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DOI 10.3389/fneur.2018.00581

Медицинская библиотека · Frontiers in neurology · 2018

Ultrastructural Characteristics of Neuronal Death and White Matter Injury in Mouse Brain Tissues After Intracerebral Hemorrhage: Coexistence of Ferroptosis, Autophagy, and Necrosis.

Li Qian, Weiland Abigail, Chen Xuemei, Lan Xi, Han Xiaoning, Durham Frederick, Liu Xi, Wan Jieru, Ziai Wendy C, Hanley Daniel F, Wang Jian

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Аннотация

Although intracerebral hemorrhage (ICH) is a devastating disease worldwide, the pathologic changes in ultrastructure during the acute and chronic phases of ICH are poorly described. In this study, transmission electron microscopy was used to examine the ultrastructure of ICH-induced pathology. ICH was induced in mice by an intrastriatal injection of collagenase. Pathologic changes were observed in the acute (3 days), subacute (6 days), and chronic (28 days) phases. Compared with sham animals, we observed various types of cell death in the injured striatum during the acute phase of ICH, including necrosis, ferroptosis, and autophagy. Different degrees of axon degeneration in the striatum were seen in the acute phase, and axonal demyelination was observed in the ipsilateral striatum and corpus callosum at late time points. In addition, phagocytes, resident microglia, and infiltrating monocyte-macrophages were present around red blood cells and degenerating neurons and were observed to engulf red blood cells and other debris. Many synapses appeared abnormal or were lost. This systematic analysis of the pathologic changes in ultrastructure after ICH in mice provides information that will be valuable for future ICH pathology studies.

Для цитирования: Li Qian, Weiland Abigail, Chen Xuemei, Lan Xi, Han Xiaoning, Durham Frederick, Liu Xi, Wan Jieru, Ziai Wendy C, Hanley Daniel F, Wang Jian. Ultrastructural Characteristics of Neuronal Death and White Matter Injury in Mouse Brain Tissues After Intracerebral Hemorrhage: Coexistence of Ferroptosis, Autophagy, and Necrosis.. Frontiers in neurology. 2018. DOI: 10.3389/fneur.2018.00581.
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