Science News

... from universities, journals, and other research organizations

Crucial Hormonal Pathway To Bone Building Uncovered

ScienceDaily (Oct. 31, 2008) — Scientists have discovered a crucial step in hormone-triggered bone growth, a finding that could lead to new osteoporosis drugs and better bone-building therapies, according to a new study.

The research was performed at the University of Alabama at Birmingham (UAB). It showed that parathyroid hormone (PTH) given intermittently enhances the body's own bone-building action through a specific "co-receptor" on the surface of bone cells.

Previously, PTH was known to stimulate bone formation, but the exact mechanism was unknown, the UAB researchers said. The findings are published in the journal Genes and Development.

"Our study uncovers a novel mechanism for how parathyroid hormone signaling selectively stimulates bone formation," said Xu Cao, Ph.D., UAB professor of pathology and senior author on the study. "We have identified the protein co-receptor crucial to the whole process."

The UAB researchers focused on PTH signals in mice, testing to see which cell receptors actively recruited calcium from the blood. They uncovered the one co-receptor responsible for turning on bone building, said Mei Wan, Ph.D., UAB associate professor of molecular and cellular pathology and first author on the study.

Previously, the exact mechanism of PTH-signaled bone formation was shrouded by the joint production of osteoblasts and osteoclasts, said Jay McDonald, M.D., pathology professor and director of UAB's Center for Metabolic Bone Disease. Both types of cells are instrumental in regulating a healthy skeleton – osteoblasts by forming new bone, and osteoclasts by resorbing old and brittle bone.

Many osteoporosis drugs now target both osteoblasts and osteoclasts, which can lead to zero or minimal bone formation, McDonald said.

"The ideal would be to have one drug to shut down the osteoclasts and turn on the osteoblasts to effectively build bone. We don't have that yet, but this study shows us the path to get there," he said.

FORTEO® is the only approved PTH drug for use in postmenopausal women with osteoporosis, and in men with hormone-linked osteoporosis. Many experts hope the approved drug is part of the next wave of medicines that work to build back bone, reduce bone loss and minimize fracture risks in the aging.

The study was a partnership between UAB and researchers at Children's Hospital Boston, Harvard Medical School in Boston and Shihezi Medical College in Xinjiang, China. Funding came from the U.S. National Institutes of Health.

Recommend this story on Facebook, Twitter,
and Google +1:

Other bookmarking and sharing tools:

| More

Story Source:

The above story is reprinted from materials provided by University of Alabama at Birmingham.

Note: Materials may be edited for content and length. For further information, please contact the source cited above.


APA

MLA

Note: If no author is given, the source is cited instead.

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of ScienceDaily or its staff.

Search ScienceDaily

Number of stories in archives: 114,900

Find with keyword(s):
 
Enter a keyword or phrase to search ScienceDaily's archives for related news topics,
the latest news stories, reference articles, science videos, images, and books.

 
  more breaking science news

Social Networks


Recommend this story on Facebook, Twitter,
and Google +1:
Other bookmarking and sharing tools:
| More

Breaking News

... from NewsDaily.com

In Other News ...

Copyright Reuters 2008. See Restrictions.

Free Subscriptions

... from ScienceDaily

Get the latest science news with our free email newsletters, updated daily and weekly. Or view hourly updated newsfeeds in your RSS reader:

Feedback

... we want to hear from you!

Tell us what you think of ScienceDaily -- we welcome both positive and negative comments. Have any problems using the site? Questions?

 
Post this page to your favorite social bookmarking site:
close
Include this item in your blog or web site:
close
Cite this article in your essay, paper, or report:
close
Email this page's link to a friend or colleague:
close