在人类 2 型糖尿病中,血管生成素样蛋白 4 的循环和组织特异性转录。
Circulating and tissue specific transcription of angiopoietin-like protein 4 in human Type 2 diabetes.
机构信息
Diabetes and Obesity Research Group, Institute of Biological and Clinical Sciences, University of Exeter, EX2 5DW, United Kingdom of Great Britain and Northern Ireland.
Exeter NIHR Clinical Research Facility, RILD, Exeter EX2 5DW, United Kingdom of Great Britain and Northern Ireland.
出版信息
Metabolism. 2020 May;106:154192. doi: 10.1016/j.metabol.2020.154192. Epub 2020 Feb 26.
AIMS
Obesity is associated with adipose tissue (AT) dysfunction marked by cellular hypertrophy, inflammation, hypoxia and fibrosis. Angiopoietin-like protein 4 (ANGPTL4) inhibits lipoprotein lipase which regulates triglyceride storage. Recently, inhibition of ANGPTL4 has been suggested as potential treatment for type 2 diabetes. Here we evaluate ANGPTL4's role in diabetes and examine ANGPTL4 in relation to markers of AT dysfunction and fatty liver disease.
MATERIALS & METHODS: We obtained a unique set of paired samples from subjects undergoing weight loss surgery including subcutaneous AT (SCAT), omental AT (OMAT), liver, thigh muscle biopsies and serum including a post-surgical SCAT biopsy after 9 months.
RESULTS
SCAT ANGPTL4 expression and circulating protein levels were higher in people with diabetes and correlated with glucose levels and HOMA-IR but not BMI. At post-surgical follow up, SCAT ANGPTL4 declined in subjects with diabetes to levels of those without diabetes. ANGPTL4 expression correlated with HIF1A and inflammation (MCP-1, IL-6).
CONCLUSIONS
We found that SCAT ANGPTL4 was closely linked with the expression of ANGPTL4 in the liver and represented a good proxy for liver steatosis. We suggest the elevation of ANGPTL4 levels in diabetes and the association with inflammation and hypoxia is due to a compensatory mechanism to limit further AT dysfunction. A reduction of ANGPTL4 for the treatment of T2DM as previously suggested is thus unlikely to be of further benefit.
目的
肥胖与脂肪组织(AT)功能障碍有关,其特征为细胞肥大、炎症、缺氧和纤维化。血管生成素样蛋白 4(ANGPTL4)抑制脂蛋白脂肪酶,后者调节甘油三酯储存。最近,抑制 ANGPTL4 被认为是治疗 2 型糖尿病的潜在方法。本研究评估了 ANGPTL4 在糖尿病中的作用,并研究了 ANGPTL4 与 AT 功能障碍和脂肪肝疾病标志物的关系。
材料与方法
我们从接受减肥手术的患者中获得了一组独特的配对样本,包括皮下脂肪组织(SCAT)、网膜脂肪组织(OMAT)、肝脏、大腿肌肉活检和血清,包括手术后 9 个月的 SCAT 活检。
结果
糖尿病患者的 SCAT ANGPTL4 表达和循环蛋白水平较高,与血糖水平和 HOMA-IR 相关,但与 BMI 无关。在手术后的随访中,糖尿病患者的 SCAT ANGPTL4 下降至非糖尿病患者的水平。ANGPTL4 表达与 HIF1A 和炎症(MCP-1、IL-6)相关。
结论
我们发现 SCAT ANGPTL4 与肝脏中 ANGPTL4 的表达密切相关,是肝脂肪变性的良好替代标志物。我们认为,糖尿病中 ANGPTL4 水平升高及其与炎症和缺氧的关联是由于一种补偿机制,以限制进一步的 AT 功能障碍。因此,如前所述,降低 ANGPTL4 以治疗 2 型糖尿病不太可能进一步获益。