17 research outputs found
ΠΡΡΠ°ΡΠΈΠ²Π°Π½ΠΈΠ΅ Ipomoea batatas (L.) Lam. Π² ΡΡΠ»ΠΎΠ²ΠΈΡΡ ΡΠ²Π΅ΡΠΎΠΊΡΠ»ΡΡΡΡΡ in vitro ΠΈ ex vitro
Relevance. Currently, food products that include prebiotics, in particular, inulin, are particularly popular. Interest in this substance is justified by its valuable properties β it is a good immunomodulator, cleanses the body of toxins, radionuclides, "bad" cholesterol, promotes the assimilation of useful trace elements necessary for human life. Inulin is contained in plants such as jerusalem artichoke, chicory, as well as in sweet potatoes, the popularity of which is increasing every year. However, sweet potato plants are afraid of cold and frost-resistant. Therefore, the creation of new varieties and hybrids that are resistant to low temperatures is an urgent problem. Cellular biotechnology is aimed at solving this problem using methods of clonal microreproduction, cell selection, somatic hybridization, etc. For rapid reproduction and obtaining high-quality planting material, biotechnology methods are used, in particular, clonal micro-propagation. However, in this technology there are difficulties associated with poor adaptation of microclones to ex vitro conditions. This fact introduces an additional requirement for the selection of optimal rooting modes in vitro and ex vitro adaptation of microclones.Material and methodology. The aim of the work was to study the