The discovery may pave the way for potential new strategies to treat the blood disorders and further illuminates the relationship between inflammation and cancer, said lead investigator Nadia Carlesso, associate professor of pediatrics at the Indiana University School of Medicine.
Bone marrow includes the cells that produce the body's red and white blood system cells in a process called hematopoiesis. The marrow also provides a support system and "home" for the blood-producing cells called the hematopoietic microenvironment.
The new research demonstrates the importance of the hematopoietic microenvironment in the development of a group of potentially deadly diseases called myeloproliferative disorders.
"It has been known for years that there are links between inflammation and cancer, but these studies have been challenged by the lack of genetic models, especially for blood-based malignancies," said Carlesso.
The researchers focused on what happens when there are abnormally low levels of a molecule called Notch, which plays an important role in the process of blood cell production.
Using a genetically modified mouse, they found that the loss of Notch function in the microenvironment causes a chain of molecular events that result in excess production of inflammatory factors.
The high levels of inflammation in the bone marrow were associated with the development of a myeloproliferative disorder in the mice.
Myeloproliferative diseases in humans can result in several illnesses caused by overproduction of myeloid cells, which are normally are used to fight infections.
These diseases can put patients at risk for heart attack or stroke, and frequently progress into acute leukemia and bone marrow failure, which have fatal outcomes.
When Carlesso's team blocked the activity of one of the molecules in this biochemical cascade, the myeloproliferative
disorder in the mice was reversed.
In addition, elevated levels of the blocked molecule were found in samples from human patients with myeloproliferative disease.
These findings suggest that developing drugs that target this inflammatory reaction at different key points could be a promising strategy to limit the development of myeloproliferative disease in humans.
The molecular cascade leading to inflammation was not occurring directly in the bone marrow cells that produce blood
cells, but in cells of the bone marrow microenvironment, especially in endothelial cells that line the capillaries - tiny blood vessels - inside the bone marrow. This was a key discovery, Carlesso said.