Researchers have mapped a cell mechanism that plays a key role in age-related bone loss. us suggest that the results not only shed light Above the biology of osteoporosis but should Apparently help to develop new drugs to treat the disease.

In the journal PNAS, scientists from both the University of Alabama at Birmingham And Zhejiang University in China explain how a protein called Cbf-beta is Important for controlling the rate at which new bone cells replace old ones.

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Osteoporosis is a disease in which bones become weak & brittle, increasing the risk of fractures. Bone is a living tissue that is constantly regenerating, & the body full maintains a balance – called homeostasis – between the creation of new bone cells and the removal of old cells.

As we age, the rate at which new bone replaces old or damaged bone slows down and bone density gradually diminishes. But if this rate slows too much, it can lead to osteoporosis.

Osteoporosis is a big global health problem & is more common in women than in men. Estimates suggest that around 1 in 3 women & 1 in 5 men over the age of 50 experience bone fractures due to osteoporosis.

In women over the age of 45, the disease accounts for more days spent in hospital than diabetes, heart attack,   http://radiologyebook.net/video-medical   And breast cancer.

In the United States, low bone mass and osteoporosis are thought to affect over 1/2 (55 percent) of people aged 50 And older.

Progenitor cells

Progenitor cells are immature cells that stand in reserve until They receive genetic instructions from transcription factors that tell them which type of cell to become. In the case of bone tissue, the progenitor cells are bone marrow "mesenchymal stem cells."

Depending Above the instructions us receive, the mesenchymal stem cells can mature into: bone-producing cells called osteoblasts; cartilage-producing cells, or chondrocytes; And adipocytes, or obesity cells.

Until now, it was not clear what was controlling the direction of maturity of the progenitor cells so as to maintain the delicate flat or homeostasis of bone formation.

When us investigated the transcription factors controlling the direction of maturity, the team found that a protein called core-binding factor subunit beta (Cbf-beta) was vital for switching destinations between bone-producing cell and Fat more cell.

To undertake the study, the team engineered three groups of mice by deleting Cbf-beta at three different stages in the maturation of the progenitor cells.

Cbf-beta plays key role

The team found that all three groups of mice developed severe osteoporosis and accumulated fats cells in their bone marrow. The pattern was similar to that seen in age-related bone loss.

us Apparently found increased Expression of Fat more cell genes in the progenitor cells – that is, the bone marrow mesenchymal stem cells – & bone cells of the skulls of mice lacking Cbf-beta.

Further investigation showed that when Cbf-beta activates a signal inside a type of cell known as Wnt10b/beta-catenin, it blocks Expression of the gene that directs the progenitor cells to mature into fat cells. In other words, it inhibits the "adipogenesis regulatory gene."

The team Apparently found that Cbf-beta drives progenitor cells to become bone-producing cells through another type of Wnt signal sent to nearby cells: the "Wnt paracrine pathway."

The researchers hope that their mapping will enhance understanding of the role that Cbf-beta plays in maintaining bone, especially as You age.

Source: General online