COMPARATIVE ASPECTS OF SPLENIC MICROCIRCULATORY PATHWAYS IN MAMMALS -THE REGION BORDERING THE WHITE PULP

Citation
Ee. Schmidt et al., COMPARATIVE ASPECTS OF SPLENIC MICROCIRCULATORY PATHWAYS IN MAMMALS -THE REGION BORDERING THE WHITE PULP, Scanning microscopy, 7(2), 1993, pp. 613-628
Citations number
50
Categorie Soggetti
Microscopy
Journal title
ISSN journal
08917035
Volume
7
Issue
2
Year of publication
1993
Pages
613 - 628
Database
ISI
SICI code
0891-7035(1993)7:2<613:CAOSMP>2.0.ZU;2-T
Abstract
Splenic microcorrosion casts prepared using minimal volumes of materia l show that most of the flow passes through the region bordering the w hite pulp. However, the nature of these microcirculatory pathways has received little attention. We have studied these in dog, cat, rat, mou se, and normal versus diseased human spleens. In all 5 species, a marg inal sinus (MS) of anastomosing vascular spaces 5-10 mu m thick lies b etween the white pulp and marginal zone (MZ). The morphology differs b etween species and the MS is absent in immune thrombocytopenia. The MS fills by circumferential flow before blood passes outward to the MZ. Many capillaries supply the MS and MZ, their arrangement and degree of branching differing among species. Capillaries never terminate within the reticulum of the white pulp. In immune thrombocytopenia, marked v ascular hyperplasia occurs within white pulp and MZ. The perimarginal cavernous sinus plexus (PMCS), found in human, dog and rat, comprises large flattened spaces up to 300 mu m x 1000 mu m in area and 30-100 m u m thick. It lies between the MZ and red pulp or directly adjacent to white pulp, and receives flow principally via the MZ. In sinusal sple ens, the MS, MZ and PMCS are drained by open-ended venous sinuses. In non-sinusal spleens, the MS and MZ are drained by pulp venules. Approx imately 90% of the splenic inflow passes through the region bordering the white pulp, bypassing the filtration beds of the red pulp. This su ggests that immunologic functions of the spleen take precedence over t he filtration of blood cellular elements in the red pulp.