Limitations in the isolation and stimulation of splenic mononuclear cells in a dasyurid marsupial, Phascogale calura

• Published in: BMC research notes 2018-10, Vol.11 (1), p.712-712, Article 712
• Main Authors: Letendre, C, Young, L J, Old, J M
• Format: Article
• Language: English
• Subjects: Animal behavior; Animals; Australia; Cell culture; Cell proliferation; Cell Separation - methods; Centrifugation; Colorimetry; Cytokines; Dasyurid; Female; Flow cytometry; Immune system; Immunology; Leukocytes (mononuclear); Leukocytes, Mononuclear - cytology; Leukocytes, Mononuclear - drug effects; Leukocytes, Mononuclear - immunology; Lymphocytes; Male; Mammals; Marsupialia - immunology; Marsupials; Mononuclear cells; PBMC; Peripheral blood mononuclear cells; Phascogale calura; Phytohemagglutinins - pharmacology; Primary Cell Culture; Research Note; Spleen; Spleen - cytology; Spleen - drug effects; Spleen - immunology; T cell receptors; Tumor necrosis factor-TNF
• ISSN: 1756-0500; 1756-0500
• DOI: 10.1186/s13104-018-3824-5

Marsupials suffer from an increasing number of stressors in this changing world. Functional studies are thus needed to broaden our understanding of the marsupial immune system. The red-tailed phascogale (Phascogale calura) is a small Australian marsupial previously used in descriptive immunological studies. Here, we aimed to develop functional assays by isolating and stimulating blood and spleen mononuclear cells in vitro. While peripheral blood mononuclear cell (PBMC) were relatively easy to isolate, only 10 mononuclear cells (> 90% purity and > 75% viability) could be recovered from the spleen, independently of the sex and age of the animal or the centrifugation time and speed tested. The pores of the mesh sieve used for tissue homogenization might have been too big to yield a single cell suspension. Nevertheless, in spite of the overall low number of cells recovered, PBMC and splenic mononuclear cells were successfully activated in preliminary trials with phytohemaglutinin. This activation state was evidenced by a change in shape and the presence of small cell aggregations in the mitogen-stimulated cultures. A non-radioactive colorimetric assay was also performed to confirm cell proliferation in these wells. This work highlights the importance of developing and reporting detailed methodological protocols in non-traditional research species.