Morphogenesis in Insect Tissue Culture

1982 ◽  
pp. 237-265 ◽  
Author(s):  
Herbert Oberlander ◽  
Dwight E. Lynn
Science ◽  
1964 ◽  
Vol 144 (3625) ◽  
pp. 1465-1467 ◽  
Author(s):  
H. Hirumi ◽  
K. Maramorosch

Nature ◽  
1960 ◽  
Vol 187 (4743) ◽  
pp. 1072-1074 ◽  
Author(s):  
B. M. JONES ◽  
I. CUNNINGHAM

2004 ◽  
Vol 72 (6) ◽  
pp. 3693-3694 ◽  
Author(s):  
T. Harry Birkbeck ◽  
Angela A. Griffen ◽  
Helen I. Reid ◽  
L. Anthony Laidler ◽  
Simon Wadsworth

ABSTRACT Piscirickettsia salmonis was grown in established insect, frog, and fish tissue culture cells. The yield of P. salmonis in Sf21 cells was up to 100 times that obtained in CHSE-214 cells, and virulence for Atlantic salmon was retained. The ceiling temperature for growth of P. salmonis in Sf21 cells was 24°C.


1971 ◽  
Vol 49 (10) ◽  
pp. 1355-1358 ◽  
Author(s):  
S. S. Sohi

Prolonged culturing of the hemocytes of Malacosoma disstria has been accomplished using Grace's insect tissue culture medium supplemented with fetal bovine serum (5%) and Bombyx mori hemolymph (3%). The cultures started to grow after 3–6 months. These cells have now been in vitro for over 16 months, and have been subcultured 35 times. Three types of cells were present in primary cultures, but only one type, prohemocytes, persisted and grew after subculturing. The M. disstria larvae that were used as the original source of hemocytes were naturally infected with the microsporidian Glugea disstriae. The microsporidian also grew in [he cell cultures, and the cells are still infected.


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