Grațiela Grădișteanu Pîrcălăbioru, M. Chifiriuc, R. Stoica
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引用次数: 0
摘要
微生物与宿主先天免疫系统的相互作用是可能改变糖尿病及其相关并发症的关键因素。最近的报道已经阐明了NLRP3炎症小体在糖尿病中的作用,但据我们所知,没有关于其他炎症小体在糖尿病诱导炎症中的作用的数据。为了研究这一点,我们采集了伴有肾病的2型糖尿病(T2DM)患者和健康志愿者的血液样本。红细胞裂解后,从所有采集的血液样本中分离RNA。采用实时荧光定量PCR (quantitative Real Time PCR, qRT-PCR)检测NLRP 6、NLRP3、ASC、PRO-IL1Β、PRO-IL18的表达。与健康对照组相比,糖尿病肾病患者NLRP3炎性体表达较高,而NLRP6炎性体表达无显著差异。此外,戊traxin 3在糖尿病肾病患者中表达升高。对患者临床资料的详细分析显示,在治疗方案中接受碳酸西维拉默治疗的患者中,戊traxin 3 (PTX3)和NLRP3相关基因的表达水平较低。
SEVELAMER CARBONATE MODULATES THE NLRP3 AND NLRP6 INFLAMMASOME EXPRESSION IN PATIENTS WITH DIABETIC NEPHROPATHY
Interaction of microorganisms with the host innate immune system is a crucial factor that could modify diabetes and its associated complications. Recent reports have elucidated the role of NLRP3 inflammasome in diabetes, but to our knowledge there is no data regarding the role of other inflammasomes in diabetes-induced inflammation. To investigate this, blood samples were collected from type 2 diabetes (T2DM) patients with nephropathy as well as from healthy volunteers. After red blood cell lysis, RNA was isolated from all collected blood samples. The expression of NLRP 6, NLRP3, ASC, PRO-IL1Β, and PRO-IL18 was assessed by quantitative Real Time PCR (qRT-PCR). Patients with diabetic nephropathy showed higher NLRP3 inflammasome expression compared to healthy controls whereas no significant differences were observed in case of NLRP6 inflammasome. In addition, Pentraxin 3 expression was elevated in patients with diabetic nephropathy. A detailed analysis of the patient’s clinical data revealed the fact that subjects receiving sevelamer carbonate in their treatment plan harboured low expression of Pentraxin 3 (PTX3) and NLRP3 associated genes.