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Association of low numbers of CD 206‐positive cells with loss of ICC in the gastric body of patients with diabetic gastroparesis

机译:糖尿病性胃轻瘫患者胃体内CD206阳性细胞数量减少与ICC丢失的关系

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摘要

Background There is increasing evidence for specific cellular changes in the stomach of patients with diabetic ( DG ) and idiopathic ( IG ) gastroparesis. The most significant findings are loss of interstitial cells of Cajal ( ICC ), neuronal abnormalities, and an immune cellular infiltrate. Studies done in diabetic mice have shown a cytoprotective effect of CD 206+ M2 macrophages. To quantify overall immune cellular infiltrate, identify macrophage populations, and quantify CD 206+ and i NOS + cells. To investigate associations between cellular phenotypes and ICC . Methods Full thickness gastric body biopsies were obtained from non‐diabetic controls (C), diabetic controls ( DC ), DG , and IG patients. Sections were labeled for CD 45, CD 206, Kit, i NOS , and putative human macrophage markers ( HAM 56, CD 68, and EMR 1). Immunoreactive cells were quantified from the circular muscle layer. Key Results Significantly fewer ICC were detected in DG and IG tissues, but there were no differences in the numbers of cells immunoreactive for other markers between patient groups. There was a significant correlation between the number of CD 206+ cells and ICC in DG and DC patients, but not in C and IG and a significant correlation between i NOS + cells and ICC in the DC group, but not the other groups. CD 68 and HAM 56 reliably labeled the same cell populations, but EMR 1 labeled other cell types. Conclusions & Inferences Depletion of ICC and correlation with changes in CD 206+ cell numbers in DC and DG patients suggests that in humans, like mice, CD 206+ macrophages may play a cytoprotective role in diabetes. These findings may lead to novel therapeutic options, targeting alternatively activated macrophages. Loss of interstitial cells of Cajal and an immune cell infiltrate have been identified in the gastric smooth muscle of patients with gastroparesis. This study reports a correlation between ICC numbers and CD206‐positive, alternatively activated M2 macrophage numbers in the gastric body of patients with diabetes (Panels B, D), but not in non‐diabetic controls (A) or idiopathic gastroparesis (C). Thus, CD206‐positive macrophages may play a cytoprotective role in the stomach of diabetic patients.
机译:背景技术越来越多的证据表明患有糖尿病(DG)和特发性(IG)胃轻瘫的患者的胃中会发生特定的细胞变化。最重要的发现是Cajal(ICC)的间质细胞丢失,神经元异常和免疫细胞浸润。在糖尿病小鼠中进行的研究表明,CD 206+ M2巨噬细胞具有细胞保护作用。为了量化总体免疫细胞浸润,确定巨噬细胞种群,并量化CD 206+和i NOS +细胞。研究细胞表型与ICC之间的关联。方法从非糖尿病对照(C),糖尿病对照(DC),DG和IG患者获得胃全层活检。将切片标记为CD 45,CD 206,试剂盒,i NOS和假定的人类巨噬细胞标记(HAM 56,CD 68和EMR 1)。从环状肌层定量免疫反应性细胞。关键结果在DG和IG组织中检测到的ICC显着减少,但患者组之间对其他标志物具有免疫反应性的细胞数量没有差异。 DG和DC患者的CD 206 +细胞数量与ICC之间存在显着相关性,而C和IG患者之间无显着相关性,DC组中i NOS +细胞与ICC之间存在显着相关性,而其他组则无相关性。 CD 68和HAM 56可靠地标记了相同的细胞群,而EMR 1标记了其他细胞类型。结论和推断DC和DG患者的ICC耗竭及其与CD 206+细胞数量变化的相关性表明,在人类中,如小鼠一样,CD 206+巨噬细胞可能在糖尿病中发挥细胞保护作用。这些发现可能导致新的治疗选择,靶向交替激活的巨噬细胞。胃轻瘫患者的胃平滑肌中已发现Cajal间质细胞的丢失和免疫细胞的浸润。这项研究报告了糖​​尿病患者胃体中ICC数量与CD206阳性或交替激活的M2巨噬细胞数量之间的相关性(图B,D),但非糖尿病对照(A)或特发性胃轻瘫(C)则无此相关性。因此,CD206阳性巨噬细胞可能在糖尿病患者的胃中起细胞保护作用。

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