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. 2006 Sep-Oct;42(8-9):255-62.
doi: 10.1290/0601008.1.

Isolation and primary culture of Necturus maculosus (Amphibia: Urodela) hepatocytes

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Isolation and primary culture of Necturus maculosus (Amphibia: Urodela) hepatocytes

Petra-Maja Prelovsek et al. In Vitro Cell Dev Biol Anim. 2006 Sep-Oct.

Abstract

In order to evaluate their suitability for physiological and ecotoxicological studies, hepatocytes were isolated from the common mudpuppy (Necturus maculosus) using a two-step collagenase perfusion. Hepatocytes in primary culture were investigated for 14 d using light and electron microscopy and biochemical analyses. A typical perfusion yielded 1.7 x 10(5) viable hepatocytes per gram body weight with an average viability of 86 +/- 5%. The majority of isolated cells remained in suspension and formed aggregates. The viability of hepatocytes in primary culture was dependent on a fetal calf serum (FCS) concentration and incubation temperature. Viability was best at 8 degrees C in Leibovitz L-15 medium supplemented with 5% FCS. The ultrastructural characteristics of freshly isolated hepatocytes resembled those of N. maculosus hepatocytes in vivo. Whereas hepatocyte viability remained relatively stable (around 80%) up to 14 d in culture, electron microscopic analyses revealed changes at ultrastructural level. The majority of hepatocytes retained similar structural characteristics to those in vivo up to 4 d. Loss of cellular polarity, fractionation of rough endoplasmic reticulum, formation of autophagosomes, and successive exhaustion of cellular glycogen deposits were observed with increased time in culture. Functional integrity, as estimated by tyrosine aminotransferase induction, decreased during the culture period. Ultrastructural and biochemical analyses indicate the need for further improvement of culture conditions. Nevertheless, isolated hepatocytes in primary culture for up to 4 d can be recommended as a model for physiological and toxicological studies in lower vertebrates.

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References

    1. FEBS Lett. 1987 Nov 2;223(2):223-6 - PubMed
    1. Exp Cell Res. 1981 Feb;131(2):363-71 - PubMed
    1. J Cell Physiol. 1998 Apr;175(1):41-9 - PubMed
    1. In Vitro Cell Dev Biol. 1985 Apr;21(4):221-8 - PubMed
    1. Arch Biochem. 1950 Jan;25(1):191-200 - PubMed

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