Abstract
The liver is not only a metabolic organ, but it is also an organ of great immunological function (Thomas et al., 1973; Bradfield, 1974; Triger, 1976). Gates et al. (1961) determined that only 78.8 to 84.2% of total liver cells are represented by hepatocytes and 14.7 to 16.6% by littoral cells including Kupffer cells. It is estimated that approximately 90% of total phagocytic capacity of the RES is provided by the liver (van Furth, 1970). These facts suggest that in liver and other gastrointestinal diseases RE function may become altered, a situation that may have harmful consequences for the organism (Liehr, 1982). Alternatively, it has to be clarified whether a functionally and/or anatomically altered liver RE system contributes to the liver pathology itself or even is the reason that liver injury develops.
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Liehr, H. (1985). RES Function in Experimental and Human Liver Disease. In: Friedman, H., Escobar, M., Reichard, S.M., Filkins, J.P. (eds) The Reticuloendothelial System. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-2353-2_9
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