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* These authors contributed equally
Corals create biodiverse ecosystems important for both humans and marine organisms. However, we still do not understand the full potential and function of many coral cells. Here, we present a protocol developed for the isolation, labeling, and separation of stony coral cell populations.
Coral reefs are under threat due to anthropogenic stressors. The biological response of coral to these stressors may occur at a cellular level, but the mechanisms are not well understood. To investigate coral response to stressors, we need tools for analyzing cellular responses. In particular, we need tools that facilitate the application of functional assays to better understand how cell populations are reacting to stress. In the current study, we use fluorescence-activated cell sorting (FACS) to isolate and separate different cell populations in stony corals. This protocol includes: (1) the separation of coral tissues from the skeleton, (2) creation of a single cell suspension, (3) labeling the coral cells using various markers for flow cytometry, and (4) gating and cell sorting strategies. This method will enable researchers to work on corals at the cellular level for analysis, functional assays, and gene expression studies of different cell populations.
Coral reefs are one of the most important ecosystems on Earth. They facilitate biodiversity by providing critical habitats for fish and invertebrates and are crucial for sustaining anthropogenic communities by providing food and economic livelihood through tourism1. As the key builder of coral reefs, the coral animal (Phylum: Cnidaria) also aids coastal communities by creating large calcium carbonate frameworks that mitigate wave and storm damage2.
Corals as adults are sessile animals that host a wide array of endosymbiotic partners, including viruses, archaea, bacteria, protists, fungi, and m....
1. Dissociation of tissues from coral skeleton via airbrush and compressor
NOTE: Perform steps on ice and protect hands with gloves.
Overall, this protocol is useful because it facilitates the identification and collection of live coral cell populations that can be used for functional analyses. The workflow started with the mechanical separation of coral tissues from the underlying calcium carbonate skeleton (Figure 1). This is one of the most important initial steps because improper technique results in high cell mortality and can create large amounts of debris. Enzymatic separation is no.......
This protocol was adapted from Rosental et al.18 and developed for the identification and isolation of P. damicornis cells. The methodology focuses on the process of filtering samples to remove debris, nonviable cells, and Symbiodiniaceae-hosted cells through the examination of cell intrinsic factors, including relative cell size, relative cell granularity, cell autofluorescence, and the presence of intact cellular membranes. These techniques can be applied to other coral species. However.......
NTK would like to acknowledge the University of Miami Research Awards in Natural Sciences and Engineering for funding this research. BR would like to thank Alex and Ann Lauterbach for funding the Comparative and Evolutionary Immunology Laboratory. The work of BR was supported by Israel Science Foundation (ISF) numbers: 1416/19 and 2841/19, and HFSP Research Grant, RGY0085/2019. We would like to thank Zhanna Kozhekbaeva and Mike Connelly for technical assistance. We would also like to thank the University of Miami, Miller School of Medicine’s Flow Cytometry Shared Resource at the Sylvester Comprehensive Cancer Center for access to the FACS cytometer and to S....
Name | Company | Catalog Number | Comments |
Airbrush Kit & Compressor | TCP Global | ABD KIT-H-SET | Paasche H Series Single-Action Siphon Feed Airbrush Kit with Master TC-20 Compressor & Air Hose |
BD FACSAria II | BD | 644832 | |
Bone Cutters | Bulk Reef Supply | 205357 | Oceans Wonders Coral Stony Bone Cutter |
Cell Strainer | Corning | 352340 | 40 um; BD Falcon; individually wrapped; sterile; nylon |
CellRox Green | Life Technologies | C10444 | 2.5 mM in DMSO; Excitation/Emission: 485/520 nm |
Collection bag | Grainger | 38UV35 | Reloc Zippit 6"L x 4"W Standard Reclosable Poly Bag with Zip Seal Closure, Clear; 2 mil Thickness |
DAPI | Invitrogen | D1306 | 10mg in H2O; Excitation/Emission: 358/461 nm |
Fetal Calf Serum | Sigma-Aldrich | F2442-100ML | Heat-inactivated at 57 °C for 30 minutes |
Hemacytometer | Sigma-Aldrich | Z359629 | Bright-Line Hemacytometer |
HEPES Buffer | Sigma-Aldrich | H0887 | |
LysoTracker Deep Red | Life Technologies | L12492 | 1mM in DMSO; Absorption/Emission: 647/668 nm |
Microcentrifuge tubes | VWR | 87003-294 | 1.7 mL |
Phophate Buffered Saline (PBS) | Gibco | 70011-044 | pH 7.4; 10X |
Round-bottom tubes | VWR | 352063 | 5 mL Polypropylene Round-Bottom Tube |
Syringe | BD | 309628 | 1 mL BD Luer-Lok Syringe sterile, singe use polycarbonate |
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