RT Journal Article
SR Electronic
T1 Temperature-Dependent Developmental Plasticity of <em>Drosophila</em> Neurons: Cell-Autonomous Roles of Membrane Excitability, Ca<sup>2+</sup> Influx, and cAMP Signaling
JF The Journal of Neuroscience
JO J. Neurosci.
FD Society for Neuroscience
SP 12611
OP 12622
DO 10.1523/JNEUROSCI.2179-07.2007
VO 27
IS 46
A1 I-Feng Peng
A1 Brett A. Berke
A1 Yue Zhu
A1 Wei-Hua Lee
A1 Wenjia Chen
A1 Chun-Fang Wu
YR 2007
UL http://www.jneurosci.org/content/27/46/12611.abstract
AB Environmental temperature is an important factor exerting pervasive influence on neuronal morphology and synaptic physiology. In the Drosophila brain, axonal arborization of mushroom body Kenyon cells was enhanced when flies were raised at high temperature (30°C rather than 22°C) for several days. Isolated embryonic neurons in culture that lacked cell–cell contacts also displayed a robust temperature-induced neurite outgrowth. This cell-autonomous effect was reflected by significantly increased high-order branching and enlarged growth cones. The temperature-induced morphological alterations were blocked by the Na+ channel blocker tetrodotoxin and a Ca2+ channel mutation but could be mimicked by raising cultures at room temperature with suppressed K+ channel activity. Physiological analyses revealed increased inward Ca2+ currents and decreased outward K+ currents, in conjunction with a distal shift in the site of action potential initiation and increased prevalence of TTX-sensitive spontaneous Ca2+ transients. Importantly, the overgrowth caused by both temperature and hyperexcitability K+ channel mutations were sensitive to genetic perturbations of cAMP metabolism. Thus, temperature acts in a cell-autonomous manner to regulate neuronal excitability and spontaneous activity. Presumably, activity-dependent Ca2+ accumulation triggers the cAMP cascade to confer the activity-dependent plasticity of neuronal excitability and growth.