C-type lectin domain group 14 proteins in vascular biology, cancer and inflammation

FEBS J. 2019 Sep;286(17):3299-3332. doi: 10.1111/febs.14985. Epub 2019 Jul 29.

Abstract

The C-type lectin domain (CTLD) group 14 family of transmembrane glycoproteins consist of thrombomodulin, CD93, CLEC14A and CD248 (endosialin or tumour endothelial marker-1). These cell surface proteins exhibit similar ectodomain architecture and yet mediate a diverse range of cellular functions, including but not restricted to angiogenesis, inflammation and cell adhesion. Thrombomodulin, CD93 and CLEC14A can be expressed by endothelial cells, whereas CD248 is expressed by vasculature associated pericytes, activated fibroblasts and tumour cells among other cell types. In this article, we review the current literature of these family members including their expression profiles, interacting partners, as well as established and speculated functions. We focus primarily on their roles in the vasculature and inflammation as well as their contributions to tumour immunology. The CTLD group 14 family shares several characteristic features including their ability to be proteolytically cleaved and engagement of some shared extracellular matrix ligands. Each family member has strong links to tumour development and in particular CD93, CLEC14A and CD248 have been proposed as attractive candidate targets for cancer therapy.

Keywords: C-type lectin; CD248; CD93; CLEC14A; cancer; extracellular matrix; group XIV; immuno-oncology; thrombomodulin; vascular targeting.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antigens, CD / genetics
  • Antigens, CD / metabolism*
  • Antigens, Neoplasm / genetics
  • Antigens, Neoplasm / metabolism*
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / metabolism*
  • Endothelium, Vascular / metabolism*
  • Humans
  • Lectins, C-Type / genetics
  • Lectins, C-Type / metabolism*
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism*
  • Neoplasms / metabolism
  • Neovascularization, Physiologic
  • Receptors, Complement / genetics
  • Receptors, Complement / metabolism*
  • Thrombomodulin / genetics
  • Thrombomodulin / metabolism*

Substances

  • Antigens, CD
  • Antigens, Neoplasm
  • CD248 protein, human
  • CLEC14A protein, human
  • Cell Adhesion Molecules
  • Lectins, C-Type
  • Membrane Glycoproteins
  • Receptors, Complement
  • Thrombomodulin
  • complement 1q receptor