Кріоконсервування мультиклітинних сфероїдів, отриманих із первинної культури клітин спінальних гангліїв новонароджених поросят

Dorsal root ganglia (DRG) are a potential source of neural stem cells, since they contain the neural crest-derived cells capable to differentiate into neurons and different subpopulations of glial cells. It is known that under certain culture conditions, the DRG cells, derived from neonatal piglet...

Повний опис

Збережено в:
Бібліографічні деталі
Дата:2019
Автори: Ali, Sabina G., Bozhok, Galina A.
Формат: Стаття
Мова:English
Опубліковано: Publishing House ‘Akademperiodyka’ of the National Academy of Sciences of Ukraine; Institute for Problems of Cryobiology and Cryomedicine 2019
Теми:
Онлайн доступ:https://cryo.org.ua/journal/index.php/probl-cryobiol-cryomed/article/view/1563
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Назва журналу:Problems of Cryobiology and Cryomedicine

Репозитарії

Problems of Cryobiology and Cryomedicine
Опис
Резюме:Dorsal root ganglia (DRG) are a potential source of neural stem cells, since they contain the neural crest-derived cells capable to differentiate into neurons and different subpopulations of glial cells. It is known that under certain culture conditions, the DRG cells, derived from neonatal piglets form the floating multicellular spheroids (MSs), capable to produce the fibroblast-like cells (FLCs), glial cells (GCs) and neuron-like cells (NLCs). Here, we have cryopreserved the MSc, derived under serum-free culture conditions using 5, 7.5, 10% dimethyl sulfoxide (DMSO) and two-stage regimen of freezing. After cryopreservation, the MSs were established to preserve the capability to adhere as well as to produce three cell types: FLCs, GCs and NLCs. However, the capability of frozen-thawed MSs to produce different cell types was reduced. The cryoprotectant concentration affected the cell type, prevailing in the culture, derived from the frozen-thawed MSs. After cryopresevation with 10% DMSO, the monolayer consisted mainly of FLCs, while with 5 and 7.5% DMSO it mostly comprised GLCs. Probl Cryobiol Cryomed 2019; 29(4): 354-364