| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
(Stroke. 2007;38:2577.)
© 2007 American Heart Association, Inc.
Original Contributions |
From the Department of Neuropathology, Tokyo Metropolitan Institute for Neuroscience, Tokyo, Japan.
Correspondence to Umeo Ito, MD, PhD, FAHA, Department of Neuropathology, Tokyo Metropolitan Institute for Neuroscience, Tokyo, 2-6, Musashidai, Fuchu-shi, Tokyo 183-8526, Japan. E-mail umeo-ito{at}nn.iij4u.or.jp
Background and Purpose— Because the mechanism for scavenging acidophilic electron-dense dead neurons disseminated among the neuritic networks of surviving neurons in the ischemic penumbra of the cerebral cortex is still obscure, we investigated the fate of them up to 24 weeks after the ischemic insult.
Methods— Stroke-positive animals were selected according to their stroke index score during the first 10-minute left carotid occlusion done twice with a 5-hour interval. The animals were killed at various times after the second ischemic insult. Ultrathin sections including the second through fourth cortical layers were obtained from the neocortex coronally sectioned at the infundibular level in which the penumbra appeared and was observed by electron microscopy. We determined the percentages of resting, activated, and phagocytic microglia and astrocytes in the specimens obtained at various times postischemia.
Results— The electron-dense neurons had been fragmented into granular pieces by invading astrocytic processes from the periphery of the dead neurons and only the central portion remained. These granular pieces were dispersed along the extracellular spaces in the neuropil. By 8 to 24 weeks, the central core portion became a tiny vesicular particle (3.5 to 5.5 µm in diameter) with a central dot. Microglia and astrocytes phagocytized these dispersed granular pieces.
Conclusions— We found a novel scavenger mechanism in the ischemic penumbra, one by which dead neurons were fragmented by invading small astrocytic processes and only a thinned-out core portion remained, which finally became a tiny vesicular particle. The dispersed fragmented pieces were phagocytized by the microglia and astrocytes late, at 8 to 24 weeks postischemia.
Key Words: cortical ischemic penumbra phagocytosis scavenging of dead neurons transient cerebral ischemia
This article has been cited by other articles:
![]() |
U. Ito, Y. Hakamata, E. Kawakami, and K. Oyanagi Degeneration of Astrocytic Processes and Their Mitochondria in Cerebral Cortical Regions Peripheral to the Cortical Infarction: Heterogeneity of Their Disintegration Is Closely Associated With Disseminated Selective Neuronal Necrosis and Maturation of Injury Stroke, June 1, 2009; 40(6): 2173 - 2181. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Kimura, T. Ohmori, Y. Kashiwakura, R. Ohkawa, S. Madoiwa, J. Mimuro, K. Shimazaki, Y. Hoshino, Y. Yatomi, and Y. Sakata Antagonism of Sphingosine 1-Phosphate Receptor-2 Enhances Migration of Neural Progenitor Cells Toward an Area of Brain Infarction * Supplemental Materials and Methods Stroke, December 1, 2008; 39(12): 3411 - 3417. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. V. Guadagno, P. S. Jones, F. I. Aigbirhio, D. Wang, T. D. Fryer, D. J. Day, N. Antoun, I. Nimmo-Smith, E. A. Warburton, and J. C. Baron Selective neuronal loss in rescued penumbra relates to initial hypoperfusion Brain, October 1, 2008; 131(10): 2666 - 2678. [Abstract] [Full Text] [PDF] |
||||
|
Stroke Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 2007 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |