Literature DB >> 15805053

New insights into functional aspects of liver morphology.

David E Malarkey1, Kennita Johnson, Linda Ryan, Gary Boorman, Robert R Maronpot.   

Abstract

The liver is structurally and functionally complex and has been considered second only to brain in its complexity. Many mysteries still exist in this heterogeneous tissue whose functional unit of the lobule has continued to stump morphologists for over 300 years. The primary lobule, proposed by Matsumoto in 1979, has been gaining acceptance as the functional unit of the liver over other conceptual views because it's based on vessel architecture and includes the classic lobule as a secondary feature. Although hepatocytes comprise almost 80% of the liver, there are at least another dozen cell types, many of which provide "cross-talk" and play important functional roles in the normal and diseased liver. The distribution and functional roles of all cells in the liver must be carefully considered in both the analysis and interpretation of research data, particularly data in the area of genomics and "phenotypic anchoring" of gene expression results. Discoveries regarding the functional heterogeneity of the various liver cell types, including hepatocytes, hepatic stellate cells, sinusoidal endothelia, and Kupffer cells, are providing new insights into our understanding of the development, prevention and treatment of liver disease. For example, functional differences along zonal patterns (centrilobular or periportal) have been demonstrated for sinusoidal endothelium, Kupffer cells, and hepatocytes and can explain the gradients and manifestations of disease observed within lobules. Intralobular gradients of bile uptake, glycogen depletion, glutamine synthetase, and carboxylesterase by hepatocytes; widened fenestrations in centrilobular sinusoidal lining cells; and differences in the components of centrilobular extracellular matrix or function of Kupffer cells have been demonstrated. Awareness of the complexities and heterogeneity of the liver will add to a greater understanding of liver function and disease processes that lead to toxicity, cancer, and other diseases.

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Year:  2005        PMID: 15805053     DOI: 10.1080/01926230590881826

Source DB:  PubMed          Journal:  Toxicol Pathol        ISSN: 0192-6233            Impact factor:   1.902


  59 in total

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Review 2.  Molecular mechanisms underlying chemical liver injury.

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3.  Diagnostic and therapeutic potentials of microRNAs in cholangiopathies.

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4.  Hepatic tight junctions: from viral entry to cancer metastasis.

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Review 5.  Understanding the marvels behind liver regeneration.

Authors:  Anan Abu Rmilah; Wei Zhou; Erek Nelson; Li Lin; Bruce Amiot; Scott L Nyberg
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2019-03-28       Impact factor: 5.814

6.  Targeted inactivation of copper transporter Atp7b in hepatocytes causes liver steatosis and obesity in mice.

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Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2017-04-20       Impact factor: 4.052

7.  Biodistribution of small interfering RNA at the organ and cellular levels after lipid nanoparticle-mediated delivery.

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8.  Tissue engineering toward organ-specific regeneration and disease modeling.

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Journal:  MRS Commun       Date:  2017-07-31       Impact factor: 2.566

9.  Semecarpus anacardium (Bhallataka) Alters the Glucose Metabolism and Energy Production in Diabetic Rats.

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10.  Tissue compartment analysis for biomarker discovery by gene expression profiling.

Authors:  Antoine Disset; Lydie Cheval; Olga Soutourina; Jean-Paul Duong Van Huyen; Guorong Li; Christian Genin; Jacques Tostain; Alexandre Loupy; Alain Doucet; Rabary Rajerison
Journal:  PLoS One       Date:  2009-11-10       Impact factor: 3.240

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