Contribution of the mitochondrial compartment to the optical properties of the rat liver: a theoretical and practical approach

B Beauvoit, T Kitai, B Chance, B Beauvoit, T Kitai, B Chance

Abstract

The purpose of this work was to analyze the contribution of the mitochondria to the optical properties, i.e., light absorption and scattering, of the blood-free rat liver. Firstly, a theoretical model of the reduced scattering coefficient of the liver was performed by using the Mie theory, the Rayleigh-Debye-Gans approximation, and the electron microscopy descriptions of the liver ultrastructure. Compared with the hepatocyte volume, the nucleus and the peroxisomes, the mitochondria compartment, accounting for 22% of the liver cell volume, seemed to be the predominant factor for the light scattering of the liver. Second, by using time-resolved spectroscopy and a sample substitution method, we have measured the absorption and reduced scattering coefficients of blood-free perfused rat livers, isolated hepatocyte suspensions, and isolated mitochondria suspensions. A subsequent extrapolation of the isolated mitochondria data to the in vivo mitochondrial content and a comparison with the whole liver measurements lead to the following conclusions: 1) the mitochondria account for about 50% of the liver absorption coefficient at 780 nm (mu a = 0.25 cm-1 extrapolated from isolated mitochondria vs. 0.53 +/- 0.05 cm-1 measured for the liver); and 2) the mitochondrial compartment is the primary factor for the light scattering in the rat liver (mu s' = 15.5 cm-1 extrapolated from the isolated mitochondria versus 15.9 +/- 2.4 cm-1 measured for the liver), demonstrating the relevancy of our preliminary theoretical study.

References

    1. Methods Cell Biol. 1989;29:103-23
    1. Biochim Biophys Acta. 1989 Mar 23;973(3):355-82
    1. J Cell Biol. 1966 Aug;30(2):269-97
    1. J Cell Biol. 1968 Apr;37(1):27-46
    1. J Cell Biol. 1969 Jul;42(1):68-91
    1. J Biol Chem. 1969 Nov 25;244(22):6087-93
    1. J Cell Biol. 1972 Aug;54(2):325-45
    1. Science. 1973 Aug 24;181(4101):749-51
    1. J Cell Biol. 1977 Feb;72(2):441-55
    1. J Cell Biol. 1978 May;77(2):565-83
    1. Biophys J. 1988 Dec;54(6):1179-83
    1. J Cell Biol. 1978 Jun;77(3):887-901
    1. Proc Natl Acad Sci U S A. 1980 Feb;77(2):990-4
    1. Biochim Biophys Acta. 1981 Jan 14;634(1):1-10
    1. Biochem J. 1983 Aug 15;214(2):395-404
    1. J Cell Sci. 1984 Mar;66:21-38
    1. J Cell Biol. 1986 Jan;102(1):97-103
    1. Nature. 1987 Jan 1-7;325(6099):78-81
    1. Ann N Y Acad Sci. 1986;488:65-81
    1. Proc Natl Acad Sci U S A. 1988 Jul;85(14):4971-5
    1. Cytometry. 1988 Nov;9(6):636-41
    1. Anal Biochem. 1988 Nov 1;174(2):698-707
    1. Phys Med Biol. 1989 Dec;34(12):1901-16
    1. Biochim Biophys Acta. 1990 Jul 25;1018(2-3):190-3
    1. Biomed Biochim Acta. 1990;49(7):563-71
    1. Proc Natl Acad Sci U S A. 1991 May 1;88(9):3671-5
    1. Anal Biochem. 1991 Jan;192(1):149-55
    1. Anal Biochem. 1991 Jun;195(2):330-51
    1. J Gastroenterol Hepatol. 1992 Sep-Oct;7(5):486-90
    1. J Cell Physiol. 1993 Feb;154(2):248-53
    1. Anal Biochem. 1993 Sep;213(2):378-85
    1. Cell Biophys. 1993 Aug-Dec;23(1-3):1-2
    1. Biochim Biophys Acta. 1956 Feb;19(2):297-9

Source: PubMed

3
구독하다