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@ARTICLE{Kilo:163366,
author = {Kilo, Lukas and Stürner, Tomke and Tavosanis, Gaia and
Ziegler, Anna B},
title = {{D}rosophila {D}endritic {A}rborisation {N}eurons:
{F}antastic {A}ctin {D}ynamics and {W}here to {F}ind
{T}hem.},
journal = {Cells},
volume = {10},
number = {10},
issn = {2073-4409},
address = {Basel},
publisher = {MDPI},
reportid = {DZNE-2022-00129},
pages = {2777},
year = {2021},
note = {(CC BY)},
abstract = {Neuronal dendrites receive, integrate, and process numerous
inputs and therefore serve as the neuron's 'antennae'.
Dendrites display extreme morphological diversity across
different neuronal classes to match the neuron's specific
functional requirements. Understanding how this structural
diversity is specified is therefore important for shedding
light on information processing in the healthy and diseased
nervous system. Popular models for in vivo studies of
dendrite differentiation are the four classes of dendritic
arborization (c1da-c4da) neurons of Drosophila larvae with
their class-specific dendritic morphologies. Using da
neurons, a combination of live-cell imaging and
computational approaches have delivered information on the
distinct phases and the time course of dendrite development
from embryonic stages to the fully developed dendritic tree.
With these data, we can start approaching the basic logic
behind differential dendrite development. A major role in
the definition of neuron-type specific morphologies is
played by dynamic actin-rich processes and the regulation of
their properties. This review presents the differences in
the growth programs leading to morphologically different
dendritic trees, with a focus on the key role of actin
modulatory proteins. In addition, we summarize requirements
and technological progress towards the visualization and
manipulation of such actin regulators in vivo.},
subtyp = {Review Article},
keywords = {Actins: metabolism / Animals / Cell Differentiation /
Dendrites: metabolism / Drosophila: metabolism / actin
(Other) / dendrite arborization (da) neurons (Other) /
neuronal dendrites (Other) / time-lapse imaging (Other) /
Actins (NLM Chemicals)},
cin = {AG Tavosanis},
ddc = {570},
cid = {I:(DE-2719)1013018},
pnm = {351 - Brain Function (POF4-351)},
pid = {G:(DE-HGF)POF4-351},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:34685757},
pmc = {pmc:PMC8534399},
doi = {10.3390/cells10102777},
url = {https://pub.dzne.de/record/163366},
}