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Cross-section of the human liver.
- Protein synthesis
- Protein storage
- Transformation of carbohydrates
- Synthesis of cholesterol, bile salts and phospholipids
- Detoxification, modification, and excretion of exogenous and endogenous substances
- Initiation of formation and secretion of bile
Smooth endoplasmic reticulum is abundant in hepatocytes, whereas most cells in the body have only small amounts.
Hepatocytes display an eosinophilic cytoplasm, reflecting numerous mitochondria, and basophilic stippling due to large amounts of rough endoplasmic reticulum and free ribosomes. Brown lipofuscin granules are also observed (with increasing age) together with irregular unstained areas of cytoplasm; these correspond to cytoplasmic glycogen and lipid stores removed during histological preparation. The average life span of the hepatocyte is 5 months; they are able to regenerate.
Hepatocyte nuclei are round with dispersed chromatin and prominent nucleoli. Anisokaryosis (or variation in the size of the nuclei) is common and often reflects tetraploidy and other degrees of polyploidy, a normal feature of 30-40% of hepatocytes in the adult human liver. Binucleate cells are also common.
Hepatocytes are organised into plates separated by vascular channels (sinusoids), an arrangement supported by a reticulin (collagen type III) network. The hepatocyte plates are one cell thick in mammals and two cells thick in the chicken. Sinusoids display a discontinuous, fenestrated endothelial cell lining. The endothelial cells have no basement membrane and are separated from the hepatocytes by the space of Disse, which drains lymph into the portal tract lymphatics.
Kupffer cells are scattered between endothelial cells; they are part of the reticuloendothelial system and phagocytose spent erythrocytes. Stellate (Ito) cells store vitamin A and produce extracellular matrix and collagen; they are also distributed amongst endothelial cells but are difficult to visualise by light microscopy.
The liver forms fatty acids from carbohydrates and synthesizes triglycerides from fatty acids and glycerol. Hepatocytes also synthesize apoproteins with which they then assemble and export lipoproteins (VLDL, HDL).
The liver receives many lipids from the systemic circulation and metabolizes chylomicron remnants. It also synthesizes cholesterol from acetate and further synthesizes bile salts. The liver is the sole site of bile salts formation.
One of the detoxifying functions of hepatocytes is to modify ammonia into urea for excretion.
The most abundant organelle in liver cell is the smooth endoplasmic reticulum.
Hepatocyte isolation and culture
Primary hepatocytes are commonly used in cell biological and biopharmaceutical research. In vitro model systems based on hepatocytes have been of great help to better understand the role of hepatocytes in (patho)physiological processes of the liver. In addition, pharmaceutical industry has heavily relied on the use of hepatocytes in suspension or culture to explore mechanisms of drug metabolism and even predict in vivo drug metabolism. For these purposes, hepatocytes are usually isolated from animal or human whole liver or liver tissue by collagenase digestion, which is a two-step process. In the first step, the liver is placed in an isotonic solution, in which calcium is removed to disrupt cell-cell tight junctions by the use of a calcium chelating agent. Next, a solution containing collagenase is added to separate the hepatocytes from the liver stroma. This process creates a suspension of hepatocytes, which can be seeded in multi-well plates and cultured for many days or even weeks. For optimal results, culture plates should first be coated with an extracellular matrix (e.g. collagen, Matrigel) to promote hepatocyte attachment (typically within 1-3 hr after seeding) and maintenance of the hepatic phenotype. In addition, and overlay with an additional layer of extracellular matrix is often performed to establish a sandwich culture of hepatocytes. The application of a sandwich configuration supports prolonged maintenance of hepatocytes in culture. Freshly-isolated hepatocytes that are not used immediately can be cryopreserved and stored. They do not proliferate in culture. Hepatocytes are intensely sensitive to damage during the cycles of cryopreservation including freezing and thawing. Even after the addition of classical cryoprotectants there is still damage done while being cryopreserved. Nevertheless, recent cryopreservation and resuscitation protocols support application of cryopreserved hepatocytes for most biopharmaceutical applications.
- Ley, Brian (1999). "Diameter of a Human Hair". Archived from the original on 2010-06-28. Retrieved 2010-06-28.
- Lodish, H., Berk, A., Zipursky, S. L., Matsudaira, P., Baltimore, D., Darnell, J. E. Molecular Cell Biology (Fifth Edition). W. H. Freeman and Company. New York, 2000, pp 10.
- Celton-Morizur, S; Merlen, G; Couton, D; Desdouets, C (1 February 2010). "Polyploidy and liver proliferation: central role of insulin signaling." (PDF). Cell cycle (Georgetown, Tex.). 9 (3): 460–6. PMID 20090410. doi:10.4161/cc.9.3.10542. Archived from the original (PDF) on 2012-04-25.
- Ali ES, Hua J, Wilson CH, Tallis GA, Zhou FH, Rychkov GY, Barritt GJ (2016). "The glucagon-like peptide-1 analogue exendin-4 reverses impaired intracellular Ca2+ signalling in steatotic hepatocytes". BBA-Molecular Cell Research. 1863: 2135–46. PMID 27178543. doi:10.1016/j.bbamcr.2016.05.006.
- Lecluyse EL, Alexandre E (2010). "Isolation and culture of primary hepatocytes from resected human liver tissue". Methods Mol Biol. 640: 57–82. PMID 20645046. doi:10.1007/978-1-60761-688-7_3.
- Dunn JC, Yarmush ML, Koebe HG, Tompkins RG (Feb 1989). "Hepatocyte function and extracellular matrix geometry: long-term culture in a sandwich configuration". FASEB J. 3 (2): 174–7. Erratum in: FASEB J 1989 May;3(7):1873. PMID 2914628.
- De Bruyn T, Chatterjee S, Fattah S, Keemink J, Nicolaï J, Augustijns P, Annaert P (May 2013). "Sandwich-cultured hepatocytes: utility for in vitro exploration of hepatobiliary drug disposition and drug-induced hepatotoxicity". Expert Opin Drug Metab Toxicol. 9 (5): 589–616. PMID 23452081. doi:10.1517/17425255.2013.773973.
- Li Albert P (2001). "Screening for human ADME/Tox drug properties in Drug Discovery". Drug Discovery Today. 6 (7): 357–366. doi:10.1016/s1359-6446(01)01712-3.
- Hamel, F.; Grondin, M. L.; Denizeau, F.; Averill-Bates, D. A.; Sarhan, F. (2006). "Wheat extracts as an efficient cryoprotective agent for primary cultures of rat hepatocytes". Biotechnology and Bioengineering. 95 (4): 661–670. PMID 16927246. doi:10.1002/bit.20953.
- De Bruyn T, Ye ZW, Peeters A, Sahi J, Baes M, Augustijns PF, Annaert PP (Jul 2011). "Determination of OATP-, NTCP- and OCT-mediated substrate uptake activities in individual and pooled batches of cryopreserved human hepatocytes". Eur J Pharm Sci. 43 (4): 297–307. PMID 21605667. doi:10.1016/j.ejps.2011.05.002.
- Histology image: 22101ooa – Histology Learning System at Boston University - "Ultrastructure of the Cell: hepatocytes and sinusoids"
- Hepatic Histology: Hepatocytes (Colorado State University
- The use of hepatocytes to measure clearance The performance of in vitro hepatic clearance studies including analysis of the data.