Quantitative and ultrastructural changes in glia and pericytes in the parietal cortex of the aging rat

被引:0
|
作者
Peinado, MA
Quesada, A
Pedrosa, JA
Torres, MI
Martinez, M
Esteban, FJ
Del Moral, M
Hernandez, R
Rodrigo, J
Peinado, JM
机构
[1] Univ Jaen, Dept Cell Biol, Sch Expt Sci, E-23071 Jaen, Spain
[2] CSIC, Inst Cajal, E-28002 Madrid, Spain
[3] Univ Granada, Dept Biochem, F Oloriz Inst Neurosci, E-18071 Granada, Spain
关键词
astrocytes; oligodendrocytes; microglia; pericytes; parietal cortex; aging; rat;
D O I
10.1002/(SICI)1097-0029(19981001)43:1<34::AID-JEMT6>3.0.CO;2-G
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
The frequency of astrocytes, microglia plus oligodendrocytes, and pericytes displaying nuclei was analyzed and quantified in 160-mu m-wide strips of the parietal cortex (Par1 region) from young and aged Wistar rats. The study was performed on two groups of rats aged 3-4 and 32-36 months. Quantifications of the glial cell types and pericytes were made in 1-mu m-thick sections stained with toluidine blue. Ultrathin sections were also made to analyze the ultrastructural features of these cells during aging. Astrocytes and pericytes increased in number by about 20% and 22%, respectively, with age. These increases were most significant in layers II-IV and V for both cellular types. Clusters of astrocytes were common in these layers of aging rats. The ultrastructural analysis also indicated changes in all cell types that stored inclusions and vacuoles with age, which were particularly abundant in microglial cells. End-feet astrocytes and pericytes surrounding the vascular wall also contained vacuoles and inclusions, and consequently the vascular wall increased in thickness. In conclusion, the aging process increased astrocyte and pericyte populations, but not microglia plus oligodendrocyte populations, in the rat parietal cortex. Although no significant change in nuclear size could be observed in any cell type, all glial cells as well as pericytes underwent morphological ultrastructural changes. These modifications may result from the need to correct possible homeostatic imbalances during aging. (C) 1998 Wiley-Liss, Inc.
引用
收藏
页码:34 / 42
页数:9
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