Hippo Pathway in Mammalian Adaptive Immune System

Cells. 2019 Apr 30;8(5):398. doi: 10.3390/cells8050398.

Abstract

The Hippo pathway was originally identified as an evolutionarily-conserved signaling mechanism that contributes to the control of organ size. It was then rapidly expanded as a key pathway in the regulation of tissue development, regeneration, and cancer pathogenesis. The increasing amount of evidence in recent years has also connected this pathway to the regulation of innate and adaptive immune responses. Notably, the Hippo pathway has been revealed to play a pivotal role in adaptive immune cell lineages, as represented by the patients with T- and B-cell lymphopenia exhibiting defective expressions of the pathway component. The complex regulatory mechanisms of and by the Hippo pathway have also been evident as alternative signal transductions are employed in some immune cell types. In this review article, we summarize the current understanding of the emerging roles of the Hippo pathway in adaptive immune cell development and differentiation. We also highlight the recent findings concerning the dual functions of the Hippo pathway in autoimmunity and anti-cancer immune responses and discuss the key open questions in the interplay between the Hippo pathway and the mammalian immune system.

Keywords: Hippo pathway; LATS (large tumor suppressor kinase); MST (mammalian STE20-like protein kinase); TAZ (transcriptional co-activator with PDZ-binding motif); YAP (yes-associated protein); adaptive immunity; autoimmunity; cancer immunity; innate immunity.

Publication types

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

MeSH terms

  • Adaptive Immunity / immunology*
  • Animals
  • Autoimmunity / immunology*
  • Cell Differentiation / immunology
  • Drosophila / metabolism
  • Humans
  • Lymphopenia / immunology*
  • Mammals / immunology*
  • Neoplasms / immunology*
  • Protein Serine-Threonine Kinases / immunology*
  • Signal Transduction*
  • T-Lymphocytes / cytology
  • T-Lymphocytes / immunology

Substances

  • Protein Serine-Threonine Kinases