Andrea Page-McCaw, Ph.D.
Professor of Cell and Developmental Biology
Director of Graduate Studies (DGS)
AAAS Fellow - 2018
- : firstname.lastname@example.org
- : (615) 875-5841
U 4213 A Medical Research Building 3
465 21st Avenue South
Nashville, - 37232-8240
4206 Medical Research Building 3
Matrix metalloproteinases (MMPs), tissue remodeling, wound healing, developmental biology, Drosophila, genetics, receptor, and signaling, immunity.
During embryogenesis, animals develop complex structures, but they often have to modify their morphology to meet the demands of continuing growth or environmental challenge. This is known as tissue remodeling. Tissue remodeling is also required for animals to heal wounds, and it goes awry during cancer when tumors usurp tissue remodeling functions to promote metastasis. The matrix metalloproteinase (MMP) family of extracellular proteases is required for tissue remodeling events throughout the animal kingdom. These proteases are also upregulated in cancer and many inflammatory conditions such as arthritis. Understanding how MMPs promote tissue remodeling, both in normal and pathological circumstances, is a central question in my laboratory.
Drosophila melanogaster (the common fruitfly) has been an important model organism for understanding cell and developmental biology because of their advanced genetics and beautiful cytology. Although mammals have about 24 MMPs with overlapping substrate specificity and functional redundancy, Drosophila has only two MMPs, greatly simplifying genetic analysis of MMP function. We have found MMPs to be absolutley required for developmental tissue remodeling and epidermal wound healing in our system. We are currently investigating how basement membrane is modified and expanded in coordination with tissue growth during development.