The emerging role of extracellular vesicles as communicators between adipose tissue and pathologic lungs with a special focus on asthma

Am J Physiol Cell Physiol. 2023 May 1;324(5):C1119-C1125. doi: 10.1152/ajpcell.00057.2023. Epub 2023 Apr 17.

Abstract

Extracellular vesicles (EVs) gain increasing attention due to their (patho-)physiological role in intercellular signaling, specifically in the communication between distant organs. Recent studies highlight a connection between the adipose tissue (AT) and the lung via (immuno-)modulatory EVs in disorders such as obesity-associated asthma and lung cancer-associated cachexia. Although lung cancer-derived EVs induce lipolysis and myotube atrophy in vivo, pathogenic effects were also reported in the opposite direction with the involvement of AT-derived EVs in cancer-promoting responses and potentially in asthma development. In contrast, the majority of studies on AT-derived EVs demonstrate their protective influence on the asthmatic lung. Beneficial effects, such as induction of anti-inflammatory pathways in vitro and in ovalbumin (OVA)-induced asthma mouse models, were particularly conveyed by EVs enriched from AT-derived mesenchymal stem/stromal cells (AT-MSCs), which therefore pose an interesting subject in possible future therapeutic applications. Likewise, AT-MSC-derived EVs exerted beneficial effects in several other pulmonary abnormalities, such as different types of lung injury or pathological changes related to chronic obstructive pulmonary disease. These contradictory findings highlight the need for extensive research to widen the understanding of the role of EVs in the development of diseases and interconnectivity between organs.

Keywords: adipose tissue (AT); adipose tissue-derived mesenchymal stem/stromal cells (AT-MSCs); asthma; extracellular vesicles (EVs); lung disorders.

Publication types

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

MeSH terms

  • Adipose Tissue / pathology
  • Animals
  • Asthma* / metabolism
  • Asthma* / pathology
  • Asthma* / therapy
  • Extracellular Vesicles* / metabolism
  • Lung / pathology
  • Lung Neoplasms* / metabolism
  • Mice