Increased cell proliferation and mucocyte density in the sea anemone Aiptasia pallida recovering from bleaching

PLoS One. 2013 May 28;8(5):e65015. doi: 10.1371/journal.pone.0065015. Print 2013.

Abstract

Recovery of coral after bleaching episodes is a critical period for the health of the reef ecosystem. While events such as symbiont (genus Symbiodinium) shifting/shuffling or tissue apoptosis have been demonstrated to occur following bleaching, little is known concerning tissue recovery or cell proliferation. Here, we studied the sea anemone Aiptasia pallida exposed to a transient elevation of water temperature combined with high illumination (33°C and 1900 µmol photons x m(-2) x s(-1) for 30 h). Following such treatment bleached anemones showed a significant reduction of their Symbiodinium density. Cell proliferation in the ectodermis and gastrodermis was determined by assessing the densities of cells labeled with a thymidine analogue (EdU). Cell proliferation significantly increased during the first day following stress in both tissue types. This increased cell proliferation returned to pre-stress values after one week. Although cell proliferation was higher in the ectodermis in absence of stress, it was relatively more pronounced in the gastrodermis of stressed anemones. In addition, the ratio of ectodermal mucocytes significantly increased three weeks after induced stress. These results suggest that thermal/photic stress coupled with the loss of the symbionts is able to enhance cell proliferation in both gastrodermis and ectodermis of cnidarians. While new cells formed in the gastrodermis are likely to host new Symbiodinium, the fate of new cells in the ectodermis was only partially revealed. Some new ectodermal cells may, in part, contribute to the increased number of mucocytes which could eventually help strengthen the heterotrophic state until restoration of the symbiosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Count
  • Cell Proliferation
  • Dinoflagellida / physiology
  • Organ Specificity
  • Population Dynamics
  • Sea Anemones / cytology*
  • Sea Anemones / physiology*
  • Stress, Physiological*
  • Temperature
  • Wheat Germ Agglutinins / metabolism

Substances

  • Wheat Germ Agglutinins

Grants and funding

DF is a recipient of a F.R.I.A PhD Studentship, SR is a research fellow of the F.R.S-F.N.R.S. LT and OHG were supported by funding from the Great Barrier Reef Foundation, the Queensland Smart State Fellowship Award (to OHG) and the ARC Centre of Excellence for Coral Reef Studies. JCP was supported by funding from the F.R.S.-F.N.R.S. (FRFC 2.4.631.09) and from the University of Liège. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.