influence of cultivation conditions on in vitro rooting and ex vitro adaptation of I. batatas (L.) microclones. The object of the study was sweet potato microgears propagated in vitro. I. batatas micro-gears were cultured in vitro on a Murashige-Skug medium, differing by the type of auxins. The influence of red (R) and far red (FR) light on the shoots rooting in vitro and the adaptation of microclones ex vitro was studied.Results. It has been experimentally established that the cultivation of micro-gears on a medium containing indolyl butyric acid at a concentration of 0.5-1 mg/l and under conditions of illumination by LED lamps of red and far red light in equal amounts leads to the production of microclones with a well-developed root system and vegetative biomass. The use of an aeroponic installation at the last stage of clonal micro-propagation makes it possible to obtain high-quality planting material that can adapt well to open ground conditions.ΠΠΊΡΡΠ°Π»ΡΠ½ΠΎΡΡΡ. Π Π½Π°ΡΡΠΎΡΡΠ΅Π΅ Π²ΡΠ΅ΠΌΡ ΠΎΡΠΎΠ±ΠΎΠΉ ΠΏΠΎΠΏΡΠ»ΡΡΠ½ΠΎΡΡΡΡ ΠΏΠΎΠ»ΡΠ·ΡΡΡΡΡ ΠΏΡΠΎΠ΄ΡΠΊΡΡ ΠΏΠΈΡΠ°Π½ΠΈΡ, Π² ΡΠΎΡΡΠ°Π² ΠΊΠΎΡΠΎΡΡΡ
Π²Ρ
ΠΎΠ΄ΡΡ ΠΏΡΠ΅Π±ΠΈΠΎΡΠΈΠΊΠΈ, Π² ΡΠ°ΡΡΠ½ΠΎΡΡΠΈ, ΠΈΠ½ΡΠ»ΠΈΠ½. ΠΠ½ΡΠ΅ΡΠ΅Ρ ΠΊ Π΄Π°Π½Π½ΠΎΠΌΡ Π²Π΅ΡΠ΅ΡΡΠ²Ρ ΠΎΠΏΡΠ°Π²Π΄Π°Π½ Π΅Π³ΠΎ ΡΠ΅Π½Π½ΡΠΌΠΈ ΡΠ²ΠΎΠΉΡΡΠ²Π°ΠΌΠΈ β ΠΎΠ½ ΡΠ²Π»ΡΠ΅ΡΡΡ Ρ
ΠΎΡΠΎΡΠΈΠΌ ΠΈΠΌΠΌΡΠ½ΠΎΠΌΠΎΠ΄ΡΠ»ΡΡΠΎΡΠΎΠΌ, ΠΎΡΠΈΡΠ°Π΅Ρ ΠΎΡΠ³Π°Π½ΠΈΠ·ΠΌ ΠΎΡ ΡΠΎΠΊΡΠΈΠ½ΠΎΠ², ΡΠ°Π΄ΠΈΠΎΠ½ΡΠΊΠ»ΠΈΠ΄ΠΎΠ², Β«ΠΏΠ»ΠΎΡ
ΠΎΠ³ΠΎΒ» Ρ
