Biol Reprod Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


BOR - Papers in Press, published online ahead of print May 9, 2007.
Biol Reprod 2007, 10.1095/biolreprod.106.055244
This Article
Right arrow Full Text (Rapid PDF)
Right arrow All Versions of this Article:
77/3/577    most recent
biolreprod.106.055244v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ilancheran, S.
Right arrow Articles by Manuelpillai, U.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ilancheran, S.
Right arrow Articles by Manuelpillai, U.
Agricola
Right arrow Articles by Ilancheran, S.
Right arrow Articles by Manuelpillai, U.
Submitted July 2, 2006
Returned for revision August 21, 2006
Accepted April 30, 2007

Pregnancy


Stem Cells Derived from Human Fetal Membranes Display Multi-Lineage Differentiation Potential

Sivakami Ilancheran , Anna Michalska , Gary Peh , Euan M Wallace , Martin Pera , and Ursula Manuelpillai *

* To whom correspondence should be addressed. E-mail: ursula.manuelpillai{at}med.monash.edu.au.

Abstract
The amnion is the inner of two membranes surrounding the fetus. That it arises from embryonic epiblast cells prior to gastrulation suggests that it may retain a reservoir of stem cells throughout pregnancy. We found that human amniotic epithelial cells (hAECs) harvested from term delivered fetal membranes express mRNA and proteins present in human embryonic stem cells (hESCs), including POU domain, class 5, transcription factor 1, Nanog homeobox, SRY-box 2 and stage-specific embryonic antigen-4. In keeping with possible stem cell-like activity, hAECs were also clonogenic and primary hAEC cultures could be induced to differentiate into cardiomyocytic, myocytic, osteocytic, adipocytic (mesodermal), pancreatic, hepatic (endodermal), neural and astrocytic (neuro-ectodermal) cells in vitro, as defined by phenotypic, mRNA expression, immunocytochemical and/or ultrastructural characteristics. However, unlike hESCs, hAECs did not form teratomas upon transplantation into SCID mice testes. Lastly, using flow cytometry we have shown that only a very small proportion of primary hAECs contain Class IA and Class II Human Leukocyte Antigens (HLA), consistent with a low risk of tissue rejection. However, following differentiation into hepatic and pancreatic lineages significant proportions of cells contained Class IA, but not Class II, HLA. These observations suggest that the term amnion, an abundant and easily accessible tissue, may be a useful source of multipotent stem cells that possess a degree of immune privilege.

Key words: Developmental biology • Placenta • fetal membranes • amnion • stem cells


This article has been cited by other articles:


Home page
Stem CellsHome page
O. Parolini, F. Alviano, G. P. Bagnara, G. Bilic, H.-J. Buhring, M. Evangelista, S. Hennerbichler, B. Liu, M. Magatti, N. Mao, et al.
Concise Review: Isolation and Characterization of Cells from Human Term Placenta: Outcome of the First International Workshop on Placenta Derived Stem Cells
Stem Cells, February 1, 2008; 26(2): 300 - 311.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Copyright © 2007 by the Society for the Study of Reproduction.