Multiparametric comparative analysis of coelomocytes in Asterias amurensis and Lysastrosoma anthosticta

Authors

  • Yuriy Karetin A. V. Zhirmunsky Institute of Marine Biology, National Scientific Center of Marine Biology, Far Eastern Branch, Russian Academy of Sciences, Palchevskogo Str, 17, Vladivostok, 690041, Russian Federation https://orcid.org/0000-0002-0760-6721
  • Eugenia Pimenova A. V. Zhirmunsky Institute of Marine Biology, National Scientific Center of Marine Biology, Far Eastern Branch, Russian Academy of Sciences, Palchevskogo Str, 17, Vladivostok, 690041, Russian Federation

DOI:

https://doi.org/10.21638/spbu03.2018.304

Abstract

Behavioral dynamics of coelomocytes from echinoderms Asterias amurensis and Lysastrosoma anthosticta during the first hour of in vitro cultivation was analyzed using a wide range of linear and fractal parameters of the external morphology. Most of the parameters, including values of the cell bounding circle and convex hull, asymmetry, fractal dimensions of contour images, lacunarity, and cell density and area, showed species-specific behavior of the immune cells of the studied animals. The cells differed in a wide range of parameters as early as two min after seeding on the substrate. The cells acquired the largest morphological differences by the fifth min of cultivation. Both cell dynamics in general and analysis of the cell morphology at individual points in time may serve as markers for species-specificity of cells. However, when morphology is compared at one point in time, at least two parameters associated with significant morphological differences in cells of the studied species should be used because of overlapping tendencies in changes in morphological features.

Keywords:

Asterias amurensis, Lysastrosoma anthosticta, coelomocytes, morphometry, fractal analysis, cell morphology

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Published

2018-11-30

How to Cite

Karetin, Y., & Pimenova, E. (2018). Multiparametric comparative analysis of coelomocytes in <em>Asterias amurensis</em> and <em>Lysastrosoma anthosticta</em>. Biological Communications, 63(3), 180–188. https://doi.org/10.21638/spbu03.2018.304

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