Multidendritic sensory neurons in the adult Drosophila abdomen: origins, dendritic morphology, and segment- and age-dependent programmed cell death

被引:72
作者
Shimono, Kohei [2 ]
Fujimoto, Azusa [2 ]
Tsuyama, Taiichi [2 ]
Yamamoto-Kochi, Misato [2 ]
Sato, Motohiko [2 ,3 ]
Hattori, Yukako [2 ]
Sugimura, Kaoru [2 ,4 ]
Usui, Tadao [2 ]
Kimura, Ken-ichi [1 ]
Uemura, Tadashi [2 ]
机构
[1] Hokkaido Univ, Sapporo, Hokkaido 0028502, Japan
[2] Kyoto Univ, Lab Cell Recognit & Pattern Format, Grad Sch Biostudies, Sakyo Ku, Kyoto 6068507, Japan
[3] Kyoto Univ, Lab Neural Dev, Grad Sch Biostudies, Kyoto 6068501, Japan
[4] RIKEN, Lab Cell Funct Dynam, Adv Technol Dev Grp, Brain Sci Inst, Wako, Saitama 3510198, Japan
来源
NEURAL DEVELOPMENT | 2009年 / 4卷
关键词
FINGER PROTEIN ABRUPT; VIVO TIME-LAPSE; IN-VIVO; INSECT METAMORPHOSIS; CAFFEINE RESPONSE; NERVOUS-SYSTEM; MELANOGASTER; MECHANISMS; EXPRESSION; MORPHOGENESIS;
D O I
10.1186/1749-8104-4-37
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: For the establishment of functional neural circuits that support a wide range of animal behaviors, initial circuits formed in early development have to be reorganized. One way to achieve this is local remodeling of the circuitry hardwiring. To genetically investigate the underlying mechanisms of this remodeling, one model system employs a major group of Drosophila multidendritic sensory neurons - the dendritic arborization (da) neurons - which exhibit dramatic dendritic pruning and subsequent growth during metamorphosis. The 15 da neurons are identified in each larval abdominal hemisegment and are classified into four categories - classes I to IV - in order of increasing size of their receptive fields and/or arbor complexity at the mature larval stage. Our knowledge regarding the anatomy and developmental basis of adult da neurons is still fragmentary. Results: We identified multidendritic neurons in the adult Drosophila abdomen, visualized the dendritic arbors of the individual neurons, and traced the origins of those cells back to the larval stage. There were six da neurons in abdominal hemisegment 3 or 4 (A3/4) of the pharate adult and the adult just after eclosion, five of which were persistent larval da neurons. We quantitatively analyzed dendritic arbors of three of the six adult neurons and examined expression in the pharate adult of key transcription factors that result in the larval class-selective dendritic morphologies. The 'baseline design' of A3/4 in the adult was further modified in a segment-dependent and age-dependent manner. One of our notable findings is that a larval class I neuron, ddaE, completed dendritic remodeling in A2 to A4 and then underwent caspase-dependent cell death within 1 week after eclosion, while homologous neurons in A5 and in more posterior segments degenerated at pupal stages. Another finding is that the dendritic arbor of a class IV neuron, v'ada, was immediately reshaped during post-eclosion growth. It exhibited prominent radial-to-lattice transformation in 1-day-old adults, and the resultant lattice-shaped arbor persisted throughout adult life. Conclusion: Our study provides the basis on which we can investigate the genetic programs controlling dendritic remodeling and programmed cell death of adult neurons, and the life-long maintenance of dendritic arbors.
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页数:21
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