Research Group

Louise Cramer Research Group

1987 BSc Imperial College London
1991 PhD Imperial College London
Louise Cramer
Tel: 020 7679 7260 (office)
Tel: 020 7679 7264 (lab)
Fax: 020 7679 7805
1991 Human Frontiers Fellow
1994 American Cancer Society Senior Fellow
1998 Wellcome Trust Career development award
1999-2008 Royal Society University Research Fellowship
2002 Royal Society URF merit award
Previous Posts: 
1991-1997 Postdoctoral Fellow University of California San Francisco, San Francisco USA
1997-1998 Postdoc, Kings College London

actin filament organization in a migrating fibroblast

The Cramer laboratory studies cytoskeleton mechanisms in cell polarity and cell migration. Cell migration is essential for life; required throughout embryo development, and for tissue repair and immunity in both the embryo and the adult. It also contributes to several important diseases, including inflammatory diseases, mental retardation and the spread of cancer. Determining molecular mechanisms controlling cell migration thus promises to provide effective therapeutic strategies for treating disease. We are interested in how migrating cells reach new territory and how they polarize to activate motility. We focus on determining actin cytoskeleton-based mechanical forces that drive these processes analysed at high spatiotemporal resolution, mainly using primary fibroblasts as model systems.



Establishment of Cell Polarity


Model for how cells initiate cell polarization from the cell front and cell rear.

To initiate directed migration a cell must break cell symmetry and form a
cell front and cell back, at opposing ends of the cell along an axis
approximately aligned with the direction of locomotion. In the main,
actin-based mechanical forces first shape - and then propel - the cell
front and cell rear forwards in the direction of migration. We recently
discovered that constitutive cell migration is initiated from the cell
rear, not the cell front, the common view. Our findings provide a new
perspective on how cells polarize. To determine precise mechanism, we
are currently investigating the precise temporal order and spatial
organization of actin-based mechanical forces likely to be important for
triggering initial breaking of cell symmetry from the cell rear.



Ratio of actin monomer and actin filaments in a migrating fibroblast.

collaboration with Prof. Jim Bamburg’s lab at Colorado State University
we were the first to identify that actin depolymerization and the
ADF/cofilin family of proteins that regulate actin depolymerization are
necessary for cell polarization in migrating cells. This was
subsequently also discovered for several other migrating cell types by
other labs, thus increasingly revealing the importance of these proteins
for triggering migration. Our current endeavours focus on our finding
that ADF/cofilin controls the formation of oriented actomyosin II
bundles in the cell body that in turn specifies the formation of the
front and back of the cell around the ends of the bundles during cell
polarization. We are investigating the mechanism of formation of
oriented actin bundles and the spatiotemporal regulation of ADF/cofilin
in triggering polarization and maintaining migration.

We found that the ratio of monomer:polymer is low (blue) within the
cell front. Consistent with this, we also discovered that actin
filaments are immediately recycled (depolymerised) to provide monomer
fuel to sustain actin polymerization-driven cell protrusion in migrating