Identification and propagation of liver stem cells

Authors: Suzuki A.1; Nakauchi H.2, 3, 4

Source: Seminars in Cell and Developmental Biology, Volume 13, Number 6, December 2002 , pp. 455-461(7)

Publisher: Academic Press

Buy & download fulltext article:

OR

Price: $52.63 plus tax (Refund Policy)

Abstract:

Although the liver has been known for its enormous regenerative capacity, little is known about the mechanisms responsible for such regeneration.

To provide evidence for the existence of liver stem cell, using FACS and single cell-based assays, cells with multi-lineage differentiation potential and self-renewal capability have been prospectively identified. These cells could be clonally propagated in culture where they continuously produced hepatocytes and cholangiocytes as descendants while maintaining primitive stem cells. When the cells clonally expanded in vitro were transplanted into mouse, they morphologically and functionally differentiated into hepatocytes and cholangiocytes. Furthermore, these cells differentiated into pancreatic acinar cells or intestinal epithelial cells upon transplantation into pancreas or duodenal wall. Manipulation of self-renewing liver stem cells may provide new insight into therapies for diseases of the digestive system.

© 2002 Elsevier Science Ltd

Language: English

Document Type: Research article

DOI: http://dx.doi.org/10.1016/S1084-9521(02)00134-9

Affiliations: 1: Department of Surgery, Institute of Clinical Medicine, University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan 2: Department of Immunology, Institute of Basic Medical Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan 3: CREST (Japan Science and Technology Corporation), Tsukuba, Ibaraki 305-8575, Japan 4: Laboratory of Stem Cell Therapy, Center for Experimental Medicine, Institute of Medical Science, University of Tokyo, Tokyo 108-8639, Japan

Publication date: 2002-12-01

Related content

Tools

Key

Free Content
Free content
New Content
New content
Open Access Content
Open access content
Subscribed Content
Subscribed content
Free Trial Content
Free trial content

Text size:

A | A | A | A
Share this item with others: These icons link to social bookmarking sites where readers can share and discover new web pages. print icon Print this page