ΠΎΠ»Π΅ΡΡΠ΅ΡΠΈΠ½Π°, ΡΠΏΠΎΡΠΎΠ±ΡΡΠ²ΡΠ΅Ρ ΡΡΠ²ΠΎΠ΅Π½ΠΈΡ ΠΏΠΎΠ»Π΅Π·Π½ΡΡ
ΠΌΠΈΠΊΡΠΎΡΠ»Π΅ΠΌΠ΅Π½ΡΠΎΠ², Π½Π΅ΠΎΠ±Ρ
ΠΎΠ΄ΠΈΠΌΡΡ
Π΄Π»Ρ ΠΆΠΈΠ·Π½Π΅Π΄Π΅ΡΡΠ΅Π»ΡΠ½ΠΎΡΡΠΈ ΡΠ΅Π»ΠΎΠ²Π΅ΠΊΠ°. ΠΠ½ΡΠ»ΠΈΠ½ ΡΠΎΠ΄Π΅ΡΠΆΠΈΡΡΡ Π² ΡΠ°ΠΊΠΈΡ
ΡΠ°ΡΡΠ΅Π½ΠΈΡΡ
, ΠΊΠ°ΠΊ ΡΠΎΠΏΠΈΠ½Π°ΠΌΠ±ΡΡ, ΡΠΈΠΊΠΎΡΠΈΠΉ, Π° ΡΠ°ΠΊΠΆΠ΅ Π² Π±Π°ΡΠ°ΡΠ΅, ΠΏΠΎΠΏΡΠ»ΡΡΠ½ΠΎΡΡΡ ΠΊΠΎΡΠΎΡΠΎΠ³ΠΎ Ρ ΠΊΠ°ΠΆΠ΄ΡΠΌ Π³ΠΎΠ΄ΠΎΠΌ Π²ΠΎΠ·ΡΠ°ΡΡΠ°Π΅Ρ. ΠΠ΄Π½Π°ΠΊΠΎ ΡΠ°ΡΡΠ΅Π½ΠΈΡ Π±Π°ΡΠ°ΡΠ° Π±ΠΎΡΡΡΡ Ρ
ΠΎΠ»ΠΎΠ΄Π° ΠΈ Π½Π΅ΠΌΠΎΡΠΎΠ·ΠΎΡΡΡΠΎΠΉΡΠΈΠ²Ρ. ΠΠΎΡΡΠΎΠΌΡ ΡΠΎΠ·Π΄Π°Π½ΠΈΠ΅ Π½ΠΎΠ²ΡΡ
ΡΠΎΡΡΠΎΠ² ΠΈ Π³ΠΈΠ±ΡΠΈΠ΄ΠΎΠ², ΠΎΠ±Π»Π°Π΄Π°ΡΡΠΈΡ
ΡΡΡΠΎΠΉΡΠΈΠ²ΠΎΡΡΡΡ ΠΊ ΠΏΠΎΠ½ΠΈΠΆΠ΅Π½Π½ΡΠΌ ΡΠ΅ΠΌΠΏΠ΅ΡΠ°ΡΡΡΠ°ΠΌ ΡΠ²Π»ΡΠ΅ΡΡΡ Π°ΠΊΡΡΠ°Π»ΡΠ½ΠΎΠΉ ΠΏΡΠΎΠ±Π»Π΅ΠΌΠΎΠΉ. ΠΠ»Π΅ΡΠΎΡΠ½Π°Ρ Π±ΠΈΠΎΡΠ΅Ρ
Π½ΠΎΠ»ΠΎΠ³ΠΈΡ Π½Π°ΠΏΡΠ°Π²Π»Π΅Π½Π° Π½Π° ΡΠ΅ΡΠ΅Π½ΠΈΠ΅ Π΄Π°Π½Π½ΠΎΠΉ ΠΏΡΠΎΠ±Π»Π΅ΠΌΡ Ρ ΠΏΡΠΈΠΌΠ΅Π½Π΅Π½ΠΈΠ΅ΠΌ ΠΌΠ΅ΡΠΎΠ΄ΠΎΠ² ΠΊΠ»ΠΎΠ½Π°Π»ΡΠ½ΠΎΠ³ΠΎ ΠΌΠΈΠΊΡΠΎΡΠ°Π·ΠΌΠ½ΠΎΠΆΠ΅Π½ΠΈΡ, ΠΊΠ»Π΅ΡΠΎΡΠ½ΠΎΠΉ ΡΠ΅Π»Π΅ΠΊΡΠΈΠΈ, ΡΠΎΠΌΠ°ΡΠΈΡΠ΅ΡΠΊΠΎΠΉ Π³ΠΈΠ±ΡΠΈΠ΄ΠΈΠ·Π°ΡΠΈΠΈ ΠΈ Π΄Ρ. ΠΠ»Ρ Π±ΡΡΡΡΠΎΠ³ΠΎ ΡΠ°Π·ΠΌΠ½ΠΎΠΆΠ΅Π½ΠΈΡ ΠΈ ΠΏΠΎΠ»ΡΡΠ΅Π½ΠΈΡ Π²ΡΡΠΎΠΊΠΎΠΊΠ°ΡΠ΅ΡΡΠ²Π΅Π½Π½ΠΎΠ³ΠΎ ΠΏΠΎΡΠ°Π΄ΠΎΡΠ½ΠΎΠ³ΠΎ ΠΌΠ°ΡΠ΅ΡΠΈΠ°Π»Π° ΠΏΡΠΈΠΌΠ΅Π½ΡΡΡ ΠΌΠ΅ΡΠΎΠ΄Ρ Π±ΠΈΠΎΡΠ΅Ρ
Π½ΠΎΠ»ΠΎΠ³ΠΈΠΈ, Π² ΡΠ°ΡΡΠ½ΠΎΡΡΠΈ, ΠΊΠ»ΠΎΠ½Π°Π»ΡΠ½ΠΎΠ΅ ΠΌΠΈΠΊΡΠΎΡΠ°Π·ΠΌΠ½ΠΎΠΆΠ΅Π½ΠΈΠ΅. ΠΠ΄Π½Π°ΠΊΠΎ Π² ΡΡΠΎΠΉ ΡΠ΅Ρ
Π½ΠΎΠ»ΠΎΠ³ΠΈΠΈ ΡΡΡΠ΅ΡΡΠ²ΡΡΡ ΡΡΡΠ΄Π½ΠΎΡΡΠΈ, ΡΠ²ΡΠ·Π°Π½Π½ΡΠ΅ Ρ ΠΏΠ»ΠΎΡ
ΠΎΠΉ Π°Π΄Π°ΠΏΡΠ°ΡΠΈΠ΅ΠΉ ΠΌΠΈΠΊΡΠΎΠΊΠ»ΠΎΠ½ΠΎΠ² ΠΊ ΡΡΠ»ΠΎΠ²ΠΈΡΠΌ ex vitro. ΠΡΠΎΡ ΡΠ°ΠΊΡ Π²Π½ΠΎΡΠΈΡ Π΄ΠΎΠΏΠΎΠ»Π½ΠΈΡΠ΅Π»ΡΠ½ΠΎΠ΅ ΡΡΠ΅Π±ΠΎΠ²Π°Π½ΠΈΠ΅ ΠΊ ΠΏΠΎΠ΄Π±ΠΎΡΡ ΠΎΠΏΡΠΈΠΌΠ°Π»ΡΠ½ΡΡ
