Matrix Metalloproteinase (MMPs) constitute a family of proteases primarily known for their matrix remodeling activity in several cancers and chronic inflammatory diseases. However, MMPs are also found in intracellular compartments including the nucleus of several cell types. MMP28 is the last identified member of the family, it is involved in wound repair, central nervous system development, and immune system maturation. In addition, MMP28 mis-regulation has been linked to several cancers. MMP28 activity can induce epithelial-to- mesenchymal transition (EMT) and migration in human alveolar epithelium where it has been described in the cell nucleus. Very little is known about the nuclear activity of MMPs or how MMPs are shuttling through different cellular compartments. In Xenopus laevis embryos, MMP28 is expressed in cranial placodes which are located lateral to the very motile neural crest (NC) cells, and later persists in the epibranchial placodes between the migrating streams of cranial NC cells. Interestingly, our preliminary results show that MMP28 secreted by cranial placodes is detected in the nuclei of neighboring NC cells. MMP28 knockdown experiments demonstrate that nuclear MMP28 activity is essential to trigger EMT and NC collective cell migration both in vivo and in vitro. The discovery of this non-canonical/nuclear activity of MMP28 is paradigm shifting in the MMP field. However, it is still unclear whether MMP28 function in the NC is restricted to this nuclear activity and whether MMP28 has a more conventional activity as well. Furthermore, the mechanisms by which MMP28 is internalized by NC cells and eventually shuttles to the nucleus are not known. In this application we propose to address these questions by, i) assessing how MMP28 modulates EMT and NC cells migration, and impacts the coordinated collective migration of both placode and NC cells; ii) uncovering the mechanisms controlling MMP28 trafficking from the extracellular compartment into the nucleus. The project has the strong potential to reveal novel aspects of MMPs functions, and their roles in the control of migratory cell behaviour in normal and pathological situations.

Public Health Relevance

Matrix metalloproteinase 28 (MMP28) belongs to a family of enzymes primarily known for their activity at the cell surface during development, and in a number of diseases including cancer. In the embryo, MMP28 is essential for formation of the neural crest, a structure that gives rise to the head skeleton and most of the peripheral nervous system, however its activity is required in the neural crest cell nucleus. The goals of this application are to dissect the cellular and molecular mechanisms by which nuclear MMP28 regulates neural crest formation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21DE029333-01
Application #
9877032
Study Section
Intercellular Interactions Study Section (ICI)
Program Officer
Stein, Kathryn K
Project Start
2019-12-15
Project End
2021-11-30
Budget Start
2019-12-15
Budget End
2020-11-30
Support Year
1
Fiscal Year
2020
Total Cost
Indirect Cost
Name
New York University
Department
Other Basic Sciences
Type
Schools of Dentistry/Oral Hygn
DUNS #
041968306
City
New York
State
NY
Country
United States
Zip Code
10012