Organ-organ communication: The liver's perspective

Theranostics. 2021 Jan 16;11(7):3317-3330. doi: 10.7150/thno.55795. eCollection 2021.

Abstract

Communication between organs participates in most physiological and pathological events. Owing to the importance of precise coordination among the liver and virtually all organs in the body for the maintenance of homeostasis, many hepatic disorders originate from impaired organ-organ communication, resulting in concomitant pathological phenotypes of distant organs. Hepatokines are proteins that are predominantly secreted from the liver, and many hepatokines and several signaling proteins have been linked to diseases of other organs, such as the heart, muscle, bone, and eyes. Although liver-centered interorgan communication has been proposed in both basic and clinical studies, to date, the regulatory mechanisms of hepatokine production, secretion, and reciprocation with signaling factors from other organs are obscure. Whether other hormones and cytokines are involved in such communication also warrants investigation. Herein, we summarize the current knowledge of organ-organ communication phenotypes in a variety of diseases and the possible involvement of hepatokines and/or other important signaling factors. This provides novel insight into the underlying roles and mechanisms of liver-originated signal transduction and, more importantly, the understanding of disease in an integrative view.

Keywords: Cytokine; Disease mechanism.; Hepatokine; Liver; Organ communication.

Publication types

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

MeSH terms

  • Angiotensinogen / genetics
  • Angiotensinogen / metabolism*
  • Animals
  • Bone and Bones / metabolism
  • Brain / metabolism
  • Cytokines / genetics
  • Cytokines / metabolism*
  • Eye / metabolism
  • Fetuins / genetics
  • Fetuins / metabolism*
  • Fibroblast Growth Factors / genetics
  • Fibroblast Growth Factors / metabolism*
  • Gene Expression Regulation
  • Humans
  • Intercellular Signaling Peptides and Proteins / genetics
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • Kidney / metabolism
  • Liver / metabolism*
  • Lung / metabolism
  • Muscle, Skeletal / metabolism
  • Myocardium / metabolism
  • Proteoglycans / genetics
  • Proteoglycans / metabolism*
  • Signal Transduction

Substances

  • Cytokines
  • Enho protein, human
  • FGF21 protein, human
  • Fetuins
  • Intercellular Signaling Peptides and Proteins
  • Proteoglycans
  • TSKU protein, human
  • Angiotensinogen
  • Fibroblast Growth Factors