scholarly journals 20E-dependent regulation of growth and secondary metabolism of cell culture Lychnis chalcedonica L.

2019 ◽  
Author(s):  
I.F. Golovatskaya ◽  
◽  
M.V. Nechaeva ◽  
E.V. Boiko ◽  
◽  
...  
Keyword(s):  
Cell Culture ◽  
Secondary Metabolism ◽  
Regulation Of Growth

Kinetin regulation of growth and secondary metabolism in waterlogging and salinity treated Vigna sinensis and Zea mays

2002 ◽  
Vol 24 (1) ◽  
pp. 19-27 ◽  
Author(s):  
Mamdouh M. Nemat Alla ◽  
Mahmoud E. Younis ◽  
Omar A. El-Shihaby ◽  
Zeinab M. El-Bastawisy
Keyword(s):  
Zea Mays ◽  
Secondary Metabolism ◽  
Vigna Sinensis ◽  
Regulation Of Growth

scholarly journals The effect of sodium selenite on the secondary metabolism of cell culture Lychnis chalcedonica in vitro

2020 ◽  
Author(s):  
M. V. Nechaeva ◽  
I. F. Golovatskaya
Keyword(s):  
Cell Culture ◽  
Secondary Metabolism ◽  
Sodium Selenite ◽  
Flavonoid Content ◽  
Culture In Vitro ◽  
L Cell ◽  
Low Concentrations

We studied the effect of sodium selenite (Se) on the secondary metabolism of Lychnis chalcedonica L. cell culture in vitro. It was found that low concentrations of Se reduce the flavonoid content, but do not change the content of saponins.

A T.E.M. study of mouse mammary epithelial cell secretory differentiation cultured on collagen and Matrigel

1991 ◽  
Vol 49 ◽  
pp. 188-189
Author(s):  
W.N. Bentham ◽  
V. Rocha
Keyword(s):  
Cell Culture ◽  
Mammary Epithelial ◽  
Secretory Process ◽  
Cell Culture System ◽  
Protein Maturation ◽  
Cell Culture Techniques ◽  
Culture Techniques ◽  
Mouse Mammary Epithelial Cell ◽  
Secretory Differentiation

It has been an interest of our lab to develop a mammary epethelial cell culture system that faithfully duplicates the in vivo condition of the lactating gland. Since the introduction of collagen as a matrix on which cells are cultivated other E.C.M. type matrices have been made available and are used in many cell culture techniques. We have previously demonstrated that cells cultured on collagen and Matrigel do not differentiate as they do in vivo. It seems that these cultures often produce cells that show a disruption in the secretory process. The appearance of large ribosomal studded vesicles, that specifically label with antibody to casein, suggest an interruption of both protein maturation and secretion at the E.R. to golgi transition. In this report we have examined cultures on collagen and Matrigel at relative high and low seeding densities and compared them to cells from the in vivo condition.

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