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斑泥螈(两栖纲:有尾目)肝细胞的分离与原代培养

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

作者信息

Prelovsek Petra-Maja, Batista Urska, Bulog Boris

机构信息

Department of Biology, University of Ljubljana, Slovenia.

出版信息

In Vitro Cell Dev Biol Anim. 2006 Sep-Oct;42(8-9):255-62. doi: 10.1290/0601008.1.

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.

摘要

为了评估它们在生理学和生态毒理学研究中的适用性,采用两步胶原酶灌注法从黄斑泥螈(Necturus maculosus)中分离肝细胞。使用光学显微镜、电子显微镜和生化分析对原代培养的肝细胞进行了14天的研究。典型的灌注每克体重可产生1.7×10⁵个活肝细胞,平均活力为86±5%。大多数分离的细胞保持悬浮状态并形成聚集体。原代培养的肝细胞活力取决于胎牛血清(FCS)浓度和孵育温度。在补充有5% FCS的Leibovitz L - 15培养基中,8℃时活力最佳。新鲜分离的肝细胞的超微结构特征与黄斑泥螈体内肝细胞的特征相似。虽然肝细胞活力在培养14天内保持相对稳定(约80%),但电子显微镜分析显示在超微结构水平上有变化。大多数肝细胞在培养4天内保持与体内相似的结构特征。随着培养时间的增加,观察到细胞极性丧失、粗面内质网断裂、自噬体形成以及细胞糖原沉积物的相继耗尽。通过酪氨酸转氨酶诱导评估的功能完整性在培养期间下降。超微结构和生化分析表明需要进一步改善培养条件。然而,原代培养长达4天的分离肝细胞可推荐作为低等脊椎动物生理学和毒理学研究的模型。

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