人糖尿病抑郁的自身抗体体外抑制成体神经祖细胞并诱导啮齿动物的抑郁样行为。

Journal of endocrinology and diabetes Pub Date : 2015-01-01 Epub Date: 2015-04-25 DOI:10.15226/2374-6890/2/2/00119
Mark B Zimering, Joseph A Behnke, Smita Thakker-Varia, Janet Alder
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摘要

目的:糖尿病抑郁增加与微血管并发症相关。我们检验了一种假设,即具有抗内皮和抗神经元特性的循环自身抗体在合并抑郁的糖尿病亚群中增加。方法:从20例糖尿病抑郁症患者和30例年龄匹配的对照组的血浆中提取蛋白a清液,检测其对内皮细胞存活、大鼠嗜铬细胞瘤(PC12)细胞的神经突生长或成年大鼠齿状回神经祖细胞的过程延伸和存活的影响。将抑郁或非抑郁糖尿病患者的蛋白a洗脱液(经脑室内途径)注射到小鼠体内,并在7-10天后进行行为测试(蔗糖偏好和悬尾测试),以确定自身抗体是否引起快感缺乏或绝望。结果:与对照组、糖尿病(n=20)或非糖尿病(n=10)无抑郁患者的自身抗体相比,糖尿病抑郁(n=20)自身抗体对PC12细胞神经突生长(P)或内皮细胞增殖有显著抑制作用。与糖尿病患者(n=12)和非糖尿病无抑郁患者(n=7)相比,糖尿病抑制自身抗体(5 ~ 7 μg/mL)显著降低成年大鼠齿状回神经祖细胞的过程延长和存活(P)。10微摩尔浓度的选择性rho相关蛋白激酶(ROCK)抑制剂Y27632可显著阻止糖尿病抑制自身抗体诱导的(P)神经祖细胞过程收缩(n=5)。用糖尿病抑郁自身抗体治疗的小鼠(n=16来自两名不同患者的自身抗体)比用糖尿病对照自身抗体治疗的小鼠(n=16来自两名不同患者的自身抗体)表现出显著降低(P=0.027)的蔗糖偏好(快感缺乏)。结论:这些数据表明,老年糖尿病抑郁症患者的自身抗体抑制内皮细胞的存活,并损害体外成人齿状回神经祖细胞的过程延伸和存活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Autoantibodies in Human Diabetic Depression Inhibit Adult Neural Progenitor Cells In vitro and Induce Depressive-Like Behavior in Rodents.

Aim: Diabetic depression increases in association with microvascular complications. We tested a hypothesis that circulating autoantibodies having anti-endothelial and anti-neuronal properties increase in subsets of diabetes with co-morbid depression.

Methods: Protein-A eluates from plasma of 20 diabetic depression patients and 30 age-matched controls were tested for effects on endothelial cell survival, neurite outgrowth in rat pheochromocytoma (PC12) cells, or process extension and survival in adult rat dentate gyrus neural progenitor cells. The protein-A eluates from depressed or non-depressed, diabetic patients were injected (via intracerebroventricular route) into mice and 7-10 days later behavioral tests (sucrose preference, and tail suspension tests) were conducted to determine whether the autoantibodies induced anhedonia or despair.

Results: Diabetic depression (n=20) autoantibodies caused a significant inhibition of PC12 cell neurite outgrowth (P<0.001) or endothelial cell proliferation compared to autoantibodies in control, diabetic (n=20) or non-diabetic (n=10) patients without depression. Process extension and survival in adult rat dentate gyrus neural progenitor cells was significantly reduced (P<0.001) by diabetic depression autoantibodies (n= 11) compared to the effects from similar concentrations (5-7 μg/mL) of autoantibodies in diabetic (n=12) or non-diabetic patients without depression (n=7). Ten micromolar concentrations of Y27632, a selective Rho-Associated Protein Kinase (ROCK) inhibitor, significantly prevented (P<0.0001) neural progenitor cell process retraction induced by diabetes depression autoantibodies (n=5). Mice treated with diabetic depression autoantibodies (n=16 from two different patients' autoantibodies) exhibited significantly reduced (P=0.027) sucrose preference (anhedonia) compared to mice treated with diabetic control autoantibodies (n=16 from two different patients' autoantibodies).

Conclusion: These data suggest that autoantibodies in a subset of older adult diabetic depression inhibit endothelial cell survival, and impair process extension and survival in adult dentate gyrus neural progenitor cells in vitro.

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