Pre-apoptotic alterations in hepatocytes of TNFalpha-treated galactosamine-sensitized mice.
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Pre-apoptotic alterations in hepatocytes of TNFalpha-treated galactosamine-sensitized mice. / Angermüller, S; Künstle, G; Tiegs, Gisa.
In: J HISTOCHEM CYTOCHEM, Vol. 46, No. 10, 10, 1998, p. 1175-1183.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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TY - JOUR
T1 - Pre-apoptotic alterations in hepatocytes of TNFalpha-treated galactosamine-sensitized mice.
AU - Angermüller, S
AU - Künstle, G
AU - Tiegs, Gisa
PY - 1998
Y1 - 1998
N2 - Tumor necrosis factor (TNF) induces apoptotic death of hepatocytes in the galactosamine (GalN)-sensitized mouse liver after 5 hr. In our study, the most remarkable sign of the early stage of apoptosis was the focal rupture of the outer mitochondrial membrane. Parts of the inner membrane extended through the gap of the outer membrane, whereas the rest of the inner membrane still formed the cristae. This feature appeared in hepatocytes before chromatin condensation. With the diaminobenzidine technique for localization of cytochrome oxidase activity, the reaction product was detectable by light and electron microscopy. Ten percent of the hepatocytes were apoptotic, with condensed chromatin and high enzyme activity, 37% were pre-apoptotic, without chromatin condensation but high enzyme activity, and 53% had neither condensed chromatin nor a remarkable reaction product of cytochrome oxidase activity. Fas (APO-1, CD95) molecules on the plasma membrane of hepatocytes increased and were represented immunohistochemically in cells without chromatin condensation. DNA strand breaks were also detectable before chromatin aggregation. The results of this study indicate that mitochondria play a pivotal role in pre-apoptotic hepatocytes, together with an increase of the Fas molecule on the plasma membrane and with the occurrence of DNA strand breaks in the nucleus.
AB - Tumor necrosis factor (TNF) induces apoptotic death of hepatocytes in the galactosamine (GalN)-sensitized mouse liver after 5 hr. In our study, the most remarkable sign of the early stage of apoptosis was the focal rupture of the outer mitochondrial membrane. Parts of the inner membrane extended through the gap of the outer membrane, whereas the rest of the inner membrane still formed the cristae. This feature appeared in hepatocytes before chromatin condensation. With the diaminobenzidine technique for localization of cytochrome oxidase activity, the reaction product was detectable by light and electron microscopy. Ten percent of the hepatocytes were apoptotic, with condensed chromatin and high enzyme activity, 37% were pre-apoptotic, without chromatin condensation but high enzyme activity, and 53% had neither condensed chromatin nor a remarkable reaction product of cytochrome oxidase activity. Fas (APO-1, CD95) molecules on the plasma membrane of hepatocytes increased and were represented immunohistochemically in cells without chromatin condensation. DNA strand breaks were also detectable before chromatin aggregation. The results of this study indicate that mitochondria play a pivotal role in pre-apoptotic hepatocytes, together with an increase of the Fas molecule on the plasma membrane and with the occurrence of DNA strand breaks in the nucleus.
KW - Animals
KW - Male
KW - Immunohistochemistry
KW - Mice
KW - Mice, Inbred BALB C
KW - Apoptosis
KW - Histocytochemistry
KW - Galactosamine/pharmacology
KW - DNA Fragmentation
KW - Tumor Necrosis Factor-alpha/pharmacology
KW - Antigens, CD95/analysis
KW - Chromatin/pathology
KW - Electron Transport Complex IV/analysis
KW - Liver/chemistry/drug effects/pathology/ultrastructure
KW - Mitochondria/pathology
KW - Animals
KW - Male
KW - Immunohistochemistry
KW - Mice
KW - Mice, Inbred BALB C
KW - Apoptosis
KW - Histocytochemistry
KW - Galactosamine/pharmacology
KW - DNA Fragmentation
KW - Tumor Necrosis Factor-alpha/pharmacology
KW - Antigens, CD95/analysis
KW - Chromatin/pathology
KW - Electron Transport Complex IV/analysis
KW - Liver/chemistry/drug effects/pathology/ultrastructure
KW - Mitochondria/pathology
M3 - SCORING: Journal article
VL - 46
SP - 1175
EP - 1183
JO - J HISTOCHEM CYTOCHEM
JF - J HISTOCHEM CYTOCHEM
SN - 0022-1554
IS - 10
M1 - 10
ER -