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Coral cell separation and isolation by fluorescence-activated cell sorting (FACS).
Rosental, Benyamin; Kozhekbaeva, Zhanna; Fernhoff, Nathaniel; Tsai, Jonathan M; Traylor-Knowles, Nikki.
Afiliação
  • Rosental B; Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA. benyamin@stanford.edu.
  • Kozhekbaeva Z; Department of Pathology, Hopkins Marine Station, Stanford University, 120 Ocean View Blvd, Pacific Grove, CA, 93950, USA. benyamin@stanford.edu.
  • Fernhoff N; University of Miami, Rosenstiel School of Marine and Atmospheric Science, 4600 Rickenbacker Causeway, Florida, 33149, USA.
  • Tsai JM; Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA.
  • Traylor-Knowles N; Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA.
BMC Cell Biol ; 18(1): 30, 2017 08 29.
Article em En | MEDLINE | ID: mdl-28851289
ABSTRACT

BACKGROUND:

Generalized methods for understanding the cell biology of non-model species are quite rare, yet very much needed. In order to address this issue, we have modified a technique traditionally used in the biomedical field for ecological and evolutionary research. Fluorescent activated cell sorting (FACS) is often used for sorting and identifying cell populations. In this study, we developed a method to identify and isolate different cell populations in corals and other cnidarians.

METHODS:

Using fluorescence-activated cell sorting (FACS), coral cell suspension were sorted into different cellular populations using fluorescent cell markers that are non-species specific. Over 30 different cell markers were tested. Additionally, cell suspension from Aiptasia pallida was also tested, and a phagocytosis test was done as a downstream functional assay.

RESULTS:

We found that 24 of the screened markers positively labeled coral cells and 16 differentiated cell sub-populations. We identified 12 different cellular sub-populations using three markers, and found that each sub-population is primarily homogeneous. Lastly, we verified this technique in a sea anemone, Aiptasia pallida, and found that with minor modifications, a similar gating strategy can be successfully applied. Additionally, within A. pallida, we show elevated phagocytosis of sorted cells based on an immune associated marker.

CONCLUSIONS:

In this study, we successfully adapted FACS for isolating coral cell populations and conclude that this technique is translatable for future use in other species. This technique has the potential to be used for different types of studies on the cellular stress response and other immunological studies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Biomarcadores / Separação Celular / Antozoários / Citometria de Fluxo Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: BMC Cell Biol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Biomarcadores / Separação Celular / Antozoários / Citometria de Fluxo Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: BMC Cell Biol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos