女性糖尿病db/db模型中神经血管单元的超微结构重构——第三部分:少突胶质细胞和髓磷脂

M. Hayden, D. Grant, A. Aroor, V. DeMarco
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引用次数: 12

摘要

肥胖、胰岛素抵抗和2型糖尿病与糖尿病性心肌病有关。在这项研究中,我们检验了大脑皮层灰质和皮层灰质与白质之间更深的过渡区区域内的神经血管单位(NVU)、少突胶质细胞和髓鞘可能异常的假设。单基因(Leprdb)女性糖尿病患者db/db [BKS。采用CgDock7m +/+ Leprdb/J] (DBC)小鼠模型进行超微结构研究。在牺牲(20周龄)后,DBC和年龄匹配的非糖尿病野生型对照C57BL/KsJ (CKC)小鼠的左脑半球立即浸泡固定。我们发现少突胶质细胞有明显的重塑,核染色质凝聚和体积增加,过渡区细胞质中活跃的髓鞘形成位点数量增加。与CKC模型相比,DBC中有明显的髓鞘发育异常,表现为外髓鞘片鞘分裂、分离和球囊化,灰质中线粒体异常;与CKC模型相比,DBC中有类似的髓鞘重塑改变,表现为明显的紊乱,并伴有过渡带轴突塌陷。
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Ultrastructural Remodeling of the Neurovascular Unit in the Female Diabetic db/db Model—Part III: Oligodendrocyte and Myelin
Obesity, insulin resistance, and type 2 diabetes mellitus are associated with diabetic cognopathy. In this study, we tested the hypothesis that neurovascular unit(s) (NVU), oligodendrocytes, and myelin within cerebral cortical grey matter and deeper transitional zone regions between the cortical grey matter and white matter may be abnormal. The monogenic (Leprdb) female diabetic db/db [BKS.CgDock7m +/+ Leprdb/J] (DBC) mouse model was utilized for this ultrastructural study. Upon sacrifice (20 weeks of age), left-brain hemispheres of the DBC and age-matched non-diabetic wild type control C57BL/KsJ (CKC) mice were immediately immersion-fixed. We found prominent remodeling of oligodendrocytes with increased nuclear chromatin condensation and volume and increased numbers of active myelination sites of the cytoplasm in transition zones. Marked dysmyelination with outer myelin lamellae sheath splitting, separation, and ballooning with aberrant mitochondria in grey matter and similar myelin remodeling changes with marked disarray with additional axonal collapse in transitional zones in DBC as compared to CKC models.
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