Mechanism of Transport Through the Lymphatic Capillary Wall

1988 ◽  
pp. 100-100
Author(s):  
Judit Daróczy
1968 ◽  
Vol 36 (1) ◽  
pp. 129-149 ◽  
Author(s):  
L. V. Leak ◽  
J. F. Burke

The fine structure of the lymphatic capillary and the surrounding tissue areas was investigated. Instead of a continuous basal lamina (basement membrane) surrounding the capillary wall, these observations revealed the occurrence of numerous fine filaments that insert on the outer leaflet of the trilaminar unit membrane of the lymphatic endothelium. These filaments appear as individual units, or they are aggregated into bundles that are disposed parallel to the long axis of the lymphatic capillary wall and extend for long distances into the adjoining connective tissue area among the collagen fibers and connective tissue cells. The filaments measure about 100 A in width and have a hollow profile. They exhibit an irregular beaded pattern along their long axis and are densely stained with uranyl and lead. These filaments are similar to the microfibrils of the extracellular space and the filaments observed in the peripheral mantle of the elastic fibers. Infrequently, connections between these various elements are observed, suggesting that the lymphatic anchoring filaments may also contribute to the filamentous units of the extracellular space. It is suggested that these lymphatic anchoring filaments connect the small lymphatics to the surrounding tissues and represent the binding mechansim that is responsible for maintaining the firm attachment of the lymphatic capillary wall to the adjoining collagen fibers and cells of the connective tissue area.


2021 ◽  
Vol 9 (4) ◽  
pp. 31-37
Author(s):  
A. D. Kashin ◽  
I. D. Dimov ◽  
M. A. Zdorikova ◽  
I. S. Sesorova ◽  
N. R. Karelina ◽  
...  

The article highlights a complex of interendothelial connections of the lymphatic capillary of the rat intestinal villi, and focuses on the path of chylomicron transport through the lymphatic capillary wall after lipid loading.Material and methods. An experimental model was used to exclude a high lipid load; chymus from do- nor rats was injected with a syringe into the initial section of the small intestine in 10 Wistar rats. Chymus was collected from the initial section of the small intestine of donor animals 60 min after oral administration of 1.5 ml of corn oil. The control group consisted of the animals exposed to 12-hour fasting. The material was studied using transmission electron microscopy.Results. It was shown that most often cells are connected by tile-like (66±2.2%) or simple finger-like (27±2.4%) contacts, reinforced with a tight connection and a point adhesive (at the extreme point of contact). An- chor filaments located on the basal surface of endothelial cells at some distance from the extreme contact point “fixed” the lymphatic capillary wall, ensuring its stretching, changing the pressure inside the capillary and opening the valve. Under low lipid load, the main transport pathway of lipids from the interstitium of the intestinal villus to the lumen of the lymphatic capillary was through adhesive intercellular contacts. No chylomicrons were found in the lumen of plasmolemmal vesicles and kidneys. Caveolae in the endothelial cells of the lymphatic capillary, both after lipid loading and in hungry animals, were few. Caveolosomes were rare in both groups. Under low lipid load, no fusion of vesicles with the formation of transendothelial canals was found.Conclusions. The detected structure of contacts of the lymphatic capillary endothelium morphologically substantiates the hypothesis of the regulated resorption of interstitial fluid and macromolecules into the lumen of the lymphatic capillary.


Author(s):  
L. V. Leak ◽  
J. F. Burke

The vital role played by the lymphatic capillaries in the transfer of tissue fluids and particulate materials from the connective tissue area can be demonstrated by the rapid removal of injected vital dyes into the tissue areas. In order to ascertain the mechanisms involved in the transfer of substances from the connective tissue area at the ultrastructural level, we have injected colloidal particles of varying sizes which range from 80 A up to 900-mμ. These colloidal particles (colloidal ferritin 80-100A, thorium dioxide 100-200 A, biological carbon 200-300 and latex spheres 900-mμ) are injected directly into the interstitial spaces of the connective tissue with glass micro-needles mounted in a modified Chambers micromanipulator. The progress of the particles from the interstitial space into the lymphatic capillary lumen is followed by observing tissues from animals (skin of the guinea pig ear) that were injected at various time intervals ranging from 5 minutes up to 6 months.


1972 ◽  
Vol 68 (2_Supplb) ◽  
pp. S95-S111 ◽  
Author(s):  
Niels A. Lassen ◽  
Ole Andrée Larsen

ABSTRACT Indicators which freely cross the capillary wall can be used for measurement of tissue blood flow in many different ways. Basically one can distinguish two categories of methods, viz. the ones where the indicator enters the tissue via the inflowing blood and the ones where the indicator is deposited locally in the tissue. The most important methods are briefly described with special emphasis on the theory of blood flow measurement.


1994 ◽  
Vol 26 (12) ◽  
pp. 1635-1647 ◽  
Author(s):  
Frans A. Van Nieuwenhoven ◽  
Cees P.H.J. Verstijnen ◽  
Guillaume J.J.M. Van Eys ◽  
Eric Van Breda ◽  
Yvonne F. De Jong ◽  
...  

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