4.5 Review

Intercellular communication lessons in heart failure

Journal

EUROPEAN JOURNAL OF HEART FAILURE
Volume 17, Issue 11, Pages 1091-1103

Publisher

WILEY
DOI: 10.1002/ejhf.399

Keywords

Heart failure; cell-cell communication; inter-organ communication; paracrine signalling mediators

Funding

  1. Integrated Research and Treatment Centre, BMBF
  2. Deutsche Forschungsgemeinschaft [DFG TH903/10-1]
  3. 7th European Framework programme (FIBROTARGET)
  4. HRCMM (Heidelberg Research Centre for Molecular Medicine) Career Development Fellowship
  5. European Commission 7th Framework Programme (EUTrigTreat)
  6. Telethon Foundation [GGP11224]
  7. Swedish Research Council
  8. Swedish Heart and Lung Foundation
  9. Diabetes Foundation
  10. Karolinska Institutet
  11. Swedish Society for Medical Research
  12. EMBO Longterm Fellowship
  13. European Commission (EMBOCOFUND) - Marie Curie Actions [GA-210-267146]
  14. European Commission (FP7-Health) [MEDIA-261409]
  15. British Heart Foundation [PG/13/56/30383]
  16. Oxford Biomedical Research Council
  17. Marie Curie Intra-European Fellowship by the European Commission within FP7 (HRS-EAT) [300289]
  18. Deutsche Forschungsgemeinschaft DFG [SP-1293/1-1]
  19. European Commission7th Framework Programme (SysKid)
  20. Else-Kroener-Fresenius foundation
  21. British Heart Foundation [FS/11/66/28855, PG/13/56/30383] Funding Source: researchfish

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Cell-cell or inter-organ communication allows the exchange of information and messages, which is essential for the coordination of cell/organ functions and the maintenance of homeostasis. It has become evident that dynamic interactions of different cell types play a major role in the heart, in particular during the progression of heart failure, a leading cause of mortality worldwide. Heart failure is associated with compensatory structural and functional changes mostly in cardiomyocytes and cardiac fibroblasts, which finally lead to cardiomyocyte hypertrophy and fibrosis. Intercellular communication within the heart is mediated mostly via direct cell-cell interaction or the release of paracrine signalling mediators such as cytokines and chemokines. However, recent studies have focused on the exchange of genetic information via the packaging into vesicles as well as the crosstalk of lipids and other paracrine molecules within the heart and distant organs, such as kidney and adipose tissue, which might all contribute to the pathogenesis of heart failure. In this review, we discuss emerging communication networks and respective underlying mechanisms which could be involved in cardiovascular disease conditions and further emphasize promising therapeutic targets for drug development.

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