ΡΠ΅ΠΆΠΈΠΌΠΎΠ² ΡΠΊΠΎΡΠ΅Π½Π΅Π½ΠΈΡ in vitro ΠΈ Π°Π΄Π°ΠΏΡΠ°ΡΠΈΠΈ ex vitro ΠΌΠΈΠΊΡΠΎΠΊΠ»ΠΎΠ½ΠΎΠ².ΠΠ°ΡΠ΅ΡΠΈΠ°Π» ΠΈ ΠΌΠ΅ΡΠΎΠ΄ΠΈΠΊΠ°. Π¦Π΅Π»ΡΡ ΡΠ°Π±ΠΎΡΡ Π±ΡΠ»ΠΎ ΠΈΠ·ΡΡΠ΅Π½ΠΈΠ΅ Π²Π»ΠΈΡΠ½ΠΈΡ ΡΡΠ»ΠΎΠ²ΠΈΠΉ ΠΊΡΠ»ΡΡΠΈΠ²ΠΈΡΠΎΠ²Π°Π½ΠΈΡ Π½Π° ΡΠΊΠΎΡΠ΅Π½Π΅Π½ΠΈΠ΅ in vitro ΠΈ Π°Π΄Π°ΠΏΡΠ°ΡΠΈΠΈ ex vitro ΠΌΠΈΠΊΡΠΎΠΊΠ»ΠΎΠ½ΠΎΠ² I. batatas (L.). ΠΠ±ΡΠ΅ΠΊΡΠΎΠΌ ΠΈΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½ΠΈΡ Π±ΡΠ»ΠΈ ΠΌΠΈΠΊΡΠΎΡΠ΅ΡΠ΅Π½ΠΊΠΈ Π±Π°ΡΠ°ΡΠ°, ΡΠ°Π·ΠΌΠ½ΠΎΠΆΠ΅Π½Π½ΡΠ΅ in vitro. ΠΠΈΠΊΡΠΎΡΠ΅ΡΠ΅Π½ΠΊΠΈ I. batatas ΠΊΡΠ»ΡΡΠΈΠ²ΠΈΡΠΎΠ²Π°Π»ΠΈ in vitro Π½Π° ΠΏΠΈΡΠ°ΡΠ΅Π»ΡΠ½ΠΎΠΉ ΡΡΠ΅Π΄Π΅, ΡΠΎΠ΄Π΅ΡΠΆΠ°ΡΠ΅ΠΉ ΠΌΠΈΠ½Π΅ΡΠ°Π»ΡΠ½ΡΠ΅ ΡΠΎΠ»ΠΈ ΠΏΠΎ ΠΏΡΠΎΠΏΠΈΡΠΈ ΠΡΡΠ°ΡΠΈΠ³Π° ΠΈ Π‘ΠΊΡΠ³Π°, Π° ΡΠ°ΠΊΠΆΠ΅ ΡΠ°Π·Π»ΠΈΡΠ½ΡΠ΅ Π°ΡΠΊΡΠΈΠ½Ρ. ΠΠ·ΡΡΠ°Π»ΠΈ Π²Π»ΠΈΡΠ½ΠΈΠ΅ ΠΊΡΠ°ΡΠ½ΠΎΠ³ΠΎ (R) ΠΈ Π΄Π°Π»ΡΠ½Π΅Π³ΠΎ ΠΊΡΠ°ΡΠ½ΠΎΠ³ΠΎ (FR) ΡΠ²Π΅ΡΠ° Π½Π° ΡΠΊΠΎΡΠ΅Π½Π΅Π½ΠΈΠ΅ ΠΌΠΈΠΊΡΠΎΠΏΠΎΠ±Π΅Π³ΠΎΠ² in vitro ΠΈ Π°Π΄Π°ΠΏΡΠ°ΡΠΈΡ ΠΌΠΈΠΊΡΠΎΠΊΠ»ΠΎΠ½ΠΎΠ² ex vitro.Π Π΅Π·ΡΠ»ΡΡΠ°ΡΡ. ΠΠΊΡΠΏΠ΅ΡΠΈΠΌΠ΅Π½ΡΠ°Π»ΡΠ½ΠΎ ΡΡΡΠ°Π½ΠΎΠ²Π»Π΅Π½ΠΎ, ΡΡΠΎ Π²ΡΡΠ°ΡΠΈΠ²Π°Π½ΠΈΠ΅ ΠΌΠΈΠΊΡΠΎΡΠ΅ΡΠ΅Π½ΠΊΠΎΠ² Π½Π° ΠΏΠΈΡΠ°ΡΠ΅Π»ΡΠ½ΠΎΠΉ ΡΡΠ΅Π΄Π΅, ΡΠΎΠ΄Π΅ΡΠΆΠ°ΡΠ΅ΠΉ ΠΠΠ Π² ΠΊΠΎΠ½ΡΠ΅Π½ΡΡΠ°ΡΠΈΠΈ 0,5-1 ΠΌΠ³/Π» ΠΈ Π² ΡΡΠ»ΠΎΠ²ΠΈΡΡ
ΠΎΡΠ²Π΅ΡΠ΅Π½ΠΈΡ ΡΠ²Π΅ΡΠΎΠ΄ΠΈΠΎΠ΄Π½ΡΠΌΠΈ Π»Π°ΠΌΠΏΠ°ΠΌΠΈ ΠΊΡΠ°ΡΠ½ΠΎΠ³ΠΎ ΠΈ Π΄Π°Π»ΡΠ½Π΅Π³ΠΎ ΠΊΡΠ°ΡΠ½ΠΎΠ³ΠΎ ΡΠ²Π΅ΡΠ° Π² ΡΠ°Π²Π½ΠΎΠΌ ΡΠΎΠΎΡΠ½ΠΎΡΠ΅Π½ΠΈΠΈ, ΠΏΡΠΈΠ²ΠΎΠ΄ΠΈΡ ΠΊ ΠΏΠΎΠ»ΡΡΠ΅Π½ΠΈΡ ΠΌΠΈΠΊΡΠΎΠΊΠ»ΠΎΠ½ΠΎΠ² Ρ Ρ
