V. Neaud et al., ULTRASTRUCTURE OF HUMAN KUPFFER CELLS MAINTAINED IN CULTURE, Journal of submicroscopic cytology and pathology, 27(2), 1995, pp. 161-170
Sinusoidal cells were isolated by collagenase perfusion and metrizamid
e gradient centrifugation, from liver resected for partial hepatectomy
performed under warm ischemic conditions. Kupffer cells were then sep
arated from this population by centrifugal elutriation. Isolated Kupff
er cells showed good viability, with the typical features of Kupffer c
ells and were engaged in the endocytosis of foreign particles. They sh
owed numerous morphological criteria of activation. However, cultured
Kupffer cells were no long er in an activated state. Kupffer cells wer
e preserved in maintenance cultures for 2 weeks. Purity of these cultu
res was to 93-97% During culture, Kupffer cells retained their ultrast
ructural characteristics and were active in the endocytosis of latex b
eads and opsonized zymosan particles. It is thus possible that partial
hepatectomy performed under warm ischemia could provide valuable mate
rial for the study of Kupffer cells in vitro.