Developmental Neurobiology

 
(insect neuron in co-culture with chicken neurons after pyrethroid application) 

Research activities


Developmental features of the brain development of Tenebrio molitor

The metamorphic development of holometabolous insects involves large-scale reorganizations of all tissues. Developmental studies demonstrate that the principle topological organization of the meal beetles mid-brain is not much affected by the drastic reorganizations during metamorphosis. The larval brain already shows most of the essential characteristics of the later adult one. We focussed our study to the development of specific neuropil regions as the so called central complex or the antennal lobe.
For an analysis of the neuroanatomical development we use classical silver impregnations, immunohistochemistry, specific injection techniques and ultramicroscopic analysis.
The characterization of identified neurons in the brain throughout development allows the description of morphological changes after application of neurotoxins in an in vivo assay.

Effect of pyrethroids on neurons from beetle and chicken
types of pyrethroidsPyrethroids are potent insecticides which are widely used in agriculture, disease vector control or in hosehold products. Many have a low toxicity against mammals, and a high toxicity against most arthropods.

To expand knowledge about the influence of the pyrethroids on neuronal development the metamorphic remodelling of the beetle brain is used as a modell for studying the formation and plasticity of nervous tissue.

For an analysis of the effect of pyrethroids on developing neuronal cells in vitro, we use cell cultures of embryonal chicken neurons and brain neurons from larval, prepupal and pupal stages of the beetle Tenebrio molitor.
 
 

Pattern formation of neurons in vitro

reaggregated embryonic chicken neuron of the cerebralhemispheres (stage 31), after 6d in a primary cell culture Brain neurons of embryonal chicken show a pattern formation in the cell culture by reaggregation of somata and fasciculation of neurites. After 5 days in culture those cells establish three diamensional clusters with internal differentiation. Our interest is due to the parameters changing or enhancing this tissue like organization.