Reciprocal TCR-CD3 and CD4 Engagement of a Nucleating pMHCII Stabilizes a Functional Receptor Macrocomplex

Caleb R. Glassman, Heather L. Parrish, Mark S. Lee, Michael S Kuhns

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

CD4+ T cells convert the time that T cell receptors (TCRs) interact with peptides embedded within class II major histocompatibility complex molecules (pMHCII) into signals that direct cell-fate decisions. In principle, TCRs relay information to intracellular signaling motifs of the associated CD3 subunits, while CD4 recruits the kinase Lck to those motifs upon coincident detection of pMHCII. But the mechanics by which this occurs remain enigmatic. In one model, the TCR and CD4 bind pMHCII independently, while in another, CD4 interacts with a composite surface formed by the TCR-CD3 complex bound to pMHCII. Here, we report that the duration of TCR-pMHCII interactions impact CD4 binding to MHCII. In turn, CD4 increases TCR confinement to pMHCII via reciprocal interactions involving membrane distal and proximal CD4 ectodomains. The data suggest that a precisely assembled macrocomplex functions to reliably convert TCR-pMHCII confinement into reproducible signals that orchestrate adaptive immunity. Glassman, Parrish et al. use functional and biophysical assays to demonstrate that CD4 stabilizes TCR-pMHCII interactions via membrane distal and proximal domains. The data indicate that CD4 docks along a composite surface created by the TCR-CD3-pMHCII axis to confer a uniform macrocomplex architecture upon a diverse TCR repertoire.

Original languageEnglish (US)
Pages (from-to)1263-1275
Number of pages13
JournalCell Reports
Volume22
Issue number5
DOIs
StatePublished - Jan 30 2018
Externally publishedYes

Fingerprint

T-Cell Antigen Receptor
Lymphocyte Specific Protein Tyrosine Kinase p56(lck)
CD3 Antigens
Membranes
Docks
T-cells
Composite materials
Adaptive Immunity
Major Histocompatibility Complex
Mechanics
Assays
T-Lymphocytes
Peptides
Molecules

Keywords

  • CD3
  • CD4
  • pMHCII
  • T cell
  • TCR

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)

Cite this

Reciprocal TCR-CD3 and CD4 Engagement of a Nucleating pMHCII Stabilizes a Functional Receptor Macrocomplex. / Glassman, Caleb R.; Parrish, Heather L.; Lee, Mark S.; Kuhns, Michael S.

In: Cell Reports, Vol. 22, No. 5, 30.01.2018, p. 1263-1275.

Research output: Contribution to journalArticle

Glassman, Caleb R. ; Parrish, Heather L. ; Lee, Mark S. ; Kuhns, Michael S. / Reciprocal TCR-CD3 and CD4 Engagement of a Nucleating pMHCII Stabilizes a Functional Receptor Macrocomplex. In: Cell Reports. 2018 ; Vol. 22, No. 5. pp. 1263-1275.
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