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Updated: May 17, 2026

Visualizing the Actin and Microtubule Cytoskeletons at the B-cell Immune Synapse Using Stimulated Emission Depletion (STED) Microscopy
Published on: April 9, 2018
Microtubule-organizing center polarity and the immunological synapse: protein kinase C and beyond
1Immunology Program, Memorial Sloan-Kettering Cancer Center , New York, NY, USA.
Insights
Cytoskeletal polarization guides immune cell interactions. Recent findings reveal protein kinase C family members are key regulators of the microtubule-organizing center (MTOC) polarization essential for T cell responses.
Area of Science:
- Immunology
- Cell Biology
- Molecular Biology
Background:
- Cytoskeletal polarization is vital for immune cell functions, including neutrophil migration and T cell-APC interactions.
- The immunological synapse (IS) involves T cell microtubule-organizing center (MTOC) reorientation for directed effector molecule release.
Purpose of the Study:
- To review recent advances in understanding the mechanisms of MTOC polarization during T cell activation.
- To highlight the role of protein kinase C (PKC) family members in establishing and maintaining cytoskeletal polarity.
Main Methods:
- Literature review of recent studies on T cell signaling and cytoskeletal dynamics.
- Focus on molecular mechanisms linking T cell receptor (TCR) signaling to MTOC polarization.
Main Results:
- TCR stimulation triggers MTOC polarization, crucial for specific T cell responses.
- Novel and atypical protein kinase C (PKC) family members are identified as critical regulators of MTOC polarization.
Conclusions:
- Understanding MTOC polarization machinery is key to deciphering T cell effector functions.
- PKC family members represent important targets for modulating T cell-mediated immunity.
Abstract:
Cytoskeletal polarization is crucial for many aspects of immune function, ranging from neutrophil migration to the sampling of gut flora by intestinal dendritic cells. It also plays a key role during lymphocyte cell-cell interactions, the most conspicuous of which is perhaps the immunological synapse (IS) formed between a T cell and an antigen-presenting cell (APC). IS formation is associated with the reorientation of the T cell's microtubule-organizing center (MTOC) to a position just beneath the cell-cell interface. This cytoskeletal remodeling event aligns secretory organelles inside the T cell with the IS, enabling the directional release of cytokines and cytolytic factors toward the APC. MTOC polarization is therefore crucial for maintaining the specificity of a T cell's secretory and cytotoxic responses. It has been known for some time that T cell receptor (TCR) stimulation activates the MTOC polarization response. It has been difficult, however, to identify the machinery that couples early TCR signaling to cytoskeletal remodeling. Over the past few years, considerable progress has been made in this area. This review will present an overview of recent advances, touching on both the mechanisms that drive MTOC polarization and the effector responses that require it. Particular attention will be paid to both novel and atypical members of the protein kinase C family, which are now known to play important roles in both the establishment and the maintenance of the polarized state.
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