ΠΎΡΠΎΡΠΎ ΡΠ°Π·Π²ΠΈΡΠΎΠΉ ΠΊΠΎΡΠ½Π΅Π²ΠΎΠΉ ΡΠΈΡΡΠ΅ΠΌΠΎΠΉ ΠΈ Π½Π°Π΄Π·Π΅ΠΌΠ½ΠΎΠΉ Π±ΠΈΠΎΠΌΠ°ΡΡΠΎΠΉ. ΠΡΠΈΠΌΠ΅Π½Π΅Π½ΠΈΠ΅ Π°ΡΡΠΎΠΏΠΎΠ½Π½ΠΎΠΉ ΡΡΡΠ°Π½ΠΎΠ²ΠΊΠΈ Π½Π° ΠΏΠΎΡΠ»Π΅Π΄Π½Π΅ΠΌ ΡΡΠ°ΠΏΠ΅ ΠΊΠ»ΠΎΠ½Π°Π»ΡΠ½ΠΎΠ³ΠΎ ΠΌΠΈΠΊΡΠΎΡΠ°Π·ΠΌΠ½ΠΎΠΆΠ΅Π½ΠΈΡ ΠΏΠΎΠ·Π²ΠΎΠ»ΡΠ΅Ρ ΠΏΠΎΠ»ΡΡΠ°ΡΡ Π²ΡΡΠΎΠΊΠΎΠΊΠ°ΡΠ΅ΡΡΠ²Π΅Π½Π½ΡΠΉ ΠΏΠΎΡΠ°Π΄ΠΎΡΠ½ΡΠΉ ΠΌΠ°ΡΠ΅ΡΠΈΠ°Π», ΡΠΏΠΎΡΠΎΠ±Π½ΡΠΉ Ρ
ΠΎΡΠΎΡΠΎ ΠΏΠ΅ΡΠ΅Π½ΠΎΡΠΈΡΡ Π°Π΄Π°ΠΏΡΠ°ΡΠΈΡ ΠΊ ΡΡΠ»ΠΎΠ²ΠΈΡΠΌ ΠΎΡΠΊΡΡΡΠΎΠ³ΠΎ Π³ΡΡΠ½ΡΠ°
Monitoring membrane viscosity in differentiating stem cells using BODIPY-based molecular rotors and FLIM
Membrane fluidity plays an important role in many cell functions such as cell adhesion, and migration. In stem cell lines membrane fluidity may play a role in differentiation. Here we report the use of viscosity-sensitive fluorophores based on a BODIPY core, termed βmolecular rotorsβ, in combination with Fluorescence Lifetime Imaging Microscopy, for monitoring of plasma membrane viscosity changes in mesenchymal stem cells (MSCs) during osteogenic and chondrogenic differentiation. In order to correlate the viscosity values with membrane lipid composition, the detailed analysis of the corresponding membrane lipid composition of differentiated cells was performed by time-of-flight secondary ion mass spectrometry. Our results directly demonstrate for the first time that differentiation of MSCs results in distinct membrane viscosities, that reflect the change in lipidome of the cells following differentiation