Purification and in vitro cultivation of archaeocytes (stem cells) of the marine sponge Hymeniacidon perleve (Demospongiae)
Autor: | Xingju Yu, Wei Zhang, Liming Sun, Yuefan Song, Yi Qu |
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Rok vydání: | 2006 |
Předmět: |
Time Factors
Histology Cell Culture Techniques Artificial seawater Cell Count Cell Separation Biology Pathology and Forensic Medicine Proliferating Cell Nuclear Antigen Botany Animals Mesohyl Telomerase Cell Proliferation Differential centrifugation Stem Cells Cell Biology biology.organism_classification Porifera Cell biology Sponge Bromodeoxyuridine Cell culture Multipotent Stem Cell Stem cell Archaeocyte |
Zdroj: | Cell and Tissue Research. 328:223-237 |
ISSN: | 1432-0878 0302-766X |
DOI: | 10.1007/s00441-006-0342-x |
Popis: | Marine sponges (Porifera) are the best source of marine bioactive metabolites for drug discovery and development, although the sustainable production of most sponge-derived metabolites remains a difficult task. In vitro cultivation of sponge cells in bioreactors has been proposed as a promising technology. However, no continuous cell line has as yet been developed. Archaeocytes are considered to be toti/multipotent stem cells in sponges and, when purified, may allow the development of continuous sponge cell lines. As a prerequisite, we have developed a novel four-step protocol for the purification of archaeocytes from a marine sponge, Hymeniacidon perleve: (1) differential centrifugation to separate large sponge cells including archaeocytes; (2) selective agglomeration in low-Ca(2+)/Mg(2+) artificial seawater in which living archaeocytes form small loose aggregates with some pinacocytes and collencytes; (3) differential adherence to remove anchorage-dependent pinacocytes, collencytes and other mesohyl cells; (4) Ficoll-Vrografin density gradient centrifugation to purify archaeocytes. The final purity of archaeocytes is greater than 80%. The proliferation potential of the archaeocytes has been demonstrated by high levels of BrdU incorporation, PCNA expression and telomerase activity. In 4-day primary cultures, the purified archaeocytes show a 2.5-fold increase in total cell number. This study opens an important avenue towards developing sponge cell cultures for the commercial exploitation of sponge-derived drugs. |
Databáze: | OpenAIRE |
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