You are hereFebruary 6, 2017
UW scientists find key cues to regulate bone-building cells
The prospect of regenerating bone lost to cancer or trauma is a step closer to the clinic as University of Wisconsin–Madison scientists have identified two proteins found in bone marrow as key regulators of the master cells responsible for making new bone.
In a study published online February 2 in Stem Cell Reports, a team of UW–Madison scientists reported that the proteins govern the activity of mesenchymal stem cells — precursor cells found in marrow that make bone and cartilage. The discovery opens the door to devising implants seeded with cells that can replace bone tissue lost to disease or injury.
"These are pretty interesting molecules," explained Wan-Ju Li, Ph.D., a UW–Madison professor of orthopedics and biomedical engineering, of the bone marrow proteins lipocalin-2 and prolactin. "We found that they are critical in regulating the fate of mesenchymal stem cells."
Dr. Li and Tsung-Lin Tsai, a UW–Madison postdoctoral researcher, scoured donated human bone marrow using high-throughput protein arrays to identify proteins of interest and then determined the activity of mesenchymal stem cells exposed to the proteins in culture. A goal of the study, Dr. Li said, is to better understand the bone marrow niche where mesenchymal stem cells reside in the body so that researchers can improve culture conditions for growing the cells in the lab and for therapy.
The researchers found that exposing mesenchymal stem cells to a combination of lipocalin-2 and prolactin in culture reduces and slows senescence, the natural process that robs cells of their power to divide and grow. Dr. Li said keeping the cells happy and primed outside the body, but reining in their power to grow and make bone tissue until after they are implanted in a patient, is key.
The ability to precisely manipulate mesenchymal stem cells in the laboratory dish and keep them poised to divide and form bone on cue helps pave the way for using cell-bearing three-dimensional matrices to reconstruct large swaths of bone lost to tumors or major trauma. Because bone has some natural healing properties, things like breaks and fractures can often mend themselves. But when large pieces of bone are lost, clinical intervention is required.
The team successfully tested human cells treated with lipocalin-2 and prolactin to regrow bone by implanting them in mice with a calvarial defect, where part of the skullcap had been surgically removed to model critical-sized bone loss.
The human marrow used in the new Wisconsin study was donated by patients undergoing hip replacement surgery. A caveat to the study, then, is that the protein factors identified came from donors with osteoarthritis. However, Dr. Li expressed confidence that the factors from the marrow used in the study would be similar or identical to what occurs in a healthy patient. The new study, he said, demonstrates a key improvement to the lab culture environment, which seeks to mimic the bone marrow niche where mesenchymal stem cells are found in the body.
Micrographs show the difference between treated and untreated bone cells in a mouse model of severe bone loss. Researchers have identified two native protein factors that help keep mesenchymal stem cells — the master cells that make bone and cartilage — happy in the laboratory dish. The work could one day help make regenerating lost bone in patients a reality. Image courtesy of Wan-Ju Li.