Distribution patterns and morphology of sensilla on the antennae of Plutella xylostella (L.)-A scanning and transmission electron microscopic study.

The antennal morphology, types of antennal sensilla, fine structures and distributions of the sensilla in Plutella xylostella L. (Lepidoptera: Plutellidae) were studied by scanning (SEM) and transmission (TEM) electron microscopy. The antenna, scape, pedicel and flagellum were all longer in males than in females. A total of seventeen types of sensilla were identified on the antennae: trichodea (two subtypes), basiconica, coeloconica (three subtypes), Böhm's bristles (two subtypes), styloconica (two subtypes), squamiformia, auricillica, furcatea (three subtypes), cupuliform organs and terminal sensory pegs. Their numbers and distributions were studied in both male and female, and we found some of the sensilla exhibited various degrees of sexual dimorphisms. Sensilla trichodea were the most abundant of all sensillum types whereas terminal peg was present only once per antenna. Sensilla trichodea in males were bigger (subtype I) and more abundant than in females, however, sensilla basiconica and squamiformia were significantly smaller and less abundant in males than in females. Sensilla styloconica II was only found in females. Seven common sensillum types were studied with TEM to reveal its fine internal structure providing morphological evidences of their sensory functions. Sensilla trichodea I, basiconica and coeloconica III have porous walls suggesting olfactory functions. Combined with the sexual dimorphism, sensilla trichodea male P. xylostella might be involved in detecting sexual pheromones and sensilla basiconica of female might respond to host plant volatiles. Whereas sensilla coeloconica (subtype I and II) and Böhm's bristles have nonporous walls suggesting non-olfactory functions. The study presented a thorough inventory of sensilla on the antennae and laid a solid foundation for future functional studies of these sensilla in this important economical pest.

[Identification of differentially expressed genes of acute hypoxia-treated HepG2 cells and hypoxia-acclimatized HepG2 cells].

To provide necessary information for further understanding of molecular mechanism of hypoxia acclimatization, the differentially expressed genes of HepG2 cells exposed to normoxia, acute hypoxia-treated cells which were exposed to 1% oxygen for 48 h, and hypoxia-acclimatized HepG2 cells which were cultured for 6 circles of alternate low oxygen (1% oxygen for 24 h) and normal oxygen (21% oxygen for 24 h), were identified respectively by combining the suppression subtractive hybridization (SSH) and cDNA microarray. Thirty-seven genes were expressed differentially in cells exposed to 1% oxygen for 48 h compared with those in cells exposed to normoxia. The expression of all these 37 genes was down-regulated, including the genes participating in cell cycle, cell response to stimulus, and cell signal transduction, and cell cytoskeleton formation, the genes associated with transcription and cell metabolism, 4 expressed sequence tags (ESTs), and 12 genes of which the functions are not known. There is a novel gene sequence, which has not been found in existing databases. There were only 6 genes differentially expressed in the hypoxia-acclimatized cells compared with cells exposed to normoxia, including two mitochondrion genes, metalloprotease-1 gene, ferritin gene, thymosin beta-4 and TPT1 genes. The expressions of mitochondrion ND4, ferritin, thymosin beta-4 and TPT1 were up-regulated, while the expressions of mitochondrion ND1 gene and metalloproease-1 gene were down-regulated. Cell tolerance to hypoxia increased after the cells were hypoxia-acclimatized. The different gene expression patterns of the acute hypoxia-treated cells and the hypoxia-acclimatized cells may be related to the increased tolerance of the cells to hypoxia.