Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2020 Aug 18;9(8):234.
doi: 10.3390/biology9080234.

Conservation of Cell Communication Systems in Invertebrate Host-Defence Mechanisms: Possible Role in Immunity and Disease

Affiliations
Review

Conservation of Cell Communication Systems in Invertebrate Host-Defence Mechanisms: Possible Role in Immunity and Disease

Manon Auguste et al. Biology (Basel). .

Abstract

Innate immunity is continuously revealing multiple and highly conserved host-defence mechanisms. Studies on mammalian immunocytes are showing different communication systems that may play a role in coordinating innate immune responses also in invertebrates. Extracellular traps (ETs) are an immune response by which cells release net-like material, including DNA, histones and proteins. ETs are thought to immobilise and kill microorganisms, but are also involved in inflammation and autoimmune disease. Immune cells are also known to communicate through extracellular vesicles secreted in the extracellular environment or exosomes, which can carry a variety of different signalling molecules. Tunnelling nanotubes (TNTs) represent a direct cell-to-cell communication over a long distance, that allow for bi- or uni-directional transfer of cellular components between cells. Their functional role in a number of physio-pathological processes, including immune responses and pathogen transfer, has been underlined. Although ETs, exosomes, and TNTs have been described in invertebrate species, their possible role in immune responses is not fully understood. In this work, available data on these communication systems are summarised, in an attempt to provide basic information for further studies on their relevance in invertebrate immunity and disease.

Keywords: cell communication; exosomes; extracellular traps; innate immunity; invertebrates; tunnelling nanotubes.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Different cell structures that allow cells to communicate and perform diverse roles in host defence and homeostasis. Top: Extracellular Traps (ETosis), Middle: Exosome release, Bottom: Tunnelling nanotubes (TNTs).
Figure 2
Figure 2
TNT-like structures between the haemocytes of M. galloprovincialis observed with different stainings. (A) fixed haemocytes stained with Giemsa; live haemocytes stained with Neutral Red (NR) for lysosomes (B), and with the Fluorescent dye Tetramethylrhodamine ethyl ester perchlorate (TMRE), fro mitochondria (C). See Supplementary Materials for details. Scale bar: 20 µm.

References

    1. Brinkmann V., Reichard U., Goosmann C., Fauler B., Uhlemann Y., Weiss D.S., Weinrauch Y., Zychlinsky A. Neutrophil extracellular traps kill bacteria. Science. 2004;303:1532–1535. doi: 10.1126/science.1092385. - DOI - PubMed
    1. Stoiber W., Obermayer A., Steinbacher P., Krautgartner W.D. The role of reactive oxygen species (ROS) in the formation of Extracellular Traps (ETs) in humans. Biomolecules. 2015;5:702–723. doi: 10.3390/biom5020702. - DOI - PMC - PubMed
    1. Ravindran M., Khan M.A., Palaniyar N. Neutrophil extracellular trap formation: Physiology, pathology, and pharmacology. Biomolecules. 2019;9:365. doi: 10.3390/biom9080365. - DOI - PMC - PubMed
    1. Liang X., Liu L., Wang Y., Guo H., Fan H., Zhang C., Hou L., Liu Z. Autophagy-driven NETosis is a double-edged sword. Biomed. Pharmacother. 2020;126:110065. doi: 10.1016/j.biopha.2020.110065. - DOI - PubMed
    1. Hamam H.J., Palanyar N. Post-translational modifications in NETosis and NETs-mediated diseases. Biomolecules. 2019;9:369. doi: 10.3390/biom9080369. - DOI - PMC - PubMed

LinkOut - more resources