IMAGE: A colony of Acropora tenuis grown in a natural sea environment and transferred to an aquarium to induce spawning.
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• Researchers have successfully grown cells from the stony coral, Acropora tenuis, in petri dishes
• The cell lines were created by separating out cells from coral larvae, which then developed into eight distinct cell types
• Seven out of eight cell types were stable and could grow indefinitely, remaining viable even after freezing
• Some of the cell types represented endoderm-like cells, and could therefore shed light on how coral interacts with photosynthesizing algae and how bleaching occurs
• The cell lines could be used in many avenues of coral cell research, including coral development, coral farming and the impact of climate change and pollution

Researchers in Japan have established sustainable cell lines in a coral, according to a study published today in Marine Biotechnology.

Seven out of eight cell cultures, seeded from the stony coral, Acropora tenuis, have continuously proliferated for over 10 months, the scientists reported.

“Establishing stable cells lines for marine organisms, especially coral, has proven very difficult in the past,” said Professor Satoh, senior author of the study and head of the Marine Genomics Unit at the Okinawa Institute of Science and Technology Graduate University (OIST). “This success could prove to be a pivotal moment for gaining a deeper understanding of the biology of these vitally important animals.”

Acropora tenuis belongs to the Acroporidae family, the most common type of coral found within tropical and subtropical reefs. These stony corals are fast growers and therefore play a crucial role in the structural formation of coral reefs.

However, Acroporidae corals are particularly susceptible to changes in ocean conditions, often undergoing bleaching events when temperatures soar or when oceans acidify. Establishing knowledge about the basic biology of these corals through cell lines could one day help protect them against climate change, explained Professor Satoh.

Creating the cultures

In the study, Professor Satoh worked closely with Professor Kaz Kawamura from Kochi University – an expert in developing and maintaining cell cultures of marine organisms.

Since adult coral host a wide variety of microscopic marine organisms, the group chose to try creating the cell lines from coral larvae to reduce the chances of cross-contamination. Another benefit of using larval cells was that they divide more easily than adult cells, potentially making them easier to culture.

The researchers used coral specimens in the lab to isolate both eggs and sperm and fertilize the eggs. Once the coral larvae developed, they separated the larvae into individual cells and grew them in petri dishes.

Initially, the culture attempts ended in failure. “Small bubble bodies appeared and then occupied most of the petri dish,” said Professor Kaz Kawamura. “We later found that these were the fragments of dying stony coral cells.”

In the second year, the group discovered that by adding a protease called plasmin to the cell culture medium, right at the beginning of the culture, they could stop the stony coral cells from dying and keep them growing.

Two to three weeks later, the larval cells developed into eight different cell types, which varied in color, form and gene activity. Seven out of the eight continued to divide indefinitely to form new coral cells.

Exploring the symbiosis integral to coral survival

One of the most exciting advancements of this study was that some of the cell lines were similar in form and gene activity to endodermal cells. The endoderm is the inner layer of cells formed about a day after the coral eggs are fertilized.

Importantly, it is the cells in the endoderm that incorporate the symbiotic algae, which photosynthesize and provide nutrients to sustain the coral.

“At this point in time, the most urgent need in coral biology is to understand the interaction between the coral animal and its photosynthetic symbiont at the cellular level, and how this relationship collapses under stress, leading to coral bleaching and death,” said Professor David Miller, a leading coral biologist from James Cook University, Australia, who was not involved in the study.

He continued: “Subject to confirmation that these cells in culture represent coral endoderm, detailed molecular analyses of the coral/photosymbiont interaction would then be possible – and from this, real advances in understanding and perhaps preventing coral bleaching could be expected to flow.”

For Professor Satoh, his interest is in how the photosymbiotic algae cells, which are almost as big as the larval cells, initially enter the coral.

“The algae are incorporated into the coral cells around a week after the larvae first develop,” said Prof. Satoh. “But no one has yet observed this endosymbiotic event on a single-cell level before.”

A new era for coral cell research

The scientists also found that the coral cell lines were still viable after being frozen with liquid nitrogen and then thawed. “This is crucial for being able to successfully supply the coral cell lines to research laboratories across the globe,” said Professor Satoh.

The implications for future research using these cell lines are far-reaching, ranging from research on how single coral cells respond to pollution or higher temperatures, to studying how corals produce the calcium carbonate that builds their skeleton.

Research could also provide further insight into how corals develop, which could improve our ability to farm coral.

In future research, the team hopes to establish cells lines that are clonal, meaning every cell in the culture is genetically identical.

“This will give us a much clearer idea of exactly which coral cell types we are growing, for example gut-like cells or nerve-like cells, by looking at which genes are switched on and off in the cells,” said Professor Satoh.

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Originally Appeared On: https://www.eurekalert.org/pub_releases/2021-04/oios-ses042221.php