Kang Hsu Lin, Szász András, Valkusz Zsuzsanna, Várkonyi Tamás, Pósa Anikó, Kupai Krisztina
Department of Oral Biology and Experimental Dental Research, Faculty of Dentistry, University of Szeged, 6703 Szeged, Hungary.
Department of Internal Medicine, Albert Szent-Györgyi Medical School, University of Szeged, 6703 Szeged, Hungary.
Int J Mol Sci. 2025 Jun 25;26(13):6113. doi: 10.3390/ijms26136113.
Peptidylarginine deiminase 4 (PAD4) catalyzes protein citrullination, a post-translational modification implicated in type 1 diabetes mellitus (T1DM). This study examined PAD4 expression and activity in the pancreas of streptozotocin (STZ)-induced diabetic Wistar rats. Animals were divided into three groups: (A) STZ-induced diabetic rats (60 mg/kg, i.p.), (B) non-diabetic controls, and (C) diabetic rats treated with Cl-amidine (5 mg/kg), a pan-PAD inhibitor, from week six post-induction. Analyses included PAD4 mRNA and protein expression, citrullinated histone H3 (CitH3), calcium concentration, and neutrophil elastase activity. Diabetic rats exhibited increased PAD4 expression, CitH3 levels, and NETosis markers, alongside reduced pancreatic calcium, suggesting calcium consumption during PAD4 activation. Cl-amidine treatment attenuated NETosis. These results implicate PAD4 in T1DM pathogenesis via NETosis and support the utility of STZ-induced diabetic rats as a model for PAD4-targeted studies. Cl-amidine may represent a promising therapeutic approach to reduce pancreatic inflammation in T1DM.
肽基精氨酸脱亚氨酶4(PAD4)催化蛋白质瓜氨酸化,这是一种与1型糖尿病(T1DM)相关的翻译后修饰。本研究检测了链脲佐菌素(STZ)诱导的糖尿病Wistar大鼠胰腺中PAD4的表达和活性。动物被分为三组:(A)STZ诱导的糖尿病大鼠(60mg/kg,腹腔注射),(B)非糖尿病对照组,以及(C)诱导后第六周开始用泛PAD抑制剂氯脒(5mg/kg)治疗的糖尿病大鼠。分析包括PAD4 mRNA和蛋白表达、瓜氨酸化组蛋白H3(CitH3)、钙浓度和中性粒细胞弹性蛋白酶活性。糖尿病大鼠表现出PAD4表达增加、CitH3水平升高和NETosis标志物增加,同时胰腺钙减少,提示PAD4激活过程中钙的消耗。氯脒治疗减弱了NETosis。这些结果表明PAD4通过NETosis参与T1DM发病机制,并支持将STZ诱导的糖尿病大鼠作为PAD4靶向研究的模型。氯脒可能是一种有前景的治疗方法,可减轻T1DM中的胰腺炎症。