Masumi Eto, PhD
Philadelphia, PA 19107
(215) 503-2073 fax
Most Recent Peer-reviewed Publications
- F-actin clustering and cell dysmotility induced by the pathological W148R missense mutation of filamin B at the actin-binding domain
- Reconstituted human myosin light chain phosphatase reveals distinct roles of two inhibitory phosphorylation sites of the regulatory subunit, MYPT1
- Nuclear localization of CPI-17, a protein phosphatase-1 inhibitor protein, affects histone H3 phosphorylation and corresponds to proliferation of cancer and smooth muscle cells
- Endogenous inhibitor proteins that connect Ser/Thr kinases and phosphatases in cell signaling
- Caffeine relaxes smooth muscle through actin depolymerization
PhD, Hokkaido University, Chemistry - 1996
Expertise & Research Interests
PHOSPHATASE SIGNALING IN REGULATION OF CELL MOTILITY
The long-term goal of our research is to understand signal transduction controlling cell motility, a fundamental process for every aspect in biology. Environmental cues, such as released chemical substances and physical stresses, trigger reorganization of cytoskeletons, resulting in force generation, morphological change, transportation, and migration. Signals controlling cell motility are dynamic and orchestrated in TIME and SPACE. Not surprisingly, dysfunctions in the cytoskeletal reorganization have been linked to various diseases, as well as served as a therapeutic target to normalize pathological situations.
Our research focus involves roles of protein phosphatases in the regulation of cell motility. For example, smooth muscle contraction is controlled through the phosphorylation of myosin, a motor protein. Agonist stimulation activates G-proteins, resulting in an enhance in kinase in parallel to the inhibition of phosphatase. The inhibition of phosphatase is necessary for robust and sustained myosin phosphorylation and force generation. In general, multiple regulatory elements are involved in cellular phosphatase regulation, while a limited knowledge of the mechanisms controlling phosphatase activity is currently available.
We use a multidisciplinary approach, including techniques in biochemistry, cell biology, structural biology and physiology, to understand spatio-temporal regulation of cell motility via phosphatases. Our works uncovered a novel family of endogenous phosphatase inhibitor proteins that mediate kinase signal into phosphatase. These are highlights of our research:
- Understanding of spatio-temporal regulation of protein phosphatases that control cell motility, neuronal transmission, cancer cell migration and cytokinesis.
FASEB J. 2003, J Biol. Chem. 2001, 2002, 2007, Neuron 2002, J Cell Sci. 2002, 2006, Cell Motil. Cytoskel. 2000, 2005
- Characterization of signal transduction controlling agonist-induced smooth muscle contraction and relaxation.
J. Biol. Chem. 2000, 2001, 2009, Circ. Res. 2007, J. Physiol. 2009
- Structural sights into regulation of protein phosphatases.
J Mol Biol 2001, 2002, PNAS 2003, Structure 2007
Previous Lab Members
- Archana Verma, Postdoc Fellow
- Jason A. Kirkbride, Senior Research Associate
- Shawna Dougherty, MS student
- Yongtong Zhao, Senior Research Associate
- Jee In Kim, Postdoc Fellow
- Garbo D. Young, Lab Specialist/MS student
- Mark Urban, Lab Specialist
- Mukta Khasnis, Lab Specialist/MS student
- Kristyn Gummper, Lab Specialist/MS Student
- Nana Karikari, MS Student
Cell motility; Smooth muscle contraction; Artery; Airway; Hypertension; Asthma; Cancer; Signal Transduction; G-protein; Myosin; Phosphorylation; Cytoskeleton; Protein Kinase C; Rho-kinase; Myosin Phosphatase; Protein Phosphatase; CPI-17; PHI-1; Filamin; STAT3; ERK1/2; Enzyme regulation; Cell Imaging; Fluorescence microscope; FRET imaging; Fluorescence Polarization; Structural biology; NMR spectroscopy; Computer modeling; Proteome; Phosphatome; Protein purification; Yeast two-hybrid; Molecular Physiology; Vascular Biology; Biochemistry; Cell Biology