Cryopreservation effect on proliferation and differentiation potential of cultured chorion cells
NA Volkova, AN Goltsev - CryoLetters, 2015 - ingentaconnect.com
CryoLetters, 2015•ingentaconnect.com
BACKGROUND: Fetoplacental tissues including the early chorion contain stem cells with
various morphological and functional characteristics. Cultured chorionic cells may be used
in perspective therapies of different pathologies. OBJECTIVE: To investigate the effect of
cryopreservation on proliferation and differentiation potential of chorion cell culture (ChCC).
MATERIALS AND METHODS: Five freezing programs for ChCC were compared: Program 1,
cooling from 25° C down to-30° C at 0.5° C/min; Program 2, cooling from 25° C down to-30° …
various morphological and functional characteristics. Cultured chorionic cells may be used
in perspective therapies of different pathologies. OBJECTIVE: To investigate the effect of
cryopreservation on proliferation and differentiation potential of chorion cell culture (ChCC).
MATERIALS AND METHODS: Five freezing programs for ChCC were compared: Program 1,
cooling from 25° C down to-30° C at 0.5° C/min; Program 2, cooling from 25° C down to-30° …
BACKGROUND
Fetoplacental tissues including the early chorion contain stem cells with various morphological and functional characteristics .Cultured chorionic cells may be used in perspective therapies of different pathologies.
OBJECTIVE
To investigate the effect of cryopreservation on proliferation and differentiation potential of chorion cell culture (ChCC).
MATERIALS AND METHODS
Five freezing programs for ChCC were compared: Program 1, cooling from 25°C down to -30°C at 0.5°C/min; Program 2, cooling from 25°C down to -30°C at 1°C/min; Program 3, cooling from 25°C down to -10°C at 1°C/min with further cooling down to - 80°C at 10°C/min; Program 4, cooling from 25°C down to -5°C at 1°C/min with further cooling down to -80°C at 10°C/min; Program 5, cooling from 25°C down to -6°C at 1°C/min with further crystal seeding by adding the surplus nitrogen into the chamber, and cooling down to -80°C at 10°C/min. Viability, adhesion, proliferation and directed differentiation were examined.
RESULTS
Freezing program 5 achieved the best result, with the highest viability, adhesion, proliferation and directed differentiation.
CONCLUSION
The data may help establishing better cryopreservation protocols for perspective chorionic cell lines and their further application in biotechnology.
ingentaconnect.com
以上显示的是最相近的搜索结果。 查看全部搜索结果