplanin阳性细胞PDGFRβ阳性。在正常和尿毒症患者的腹膜活检中,SMA的表达主要局限于动脉壁细胞。Podoplanin的表达仅限于正常腹膜、尿毒症患者和无EPS的PD患者的淋巴管。结论:由于podoplanin阳性的肌成纤维细胞表达PDGFRβ,这些细胞可能与周细胞有关(而不是其他来源的成纤维细胞)。PDGFRβ可能成为EPS的治疗靶点。
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Platelet-derived growth factor receptor-β expression in human peritoneum.

Introduction: Simple peritoneal fibrosis and encapsulating peritoneal sclerosis (EPS) are important lesions in the peritoneum of patients on peritoneal dialysis (PD). We have previously described a population of podoplanin-positive myofibroblasts in peritoneal biopsies from patients with EPS. Platelet-derived growth factor receptor-β (PDGFRβ) is a marker of pericytes, and PDGFs might be involved in the fibrotic response of the peritoneum. This study aimed to describe PDGFRβ in the human peritoneum.

Methods: In this retrospective analysis, we localized PDGFRβ in peritoneal biopsies from patients with EPS (n = 6) and patients on PD without signs of EPS (n = 5), and compared them with normal peritoneum (n = 4) and peritoneum from uremic patients (n = 5). Consecutive sections were stained for smooth-muscle actin (SMA) and podoplanin. Slides were scored semiquantitatively by 2 observers blinded to the diagnosis.

Results: PDGFRβ was expressed by cells of arterial walls in all biopsies. A prominent population of PDGFRβ-positive cells was present in the normal peritoneum, which were SMA negative on consecutive sections. In patients on PD, a high number of PDGFRβ were also positive for SMA. In EPS, the majority of podoplanin-positive cells were positive for PDGFRβ. In peritoneal biopsies from normal and uremic patients, the expression of SMA was mainly restricted to cells of arterial walls. Podoplanin expression was restricted to lymphatic vessels in normal peritoneum, in uremic patients, and in patients on PD without EPS.

Conclusions: As podoplanin-positive myofibroblasts express PDGFRβ, these cells might be related to pericytes (rather than other sources of fibroblasts). PDGFRβ might turn out to be a therapeutic target in EPS.

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来源期刊
Nephron Clinical Practice
Nephron Clinical Practice 医学-泌尿学与肾脏学
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