Literature DB >> 2353135

Hypoxia/reoxygenation injury in liver: Kupffer cells are much more vulnerable to reoxygenation than to hypoxia.

B Rymsa1, H D Becker, W Lauchart, H de Groot.   

Abstract

Cell injury due to hypoxia and reoxygenation was studied in primary cultured rat Kupffer cells. Under hypoxic conditions only 20% of the cells had lost their viability after 12 h of incubation. In contrast, almost complete losses of cell viability were observed when reoxygenation was performed after 2, 4 or 6 h of hypoxia. The time-course of reoxygenation injury in Kupffer cells was characterized by a lag phase of 2 h during which no difference between reoxygenated and hypoxically incubated cells was apparent; during the next 4 h, there was an increase of up to 100% in the amount of nonviable cells in the reoxygenated cultures. These results indicate that Kupffer cells were much more vulnerable to reoxygenation than to hypoxia. The time-course of cell damage upon hypoxia/reoxygenation may indicate a self-destruction mechanism caused by an oxygen-triggered activation of these cells.

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Year:  1990        PMID: 2353135

Source DB:  PubMed          Journal:  Res Commun Chem Pathol Pharmacol        ISSN: 0034-5164


  4 in total

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3.  Rapid conversion to high xanthine oxidase activity in viable Kupffer cells during hypoxia.

Authors:  J S Wiezorek; D H Brown; D E Kupperman; C A Brass
Journal:  J Clin Invest       Date:  1994-12       Impact factor: 14.808

4.  Hypoxia enhances the proliferative response of macrophages to CSF-1 and their pro-survival response to TNF.

Authors:  John A Hamilton; Derek C Lacey; Amanda Turner; Bernard de Kok; Jennifer Huynh; Glen M Scholz
Journal:  PLoS One       Date:  2012-09-19       Impact factor: 3.240

  4 in total

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