首页> 外文期刊>In Vitro Cellular and Developmental Biology. Animal: Journal of the Tissues Culture Association >Isolation and primary culture of Necturus maculosus (Amphibia: Urodela) hepatocytes
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Isolation and primary culture of Necturus maculosus (Amphibia: Urodela) hepatocytes

机译:猕猴肝(两栖动物:Urodela)肝细胞的分离和原代培养

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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.
机译:为了评估其在生理学和生态毒理学研究中的适用性,使用两步胶原酶灌注法从普通的泥mud(Necturus maculosus)中分离出肝细胞。使用光学和电子显微镜及生化分析研究原代培养的肝细胞14 d。典型的灌注产生每克体重1.7 x 10(5)个活肝细胞,平均生存力为86 +/- 5%。大多数分离的细胞保留在悬浮液中并形成聚集体。肝细胞在原代培养中的生存能力取决于胎牛血清(FCS)浓度和孵育温度。在添加5%FCS的Leibovitz L-15培养基中,活力在8摄氏度时最佳。新鲜分离的肝细胞在体内的超微结构特征类似于黄斑痣肝细胞的超微结构特征。肝细胞活力在培养至14 d时仍保持相对稳定(约80%),而电子显微镜分析显示超微结构水平发生了变化。大多数肝细胞保留了与体内相似的结构特征,直至4 d。随着培养时间的增加,观察到细胞极性的丧失,粗面内质网的分离,自噬体的形成以及细胞糖原沉积物的连续消耗。通过酪氨酸氨基转移酶诱导估计的功能完整性在培养期间降低。超微结构和生化分析表明需要进一步改善培养条件。然而,可以推荐将原代培养长达4 d的分离的肝细胞作为低等脊椎动物生理和毒理学研究的模型。

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