In vitro culture of functionally active buffalo hepatocytes isolated by using a simplified manual perfusion method

• Published in: PloS one 2015-03, Vol.10 (3), p.e0118841
• Main Authors: Panda, Santanu, Bisht, Sonu, Malakar, Dhruba, Mohanty, Ashok K, Kaushik, Jai K
• Format: Article
• Language: English
• Subjects: a1-antitrypsin; Agricultural economics; Albumin; Alpha 1-antitrypsin; Analysis; Animals; Antibodies; Azo Compounds; Biotechnology; Blotting, Western; Bromodeoxyuridine; Buffaloes; Cell culture; Cell Culture Techniques - methods; Cell Separation - methods; Collagen; Collagens; Cytochromes; Cytokeratin; Cytosol; DNA Primers - genetics; Drug metabolism; Drugs; Electrophoresis, Agar Gel; Enzymes; Farms; Gene expression; Gene regulation; Glucose; Glucose-6-phosphatase; Handbooks; Hepatocytes; Hepatocytes - cytology; Hepatocytes - physiology; In vitro methods and tests; In Vitro Techniques - methods; Keratin; Liver; Livestock; Lobes; Metabolism; Methods; Perfusion; Physical characteristics; Physiological aspects; Polarity; Protein-tyrosine-phosphatase; Proteins; Proteomics; Real-Time Polymerase Chain Reaction; Reverse Transcriptase Polymerase Chain Reaction; Rodents; Skin; Toxicity; Tyrosine; Viability
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0118841

In farm animals, there is no suitable cell line available to understand liver-specific functions. This has limited our understanding of liver function and metabolism in farm animals. Culturing and maintenance of functionally active hepatocytes is difficult, since they survive no more than few days. Establishing primary culture of hepatocytes can help in studying cellular metabolism, drug toxicity, hepatocyte specific gene function and regulation. Here we provide a simple in vitro method for isolation and short-term culture of functionally active buffalo hepatocytes. Buffalo hepatocytes were isolated from caudate lobes by using manual enzymatic perfusion and mechanical disruption of liver tissue. Hepatocyte yield was (5.3 ± 0.66)×107 cells per gram of liver tissue with a viability of 82.3 ± 3.5%. Freshly isolated hepatocytes were spherical with well contrasted border. After 24 hours of seeding onto fibroblast feeder layer and different extracellular matrices like dry collagen, matrigel and sandwich collagen coated plates, hepatocytes formed confluent monolayer with frequent clusters. Cultured hepatocytes exhibited typical cuboidal and polygonal shape with restored cellular polarity. Cells expressed hepatocyte-specific marker genes or proteins like albumin, hepatocyte nuclear factor 4α, glucose-6-phosphatase, tyrosine aminotransferase, cytochromes, cytokeratin and α1-antitrypsin. Hepatocytes could be immunostained with anti-cytokeratins, anti-albumin and anti α1-antitrypsin antibodies. Abundant lipid droplets were detected in the cytosol of hepatocytes using oil red stain. In vitro cultured hepatocytes could be grown for five days and maintained for up to nine days on buffalo skin fibroblast feeder layer. Cultured hepatocytes were viable for functional studies. We developed a convenient and cost effective technique for hepatocytes isolation for short-term culture that exhibited morphological and functional characteristics of active hepatocytes for studying gene expression, regulation, hepatic genomics and proteomics in farm animals.