Inhibitory effects of starvation on prothoracic gland cell DNA synthesis during the last larval instar of the silkworm, Bombyx mori

被引:3
作者
Chen, Chien-Hung [2 ]
Gu, Shi-Hong [1 ]
机构
[1] Natl Museum Nat Sci, Dept Zool, Taichung 40419, Taiwan
[2] Chung Hwa Univ Med Technol, Tainan, Taiwan
来源
JOURNAL OF EXPERIMENTAL ZOOLOGY PART A-ECOLOGICAL GENETICS AND PHYSIOLOGY | 2008年 / 309A卷 / 07期
关键词
D O I
10.1002/jez.463
中图分类号
Q95 [动物学];
学科分类号
071002 ;
摘要
Activation of DNA synthesis in prothoracic gland cells of the silkworm, Bombyx mori, during the middle stages of the last larval instar appears to be nutrition dependent, with starvation on day 3 of the last larval instar inhibiting its dramatic increase. The possible cellular mechanism causing the inhibition of DNA synthesis owing to starvation was further examined by determining changes in the growth-promoting activity of the hemolymph and the responsiveness of gland cells to starvation. The results showed that on starvation, the activity of the growth-promoting factor in the hemolymph did not greatly decrease until 2 days after starvation had begun. However, the dramatic increase in the responsiveness of gland cells (the ability to synthesize DNA when exposed to the hemolymph growth factor), which normally occurs on day 4 of the last instar, was not observed when starvation was begun on day 3. A dramatic increase in gland cell size was observed in control larvae during later stages of the last larval instar. However, with starvation beginning on day 3, gland cell size was maintained at lower levels compared with those of control larvae, indicating that the inhibition of DNA synthesis is indeed related to the inhibition of cell size. From these results, it was assumed that alterations in growth factor receptors and downstream signaling may be related to the inhibition of DNA synthesis by starvation and that the deficiency in growth-promoting factor signaling may guarantee that the growth of endoreplicative tissues in these larvae ceases.
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页码:399 / 406
页数:8
相关论文
共 34 条
[1]  
Britton JS, 1998, DEVELOPMENT, V125, P2149
[2]   Drosophila's insulin/P13-kinase pathway coordinates cellular metabolism with nutritional conditions [J].
Britton, JS ;
Lockwood, WK ;
Li, L ;
Cohen, SM ;
Edgar, BA .
DEVELOPMENTAL CELL, 2002, 2 (02) :239-249
[3]   An evolutionarily conserved function of the Drosophila insulin receptor and insulin-like peptides in growth control [J].
Brogiolo, W ;
Stocker, H ;
Ikeya, T ;
Rintelen, F ;
Fernandez, R ;
Hafen, E .
CURRENT BIOLOGY, 2001, 11 (04) :213-221
[4]   Ras activity in the Drosophila prothoracic gland regulates body size and developmental rate via ecdysone release [J].
Caldwell, PE ;
Walkiewicz, M ;
Stern, M .
CURRENT BIOLOGY, 2005, 15 (20) :1785-1795
[5]   Stage-dependent effects of starvation on the growth, metamorphosis, and ecdysteroidogenesis by the prothoracic glands during the last larval instar of the silkworm, Bombyx mori [J].
Chen, Chien-Hung ;
Gu, Shi-Hong .
JOURNAL OF INSECT PHYSIOLOGY, 2006, 52 (09) :968-974
[6]   MORPHOMETRIC ANALYSIS OF CORPUS ALLATUM CELLS IN ADULT FEMALES OF 3 COCKROACH SPECIES [J].
CHIANG, AS ;
GADOT, M ;
SCHAL, C .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1989, 67 (2-3) :179-184
[7]   Antagonistic actions of ecdysone and insulins determine final size in Drosophila [J].
Colombani, J ;
Bianchini, L ;
Layalle, S ;
Pondeville, E ;
Dauphin-Villemant, C ;
Antoniewski, C ;
Carré, C ;
Noselli, S ;
Léopold, P .
SCIENCE, 2005, 310 (5748) :667-670
[8]   Size control in animal development [J].
Conlon, I ;
Raff, M .
CELL, 1999, 96 (02) :235-244
[9]  
Day SJ, 2000, DEVELOPMENT, V127, P2977
[10]  
DORN A, 1976, CELL TISSUE RES, V171, P331