1973
DOI: 10.1002/aja.1001360303
|View full text |Cite
|
Sign up to set email alerts
|

The external glial limiting membrane in Macaca: Ultrastructure of a laminated glioepithelium

Abstract: The external glial limiting membrane in Macaca is a multilaminar epithelium-like mantle formed by the perikarya and interdigitating cell processes of astrocytes. It is separated from the overlying subarachnoid space by a typical basement membrane. Tonofilaments, about 100 in diameter, course through the cytoplasm of the processes in sheaths which run in different planes in successive layers of the mantle, forming a course brushwork. Beneath the surface plasma membrane of the superficial astrocytes is a filamen… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

1
7
0

Year Published

1975
1975
2011
2011

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations
Cited by 41 publications
(8 citation statements)
references
References 21 publications
1
7
0
Order By: Relevance
“…In the present study, the only long-distance-migrated CaBLir glial cells were observed in the torus lateralis hypothalami; these cells appear to have originated from the pretectal-tegmental ependyma, in agreement with the embryonic origin of this torus (Bergquist 1932;. These cells probably do not correspond to the marginal astrocytes found in reptiles and mammals (see Bondareff and McLone 1973;Braak 1975;Hajós and Kálmán 1989;Bodega et al 1990c), since their morphology and processes indicate that they should be classified as radial glia cells.…”
Section: Cabl Immunocytochemistry and Migrated Populations Of Glia Cellssupporting
confidence: 72%
“…In the present study, the only long-distance-migrated CaBLir glial cells were observed in the torus lateralis hypothalami; these cells appear to have originated from the pretectal-tegmental ependyma, in agreement with the embryonic origin of this torus (Bergquist 1932;. These cells probably do not correspond to the marginal astrocytes found in reptiles and mammals (see Bondareff and McLone 1973;Braak 1975;Hajós and Kálmán 1989;Bodega et al 1990c), since their morphology and processes indicate that they should be classified as radial glia cells.…”
Section: Cabl Immunocytochemistry and Migrated Populations Of Glia Cellssupporting
confidence: 72%
“…In mammals, the AQP4-rich astrocyte processes of the glia limitans interna and glia limitans externa form a dense mesh at the brain-CSF boundaries. Ultrastructural studies show that these long astrocytic processes are separated by narrow (<20 nm) intercellular clefts, are interconnected by gap junctions, and lack transcytotic vesicles (31)(32)(33). Because of the long diffusion path, the presence of gap junctions between adjacent astrocytes, and the absence of transcytotic transport between clefts, the glia limitans is a significant permeability barrier to the extracellular flow of water and solutes.…”
Section: Discussionmentioning
confidence: 99%
“…The glia limitans, however, is known to consist of overlapping astrocyte processes at the surface of the brain in regions such as visual cortex of cat (Haug, 1971;Williams, 1975), parieto-occipital cortex in macaca monkeys (Bondareff and McLone, 1973) and temporal lobe in humans (Braak, 1975). Ultrastructural examples of overlapping thin sheets of astrocyte processes are also known from the neuropil of medulla oblongata (Mugnaini and Walberg, 1964;Walberg, 1963) and olfactory bulb (Brightman, 2002;Reese and Brightman, 1965), and recently, in the habenula (Andres et al, 1999).…”
Section: Introductionmentioning
confidence: 99%