ESTABLISHMENT OF PHAGOCYTIC CELL LINES FROM LARVAL HEMOCYTES OF THE BEET ARMYWORM, SPODOPTERA EXIGUA

Hemolymph was taken from beet armyworm (Spodoptera exigua) larvae and a new hemocyte cell line (SeHe920-1a) was established by supplementing the culture medium with a reduced form of glutathione to avoid the activation of prophenoloxidase cascade. To evaluate the phagocytic ability of the SeHe920-1a...

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Published inIn vitro cellular & developmental biology. Animal Vol. 40; no. 7; pp. 183 - 186
Main Authors CHISA, YASUNAGA-AOKI, IMANISHI, SHIGEO, IIYAMA, KAZUHIRO, KAWARABATA, TAKESHI
Format Journal Article
LanguageEnglish
Published Germany Society for In Vitro Biology 01.07.2004
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ISSN1071-2690
1543-706X
1543-706X
DOI10.1290/1543-706X(2004)40<183:EOPCLF>2.0.CO;2

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Summary:Hemolymph was taken from beet armyworm (Spodoptera exigua) larvae and a new hemocyte cell line (SeHe920-1a) was established by supplementing the culture medium with a reduced form of glutathione to avoid the activation of prophenoloxidase cascade. To evaluate the phagocytic ability of the SeHe920-1a cells, polystyrene microspheres of two sizes (6.14 ± 0.45 μm and 2.84 ± 0.14 μm in diameter) and inactivated spores of an entomopathogenic microsporidium, Vairimorpha sp. NIS M12 (5.10 ± 0.21 μm × 2.00 ± 0.11 μm), were introduced into the cell culture. The SeHe920-1a cells had higher phagocytic ability than other lepidopteran cell lines that were not derived from the hemocytes. When microsporidian spores were inoculated, 27% of SeHe920-1a cells were observed to take up spores (average 1.7 spores per cell). By cloning SeHe920-1a cells, 12 cell lines were established and designated SeHe920Y1 to SeHe920Y12. In comparison with the parental cell line, phagocytic activity was enhanced in SeHe920Y6, SeHe920Y10, and SeHe920Y11 cell lines and especially in the SeHe920Y7 cell line, where approximately 50% of cells were phagocytic and the average number of microsporidian spores engulfed per cell was twice that of the SeHe920-1a cell line.
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ISSN:1071-2690
1543-706X
1543-706X
DOI:10.1290/1543-706X(2004)40<183:EOPCLF>2.0.CO;2