Programmed cell death of an identified motoneuron in vitro:: Temporal requirements for steroid exposure and protein synthesis

被引:0
|
作者
Hoffman, KL [1 ]
Weeks, JC [1 ]
机构
[1] Univ Oregon, Inst Neurosci 1254, Eugene, OR 97403 USA
来源
JOURNAL OF NEUROBIOLOGY | 1998年 / 35卷 / 03期
关键词
programmed cell death; steroid hormone; protein synthesis; motoneuron; cell culture; insect;
D O I
10.1002/(SICI)1097-4695(19980605)35:3<300::AID-NEU7>3.0.CO;2-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Ecdysteroid hormones trigger the programmed cell death (PCD) of a segmental subset of accessory planta retractor (APR) motoneurons at pupation in the moth. Manduca sexta. APRs from abdominal segment four [APR(4)s] survive through the pupal stage, whereas homologous APR(6)s die 24-48 h after pupal ecdysis (PE) (the shedding of the larval cuticle), in response to the prepupal peak of ecdysteroids, Following retrograde labeling with the vital fluorescent dye, DiI, the morphology of APR(4)s and APR(6)s in vivo was examined at PE and 24-48 h later. During this period, APR(4) somata remained large and ovoid while APR(6)s somata became shrunken and rounded. Similar phenotypes were observed when DiI-labeled APRs were cultured at PE and examined 24 h to 1 week later. During initial shrinkage and rounding of APR(6)s, the plasma membrane remained intact but DNA condensation occurred and mitochondrial activity was lost. The requirements for ecdysteroids and new protein synthesis for APR(6) death were tested by culturing cells with ecdysteroids and cycloheximide (CHX). When cultured at PE, the death of APR(6)s was independent of further exposure to ecdysteroids and could not be blocked by CHS, In contrast, APR(6)s cultured similar to-24 h earlier required additional exposure to ecdysteroids to die and their death was inhibited by CHS. Thus, the final 24 h of larval life represents an important transition period in the commitment of APR(6)s to undergo PCD, and is of interest for pursuing underlying mechanisms of steroid-induced PCD. (C) 1998 John Wiley & Sons, Inc.
引用
收藏
页码:300 / 322
页数:23
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