The
molecular basis for cellular
contractility
Cellular
contractility via the Rho pathway plays essential roles
throughout the life of single- and multi-cellular
organisms. Rho-mediated contraction is essential during
cytokinesis to split a dividing cell into two daughters.
Rho is also important during cell migration to form
adhesions with the substrate and retract the cell’s
trailing edge. Contractile events are also required to
produce the forces that shape embryonic tissues during
early development and for tissue remodeling during wound
healing. Misregulation of the Rho pathway, however, has
more insidious effects and can lead to pathologies such as
hypertension, tissue inflammation, oncogenic
transformation, and tumor cell metastasis and angiogenesis.
Pharmaceutical intervention in Rho pathway signaling has
been used to successfully treat hypertension,
cardiovascular disorders, and to promote neuronal
regeneration. However, in order to extend the range of
treatment options that can target this pathway, we must
first identify all of the molecules involved and understand
how they interact as a system.
We
are using the Drosophila
gastrulation
pathway as a model system to study how cells perceive
signals from the external environment and convert them into
changes in cell shape. In flies, this pathway is activated
by the secreted protein Folded gastrulation (Fog). Fog is
a Drosophila
morphogen
that drives epithelial sheet remodeling during multiple
stages of embryogenesis. It's secreted by epithelial
tissues and acts as an autocrine signal to trigger cellular
contraction by activating the Rho pathway. Extracellular
Fog binds to an unknown receptor that activates the fly G
alpha12/13 subunit to stimulate RhoGEF2. RhoGEF2 activates
Rho which, in turn, stimulates myosin II via Rho-kinase. In
collaboration with Rich Superfine's lab
here at UNC, we are using state-of-the-art
microfabricated devices to measure forces produced by
actin-myosin contraction in Drosophila
cells
downstream of this signaling circuit.