Cell-cell interactions are of critical importance for expanding the range of the immune response in order to control infection. Yet, the mechanisms that control cell-cell contacts and receptor movement in the immune system remain cryptic. Using high-speed video microscopy, we have been able to demonstrate T cell receptor clustering followed by coalescence of these clusters into the central """"""""synapse"""""""". Through simultaneous imaging of intracellular calcium levels, it has become apparent that while initial microclusters are associated with the onset of signaling, a program of cellular re-polarization is necessary for the formation of the central synapse structure and for sustained signaling. The overall goal of my research is to define spatial and temporal maps of the initiating events of immune recognition. The hypothesis underlying this project is that cellular myosin motors triggered by initial TCR signals are crucial for polarization of key membrane receptors into signaling complexes.
The specific aims of this project are: 1. To define the myosin family members that are uniquely responsible for synapse formation in T cells, using biochemistry, in situ localization techniques and dominant negative mutations. 2. To determine the biochemical roles for myosins in T cell signaling by examining the interaction partners and phosphorylation of myosins upon TCR ligation. 3. To define the overlapping role of myosin-motors with signaling mediated by costimulatory signals and with signaling mediated by chemokines. These studies will not only provide fundamental information about the initial steps in lymphocyte activation, but may also lead to clues about ways to manipulate T cell responses in vitro and in vivo.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI052116-03
Application #
6696572
Study Section
Allergy and Immunology Study Section (ALY)
Program Officer
Nabavi, Nasrin N
Project Start
2002-09-15
Project End
2007-02-28
Budget Start
2004-03-01
Budget End
2005-02-28
Support Year
3
Fiscal Year
2004
Total Cost
$297,850
Indirect Cost
Name
University of California San Francisco
Department
Pathology
Type
Schools of Medicine
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Krummel, Matthew F; Mahale, Jagdish N; Uhl, Lion F K et al. (2018) Paracrine costimulation of IFN-? signaling by integrins modulates CD8 T cell differentiation. Proc Natl Acad Sci U S A 115:11585-11590
Cai, En; Marchuk, Kyle; Beemiller, Peter et al. (2017) Visualizing dynamic microvillar search and stabilization during ligand detection by T cells. Science 356:
Mujal, Adriana M; Gilden, Julia K; Gérard, Audrey et al. (2016) A septin requirement differentiates autonomous and contact-facilitated T cell proliferation. Nat Immunol 17:315-22
Krummel, Matthew F; Bartumeus, Frederic; Gérard, Audrey (2016) T cell migration, search strategies and mechanisms. Nat Rev Immunol 16:193-201
Pinkard, Henry; Stuurman, Nico; Corbin, Kaitlin et al. (2016) Micro-Magellan: open-source, sample-adaptive, acquisition software for optical microscopy. Nat Methods 13:807-809
Pinkard, Henry; Corbin, Kaitlin; Krummel, Matthew F (2016) Spatiotemporal Rank Filtering Improves Image Quality Compared to Frame Averaging in 2-Photon Laser Scanning Microscopy. PLoS One 11:e0150430
Mujal, Adriana M; Krummel, Matthew (2015) The subtle hands of self-reactivity in peripheral T cells. Nat Immunol 16:10-1
Krummel, Matthew F; Friedman, Rachel S; Jacobelli, Jordan (2014) Modes and mechanisms of T cell motility: roles for confinement and Myosin-IIA. Curr Opin Cell Biol 30:9-16
Corbin, Kaitlin; Pinkard, Henry; Peck, Sebastian et al. (2014) Assessing and benchmarking multiphoton microscopes for biologists. Methods Cell Biol 123:135-51
Gérard, Audrey; Patino-Lopez, Genaro; Beemiller, Peter et al. (2014) Detection of rare antigen-presenting cells through T cell-intrinsic meandering motility, mediated by Myo1g. Cell 158:492-505

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