Supramolecular attack particles are autonomous killing entities released from cytotoxic T cells

Author:

Bálint Š.1ORCID,Müller S.2ORCID,Fischer R.3ORCID,Kessler B. M.3ORCID,Harkiolaki M.4ORCID,Valitutti S.25ORCID,Dustin M. L.1ORCID

Affiliation:

1. Kennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.

2. Cancer Research Center of Toulouse, INSERM, Toulouse, France.

3. Discovery Proteomics Facility, Target Discovery Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.

4. Diamond Light Source, Harwell Science and Innovation Campus, Chilton, Didcot, UK.

5. Department of Pathology, Institut Universitaire du Cancer-Oncopole, Toulouse, France.

Abstract

Supramolecular attack particles Cytotoxic T cells (CTLs) are at the front lines against cancer and chronic infection. T cells kill by secreting caspase-activating granzymes and the pore-forming protein perforin from dense core granules. However, the structural basis of lethal hit delivery has remained unknown. Balint et al. enriched the synaptic output of CTLs to investigate the released form of perforin and granzyme B. They found that CTLs released perforin and granzymes in stable particles called supramolecular attack complexes or SMAPs. The SMAPs were composed of a core shell structure and were assembled in the CTL dense secretory granules before release. The released SMAPs showed an innate ability to kill target cells. Science , this issue p. 897

Funder

Wellcome Trust Centre for Mitochondrial Research

Ligue Nationale contre le Cancer

Kennedy Trust

ERC AdG

Laboratoire d’Excellence Toulouse Cancer

Institute for Protein Innovation

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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