Temperature dependence of protein transport across lymphatic endothelium in vitro.
Open Access
- 1 February 1984
- journal article
- research article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 98 (2) , 629-640
- https://doi.org/10.1083/jcb.98.2.629
Abstract
The purpose of the work was to develop an in vitro model for the study of lymphatic endothelium and to determine, using this model, whether or not a cytoplasmic process may be involved in transendothelial transport. Segments of canine renal hilar lymphatics were dissected clean, cannulated at both ends, and transferred to a perfusion chamber for measurement of transendothelial protein transport and for ultrastructural tracer studies. The segments were subsequently processed for light microscopy and EM. By both structural and functional criteria the lymphatics were judged to have retained their integrity. At 37.degree. C, 36 lymphatics showed a mean rate of protein transport of 3.51 .+-. 0.45 (SEM [standard error of the mean]) .mu.g/min per cm2 of lymphatic endothelium. The rate was influenced by the temperature of the system, being significantly reduced by 49% .+-. 4.8, 31% .+-. 5.3 and 29% .+-. 3.9 when the temperature was lowered to 4.degree., 24.degree. and 30.degree. C, respectively. When the temperature was raised to 40.degree. C, the rate was significantly increased by 48% .+-. 12.2. The vesicular system and the intercellular regions in vessels with increased or reduced rates of transport were analyzed quantitatively to ascertain whether the rate changes could be correlated with ultrastructurally demonstrable changes in either of these postulated pathways. No significant changes in junctional or vesicular parameters were found between the control lymphatics and those perfused at 24.degree., 30.degree. and 40.degree. C. At 4.degree. C, the temperature at which the rate of protein transport was maximally reduced, vesicular size decreased and the number of free cytoplasmic vesicles increased, whereas the number associated with the abluminal and luminal surfaces decreased. It is concluded that isolated perfused lymphatic segments transport protein at a relatively constant rate under control conditions, and that this transendothelial transport comprises both temperature-dependent and temperature-independent mechanisms. The findings were considered in terms of the different theories of lymph formation and were interpreted as providing support for the vesiclar theory.This publication has 34 references indexed in Scilit:
- Heart microvessels: Presence of adenylate cyclase stimulated by catecholamines, prostaglandins, and adenosineMicrovascular Research, 1983
- Endocytosis and exocytosis of transferrin by isolated capillary endotheliumMicrovascular Research, 1983
- The organization of endocytotic vesicles in lymphatic endotheliumMicrovascular Research, 1983
- An ultrastructural study of the transport pathways across arcuate, interlobar, hilar, and capsular lymphatics in the dog kidneyMicrovascular Research, 1981
- Transport of protein across lymphatic endothelium in the rat kidneyMicrovascular Research, 1981
- Time dependent theory for vesicular transport across vascular endotheliumJournal of Theoretical Biology, 1980
- Renal lymphatic ultrastructure and translymphatic transportMicrovascular Research, 1980
- Metabolic studies on the micropinocytic process in endothelial cellsMicrovascular Research, 1979
- A theoretical model of the pinocytotic vesicular transport process in endothelial cellsJournal of Theoretical Biology, 1977
- Intestinal mucosal lymphatic permeability: An electron microscopic study of endothelial vesicles and cell junctionsJournal of Ultrastructure Research, 1970