A new study revealed that mechanical forces affect the growth and remodeling of blood vessels during tissue regeneration and wound healing. The forces diminish or enhance the vascularization process and tissue regeneration depending on when they are applied during the healing process.
The study found that applying mechanical forces to an injury site immediately after healing began disrupted vascular growth into the site and prevented bone healing. However, applying mechanical forces later in the healing process enhanced functional bone regeneration. The study’s findings could influence treatment of tissue injuries and recommendations for rehabilitation.
“Our finding that mechanical stresses caused by movement can disrupt the initial formation and growth of new blood vessels supports the advice doctors have been giving their patients for years to limit activity early in the healing process,” Robert Guldberg, professor in the George W. Woodruff School of Mechanical Engineering at the Georgia Institute of Technology, stated in a press release. “However, our findings also suggest applying mechanical stresses to the wound later on can significantly improve healing through a process called adaptive remodeling.”
The study was published in the journal, Proceedings of the National Academy of Sciences. The research was supported by the National Institutes of Health, the Armed Forces Institute of Regenerative Medicine and the U.S. Department of Defense.
Because blood vessel growth is required for the regeneration of many different tissues, including bone, Guldberg and former Georgia Tech graduate student Joel Boerckel used healing of a bone defect in rats for their study. Following removal of eight millimeters of femur bone, they treated the gap with a polymer scaffold seeded with a growth factor called recombinant human bone morphogenetic protein-2 (rhBMP-2), a potent inducer of bone regeneration. The scaffold was designed in collaboration with Nathaniel Huebsch and David Mooney from Harvard University.
The experiments showed that exerting mechanical forces on the injury site immediately after healing began significantly inhibited vascular growth into the bone defect region. The volume of blood vessels and their connectivity were reduced by 66% and 91% respectively, compared with the group for which no force was applied. The lack of vascular growth into the defect produced a 75% reduction in bone formation and failure to heal the defect.
But the study found that the same mechanical force that hindered repair early in the healing process became helpful later on.
When the injury site experienced no mechanical force until 4 weeks after the injury, blood vessels grew into the defect and vascular remodeling began. With delayed loading, the researchers observed a reduction in quantity and connectivity of blood vessels, but the average vessel thickness increased. In addition, bone formation improved by 20% compared with when no force was applied, and strong tissue biomaterial integration was evident.
“We found that having a very stable environment initially is very important because mechanical stresses applied early on disrupted very small vessels that were forming,” Guldberg, who is also the director of the Petit Institute for Bioengineering and Bioscience at Georgia Tech said. “If you wait until those vessels have grown in and they’re a little more mature, applying a mechanical stimulus then induces remodeling so that you end up with a more robust vascular network.”
The study’s results may help researchers optimize the mechanical properties of tissue regeneration scaffolds in the future.
“Our study shows that one might want to implant a material that is stiff at the very beginning to stabilize the injury site but becomes more compliant with time, to improve vascularization and tissue regeneration,” Guldberg added.