Форма представления | Статьи в российских журналах и сборниках |
Год публикации | 2022 |
Язык | английский |
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Аймалетдинов Александр Маазович, автор
Закирова Елена Юрьевна, автор
Ризванов Альберт Анатольевич, автор
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Rutland Catrin , автор
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Курилов Игорь Витальевич, автор
Юферова Алина Константиновна, автор
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Библиографическое описание на языке оригинала |
Aimaletdinov A. М. Isolation, culturing and 3D bioprinting equine myoblasts / А.М.Aimaletdinov, М. Abyzova, I. Kurilov, A. Yuferova, C. Rutland, A.A. Rizvanov, E.Yu. Zakirova // Biological Communications. - 2022. - № 67(3). - р.152–159. |
Аннотация |
Isolating and culturing myoblasts is essential for techniques such as tissue regeneration and in vitro meat production. This research describes a protocol to isolate primary myoblasts from skeletal muscle of an adult horse. The equine primary myoblasts expressed markers specific to myoblasts and had multipotent potential capabilities with differentiation into chondrocytes, adipocytes and osteoblasts in vitro. The horse myoblasts did not adhere to Cytodex 3 and grew poorly on CultiSpher-S microcarriers during in vitro cultivation. Our studies showed that the use of GelMa bioink and ionic cross-linking did not have negative effects on cell proliferation at the beginning of cultivation. However, cells showed reduced proliferative activity by day 40 following in vitro culturing. The population of primary equine myoblasts obtained from an adult individual, and propagated on microcarriers and bioink, did not meet the requirements of the regenerative veterinary and manufacturing meat in vitro regarding the quantity and quality of the cells required. Nonetheless, further optimization of the cell scaling up process, including both microcarriers and/or the bioreactor program and bioprinting, is still important. |
Ключевые слова |
myoblasts, bioprinting, microcarriers |
Название журнала |
Biological Communications
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URL |
https://doi.org/10.21638/spbu03.2022.302 |
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https://repository.kpfu.ru/?p_id=272340 |
Файлы ресурса | |
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Полная запись метаданных |
Поле DC |
Значение |
Язык |
dc.contributor.author |
Аймалетдинов Александр Маазович |
ru_RU |
dc.contributor.author |
Закирова Елена Юрьевна |
ru_RU |
dc.contributor.author |
Ризванов Альберт Анатольевич |
ru_RU |
dc.contributor.author |
Rutland Catrin |
ru_RU |
dc.contributor.author |
Курилов Игорь Витальевич |
ru_RU |
dc.contributor.author |
Юферова Алина Константиновна |
ru_RU |
dc.date.accessioned |
2022-01-01T00:00:00Z |
ru_RU |
dc.date.available |
2022-01-01T00:00:00Z |
ru_RU |
dc.date.issued |
2022 |
ru_RU |
dc.identifier.citation |
Aimaletdinov A. М. Isolation, culturing and 3D bioprinting equine myoblasts / А.М.Aimaletdinov, М. Abyzova, I. Kurilov, A. Yuferova, C. Rutland, A.A. Rizvanov, E.Yu. Zakirova // Biological Communications. - 2022. - № 67(3). - р.152–159. |
ru_RU |
dc.identifier.uri |
https://repository.kpfu.ru/?p_id=272340 |
ru_RU |
dc.description.abstract |
Biological Communications |
ru_RU |
dc.description.abstract |
Isolating and culturing myoblasts is essential for techniques such as tissue regeneration and in vitro meat production. This research describes a protocol to isolate primary myoblasts from skeletal muscle of an adult horse. The equine primary myoblasts expressed markers specific to myoblasts and had multipotent potential capabilities with differentiation into chondrocytes, adipocytes and osteoblasts in vitro. The horse myoblasts did not adhere to Cytodex 3 and grew poorly on CultiSpher-S microcarriers during in vitro cultivation. Our studies showed that the use of GelMa bioink and ionic cross-linking did not have negative effects on cell proliferation at the beginning of cultivation. However, cells showed reduced proliferative activity by day 40 following in vitro culturing. The population of primary equine myoblasts obtained from an adult individual, and propagated on microcarriers and bioink, did not meet the requirements of the regenerative veterinary and manufacturing meat in vitro regarding the quantity and quality of the cells required. Nonetheless, further optimization of the cell scaling up process, including both microcarriers and/or the bioreactor program and bioprinting, is still important. |
ru_RU |
dc.language.iso |
ru |
ru_RU |
dc.subject |
myoblasts |
ru_RU |
dc.subject |
bioprinting |
ru_RU |
dc.subject |
microcarriers |
ru_RU |
dc.title |
Isolation, culturing and 3D bioprinting equine myoblasts |
ru_RU |
dc.type |
Статьи в российских журналах и сборниках |
ru_RU |
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