Stem Cells Could Halt Osteoporosis, Promote Bone Growth - New Pathway That Controls Bone Remodelling

Main Category: Stem Cell Research
Also Included In: Bones / Orthopedics
Article Date: 10 Mar 2009 - 6:00 PDT

email icon email to a friend   printer icon printer friendly   write icon opinions  

Current Article Ratings:

Patient / Public:5 stars

4.75 (4 votes)

Healthcare Prof:not yet rated


While interferon gamma sounds like an outer space weapon, it's actually a hormone produced by our own bodies, and it holds great promise to repair bones affected by osteoporosis. In a new study published in the journal Stem Cells, researchers from the Aging Bone Research Program together with investigators at the Research Institute of the McGill University Health Centre (MUHC) explain that tweaking a certain group of multipotent stem cells (called mesenchymal stem cells) with interferon (IFN) gamma may promote bone growth. "We have identified a new pathway, centered on IFN gamma, that controls the bone remodelling process both in-vivo and in-vitro," explains A/Prof. Duque, the study's lead author and Director of the Aging Bone Research Centre at Nepean Clinical School. "More studies are required to describe it more precisely, but we are hopeful that it could lead to a better understanding of the underlying causes of osteoporosis, as well as to innovative treatments."

From cell culture to animal model - "First, we stimulated cultured mesenchymal stem cells to turn into bone cells (osteoblasts) in-vitro," says A/Prof. Duque, an Associate Professor with the University of Sydney Faculty of medicine. "We realised that this differentiation process involved IFN gamma-related genes, but also that these bone cells precursors could both be stimulated by IFN gamma and produced IFN gamma." The next step was to move to an animal model where IFN gamma effect is blocked by inactivating its receptor, a model called IFN gamma receptor knock-out. Bone density tests, comparable to those used to diagnose people with osteoporosis, were conducted. The results revealed that these animals have significantly lower bone mass than their healthy counterparts In addition, their mesenchymal stem cells have a decreased ability to make bone. "These findings confirm that IFN gamma is an integral factor for mesenchymal stem cells' differentiation into osteoblasts also in-vivo," says A/Prof. Duque.

New biological pathway, now hope for treatments - Both in-vitro and in-vivo results proved that IFN gamma is key to the differentiation of mesenchymal cells into bone cells, and to growth process of the bone. The exact pathway by which IFN acts on bone cells' formation will require more research to be described, but the strict correlation highlighted in this study leaves no doubt on its importance. Until now, IFN gamma has been mostly used as an agent to prevent infections and to reinforce the immune system from illnesses such as cancer. These findings provide hope that IFN gamma itself, or another molecule involved in its pathway, could soon also become an efficient drug-target for an antidote for osteoporosis.

About osteoporosis - Osteoporosis is a disease in which bones become fragile and more likely to break. If left untreated, osteoporosis can progress painlessly until a bone fractures in the hip, spine and wrist. According to the World Health Organization, osteoporosis affects one in four women over the age of 50.

Partners - "Autocrine Regulation of Interferon gamma in Mesenchymal Stem Cells Plays a Role in Early Osteoblastogenesis," published in the journal Stem Cells, was authored by A/Professor Duque from University of Sydney-Nepean Clinical School, and Richard Kremer, Dao Chao Huang, Michael Macoritto, Xian Fang Yang of the McGill University Faculty of Medicine and Centre for Bone and Periodontal Research and Daniel Rivas of the McGill-affiliated Lady Davis Institute for Medical Research.

Funding - This study was supported by the University of Sydney Medical Research Foundation, the Canadian Institutes for Health Research, the Dairy Farmers of Canada, the Natural Sciences and Engineering Research Council of Canada and the Fond de la Recherche en Santé du Québec.

About Stem Cells: The International Journal of Cell Differentiation and Proliferation: http://stemcells.alphamedpress.org

About the Aging Bone Research Centre
http://www.boneresearch.edu.au

Source
Gustavo Duque, MD, PhD
Associate Professor of Geriatric Medicine
Head Discipline of Geriatric Medicine
Director Aging Bone Research Program
Nepean Clinical School - University of Sydney
Level 5 South Block
Nepean Hospital
PO Box 63, Penrith, NSW
Australia 2750
http://www.agingbone.med.usyd.edu.au

Aging Bone Research Centre

Article adapted by Medical News Today from original press release.
Visit our stem cell research section for the latest news on this subject.
There are no references listed for this article.
Please use one of the following formats to cite this article in your essay, paper or report:

MLA
Aging Bone Research Centre. "Stem Cells Could Halt Osteoporosis, Promote Bone Growth - New Pathway That Controls Bone Remodelling." Medical News Today. MediLexicon, Intl., 10 Mar. 2009. Web.
14 Feb. 2012. <http://www.medicalnewstoday.com/releases/141725.php>

APA
Aging Bone Research Centre. (2009, March 10). "Stem Cells Could Halt Osteoporosis, Promote Bone Growth - New Pathway That Controls Bone Remodelling." Medical News Today. Retrieved from
http://www.medicalnewstoday.com/releases/141725.php.

Please note: If no author information is provided, the source is cited instead.


Stem Cell Research

What are Stem Cells?

Stem cells are a class of undifferentiated cells that are able to differentiate into specialized cell types. Commonly, stem cells come from two main sources: embryonic stem cells and adult stem cells Read more...

Most Popular Articles



Follow Our Stem Cell Research News On Twitter

Follow Us On Twitter
Get the latest news for this category delivered straight to your Twitter account. Simply visit our Stem Cell Research Twitter account and select the 'follow' option.



View list of all 'What Is...' articles »