Co-option of immune and digestive cellular machinery to support photosymbiosis in amoebocytes of the upside-down jellyfish Cassiopea xamachana
Open Access
- 12 May 2025
- journal article
- Published by The Company of Biologists in Journal of Experimental Biology
- Vol. 228 (14)
Abstract
The upside-down jellyfish Cassiopea spp. host their algal symbionts inside a subset of amoebocytes, phagocytic cells that also play innate immune functions akin to macrophages from vertebrate animals. Amoebocyte precursors phagocytose algae from the jellyfish gut and store them inside intracellular compartments called symbiosomes. Subsequently, the precursors migrate to the mesoglea, differentiate into symbiotic amoebocytes, and roam throughout the jellyfish body, where the algae remain photosynthetically active and supply the jellyfish host with a significant portion of their organic carbon needs. Here, we show that the amoebocyte symbiosome membrane contains V-H+-ATPase (VHA), the proton pump that acidifies phagosomes and lysosomes in all eukaryotes. Many symbiotic amoebocytes also abundantly express a carbonic anhydrase (CA), an enzyme that reversibly hydrates CO2 into H+ and HCO3−. Moreover, we found that the symbiosome lumen is pronouncedly acidic and that pharmacological inhibition of VHA or CA activities significantly decreases photosynthetic oxygen production in live jellyfish. These results point to a carbon concentrating mechanism (CCM) that co-opts VHA and CA from the phago-lysosomal machinery that ubiquitously mediates food digestion and innate immune responses. Analogous VHA-dependent CCMs have been previously described in reef-building corals, anemones and giant clams; however, these other two cnidarians host their dinoflagellate algae inside gastrodermal cells – not in amoebocytes – and the clam hosts theirs within the gut lumen. Thus, our study identifies an example of convergent evolution at the cellular level that might broadly apply to invertebrate–microbe photosymbioses while also providing evolutionary links with intracellular and extracellular food digestion and the immune system.Keywords
Funding Information
- National Science Foundation (NSF-GRFP 2019271478)
- Scripps Institution of Oceanography
- Achievement Rewards for College Scientists Fellowship (NSF-GRFP 2023360321, 2316391)
- University of California, San Diego
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