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Updated: May 18, 2026

Imaging the Human Immunological Synapse
Published on: December 26, 2019
Cell polarisation and the immunological synapse
Karen L Angus1, Gillian M Griffiths
1Cambridge Institute for Medical Research, Addenbrooke's Hospital, Cambridge, CB2 0XY, England, UK.
Insights
Immune cells form an immunological synapse (IS) to direct secretion, requiring cell polarity. Novel findings reveal protein roles in centrosome relocation and actin networks enabling exocytosis during IS formation.
Area of Science:
- Immunology
- Cell Biology
- Biophysics
Background:
- Directed secretion by immune cells necessitates the formation of the immunological synapse (IS) at cell-cell contact sites.
- This process is accompanied by a significant induction of cell polarity.
Purpose of the Study:
- To discuss recent findings advancing the understanding of immunological synapse formation.
- To explore the mechanisms underlying induced cell polarity in immune cells.
Main Methods:
- Super-resolution imaging techniques were employed.
- Identification of specific proteins involved in centrosome regulation.
Main Results:
- A protein regulating centrosome relocation to the plasma membrane was identified.
- Super-resolution imaging revealed a residual actin network at the IS, potentially facilitating secretory granule exocytosis.
- Parallels were drawn between primary cilia and IS architecture.
Conclusions:
- Novel findings have significantly advanced the understanding of IS formation.
- These insights contribute to comprehending induced cell polarity in immune cells during directed secretion.
Abstract:
Directed secretion by immune cells requires formation of the immunological synapse at the site of cell-cell contact, concomitant with a dramatic induction of cell polarity. Recent findings provide us with insights into the various steps that are required for these processes: for example, the first identification of a protein at the centrosome that regulates its relocation to the plasma membrane; the use of super-resolution imaging techniques to reveal a residual actin network at the immunological synapse that may permit secretory granule exocytosis; and the drawing of parallels between primary cilia and IS architecture. Here we discuss these and other novel findings that have advanced our understanding of the complex process of immunological synapse formation and subsequent induced cell polarity in immune cells.
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