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Updated: May 27, 2026

Studying Organelle Dynamics in B Cells During Immune Synapse Formation
Published on: June 1, 2019
Lymphocyte polarity, the immunological synapse and the scope of biological analogy
1Immunology Program; Memorial Sloan-Kettering Cancer Center; New York, NY USA.
Insights
Diacylglycerol, a lipid molecule, is essential for microtubule-organizing center (MTOC) reorientation in T cells. This process is vital for immune cell communication and function at the immunological synapse.
Area of Science:
- Immunology
- Cell Biology
- Cytoskeletal Dynamics
Background:
- Lymphocytes form immunological synapses for intercellular communication and killing.
- Microtubule-organizing center (MTOC) polarization is critical for directional secretion at the synapse.
- Studying MTOC reorientation in lymphocytes has been technically challenging.
Purpose of the Study:
- To investigate the molecular mechanisms underlying MTOC reorientation in T cells.
- To elucidate the role of lipid second messengers in lymphocyte polarity.
- To develop novel methods for analyzing cytoskeletal dynamics during synapse formation.
Main Methods:
- Developed a photoactivation and imaging strategy for high-resolution analysis of T cell cytoskeletal dynamics.
- Investigated the recruitment of protein kinase C (PKC) family members to the synapse.
- Examined the role of diacylglycerol in MTOC reorientation.
Main Results:
- Demonstrated that diacylglycerol is crucial for MTOC reorientation.
- Showed that diacylglycerol promotes MTOC reorientation by recruiting PKC family members to the immunological synapse.
- Proposed a two-step model for MTOC reorientation in lymphocytes.
Conclusions:
- Diacylglycerol signaling is a key regulator of MTOC reorientation in T cells.
- Understanding lymphocyte polarity provides insights into broader cell polarity mechanisms.
- The developed imaging strategy enables detailed analysis of cytoskeletal dynamics in immune cells.
Abstract:
Lymphocytes such as T cells, B cells and natural killer (NK) cells form specialized contacts, called immunological synapses, with other cells in order to engage in specific intercellular communication and killing. Synapse formation is associated with the polarization of the microtubule-organizing center (MTOC) toward the contact site, which enables the directional secretion of cytokines and lytic factors. Although MTOC reorientation to the synapse is crucial for lymphocyte function, it has been difficult to study because of technical constraints. We have developed a photoactivation and imaging strategy that enables high-resolution analysis of cytoskeletal dynamics in individual T cells. Using this approach, we have demonstrated that the lipid second messenger diacylglycerol plays a crucial role in promoting MTOC reorientation by recruiting three members of the protein kinase C family to the synapse. Here, I will discuss these results along with studies from other labs, which have explored the role of polarity-inducing protein complexes after synapse formation. I will also propose a two-step model for MTOC reorientation in lymphocytes that reflects what we now know about the subject. Finally, I will consider the extent to which lymphocyte polarity resembles analogous cell polarity systems in other cell types.
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