2. Academic Validation
  3. ERM-dependent movement of CD43 defines a novel protein complex distal to the immunological synapse

ERM-dependent movement of CD43 defines a novel protein complex distal to the immunological synapse

  • Immunity. 2001 Nov;15(5):739-50. doi: 10.1016/s1074-7613(01)00224-2.
E J Allenspach 1,  P Cullinan,  J Tong,  Q Tang,  A G Tesciuba,  J L Cannon,  S M Takahashi,  R Morgan,  J K Burkhardt,  A I Sperling
Affiliations

Affiliation

  • 1 Section of Pulmonary and Critical Care Medicine, Department of Medicine, University of Chicago, Chicago, IL 60637, USA.
PMID: 11728336 DOI: 10.1016/s1074-7613(01)00224-2
Abstract

The large Mucin CD43 is actively excluded from T cell/APC interaction sites, concentrating in a membrane domain distal to the site of TCR engagement. The cytoplasmic region of CD43 was necessary and sufficient for this antipodal movement. ERM cytoskeletal adaptor proteins colocalized with CD43 in this domain. An ERM dominant-negative mutant blocked the distal accumulation of CD43 and another known ERM binding protein, Rho-GDI. Inhibition of ERM function decreased the production of IL-2 and IFNgamma, without affecting PKC(theta) focusing or CD69 upregulation. These results indicate that ERM proteins organize a complex distal to the T cell/APC interaction site and provide evidence that full T cell activation may involve removal of inhibitory proteins from the immunological synapse.

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