Membranous ultrastructure of human arachnoid cells

被引:21
作者
Hasegawa, M
Yamashima, T
Kida, S
Yamashita, J
机构
[1] Department of Neurosurgery, Kanazawa University, School of Medicine, Kanazawa
[2] Department of Neurosurgery, Kanazawa University, School of Medicine, Kanazawa, 920
关键词
CSF drainage; freeze-fracture; gap junction; human arachnoid granulation; micropinocytotic vesicle;
D O I
10.1097/00005072-199711000-00006
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The ultrastructure of arachnoid cell membranes was investigated by conventional transmission EM and by freeze-fracture techniques in human arachnoid granulations. Arachnoid cells showed widespread membrane specialization in the granulations including the formation of desmosome, gap junctions, tight junctions, intermediate junctions, hemidesmosome-like structures, and micropinocytotic vesicles. However, the extent of the specialization varied from portion to portion; this was clearly shown on freeze-fracture replicas. Numerous extracellular cisterns were separated by cytoplasmic bodies or slender processes, joined by these junctional complexes. Uncoated and coated vesicles were abundant along the surface of extracellular cisterns representing the pathway of CSE Complexes of branching tight junctions were comprised of 1-50 particle strands, which formed elaborate meshworks accompanied by numerous gap junctions and desmosomes. Micropinocytotic vesicles were often concentrated in the arachnoid cell cluster up to 40 per mu m(2), which is equivalent to the concentration in brain capillary endothelial cells. The results of this study clearly suggest that arachnoid cells in arachnoid granulations are not only tightly adherent to form a firm structure for the passage of CSE but that the arachnoid cells lining the CSF pathway show intense cell-cell communication and pinocytotic activity. This high transcellular activity probably reflects active transports or secretion of certain molecules by arachnoid cells.
引用
收藏
页码:1217 / 1227
页数:11
相关论文
共 66 条
[1]  
AGRE P, 1993, AM J PHYSIOL, V265, P463
[2]  
AKAI K, 1987, ACTA PATHOL JAPON, V37, P97
[3]  
ANGELOV DN, 1989, CELL TISSUE RES, V257, P207
[4]   PHYSIOLOGY OF ELECTROTONIC JUNCTIONS [J].
BENNETT, MVL .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1966, 137 (A2) :509-&
[5]  
Bradbury MW, 1981, AM J PHYSL REN FLUID, V9, P329, DOI DOI 10.1152/AJPRENAL.1981.240.4.F329
[7]   OVEREXPRESSION OF THE VIMENTIN GENE IN TRANSGENIC MICE INHIBITS NORMAL LENS CELL-DIFFERENTIATION [J].
CAPETANAKI, Y ;
SMITH, S ;
HEATH, JP .
JOURNAL OF CELL BIOLOGY, 1989, 109 (04) :1653-1664
[8]   AN ELECTRON MICROSCOPIC STUDY OF MENINGIOMAS [J].
CERVOSNAVARRO, J ;
VAZQUEZ, JJ .
ACTA NEUROPATHOLOGICA, 1969, 13 (04) :301-+
[9]   FRACTURE FACES OF ZONULAE OCCLUDENTES FROM TIGHT AND LEAKY EPITHELIA [J].
CLAUDE, P ;
GOODENOUGH, DA .
JOURNAL OF CELL BIOLOGY, 1973, 58 (02) :390-400
[10]  
CSERR HF, 1981, AM J PHYSIOL, V240, P319