The many ways to mend your liver: A critical appraisal. Issue 3 (7th June 2018)

• Record Type: Journal Article
• Authors: Alison, Malcolm R.
• Is Part Of: International journal of experimental pathology. Volume 99:Issue 3(2018:Jun.)
• Page Start: 106
• Page End: 112
• Publication Date: 2018-06-07
• Subjects: axis inhibition protein 2 -- hepatic progenitor cells -- hybrid hepatocytes -- leucine‐rich‐repeat‐containing G protein‐coupled receptor 5 -- Mdm2 -- R‐spondin‐1 -- Sry [sex determining region Y] box 9 -- telomerase reverse transcriptase; Pathology, Experimental -- Periodicals; 616.07
• DOI: 10.1111/iep.12272
• Languages: English
• ISSNs: 0959-9673

Abstract

Summary: In the latter half of the 20th century, our understanding of mammalian liver regeneration was shaped by the manner of compensatory hyperplasia occurring after a partial rat liver resection. This response involves almost all hepatocytes and thus is unlikely to be the outcome of the multiple cycling of a small stem cell population. It was most intense in the outer third of lobule, the location closest to the afferent arterial blood supply. With the advent of heritable genetic labelling techniques, usually applied to mice, hitherto unrecognized hepatocytes with clonogenic potential have been discovered, contributing to homoeostatic renewal and/or regenerative responses after tissue loss. This review combines observations from cell lineage tracing studies with other data to summarize the Four proposed anatomical locations for hepatocyte stem cells: the periportal zone, the pericentral zone, a randomized distribution and finally within the intrahepatic biliary tree. As in other endodermal‐derived tissues, it appears that there are both homoeostatic stem cells and regenerative stem cells, while some normally homoeostatic stem cells can become more active to boost regeneration.