Name: Immunohistokemi af Drosophila larve til mikrotubulus visualisering
Uploaded: 2023-10-20T14:00:00
Description: Watch this Scientific Journal Video about Immunohistochemistry of Drosophila Larva for Microtubule Visualization at JoVE.com

immunohistochemistry of drosophila larva for microtubule visualization

Visning af mikrotubuli-netværk i Drosophila neuromuskulære kryds og muskelceller

Microtubules (MTs), as one of the structural components of the cytoskeleton, play an important role in diverse biological processes, including cell division, cell growth and motility, intracellular transport, and the maintenance of cell shape. Microtubule dynamics and function are modulated by interactions with other proteins, such as MAP1, MAP2, Tau, Katanin, and Kinesin1,2,3,4,5.
In neurons, microtubules are essential for the development and maintenance of axons and dendrites. Abnormalities in microtubules lead to dysfunction and even the death of neurons. For instance, in the brain of Alzheimer&#39;s patients, Tau protein hyperphosphorylation reduces the stability of the microtubule network, causing neurological irregularities6. Thus, examining microtubule networks will contribute to a comprehension of neurodevelopment and the pathogenesis of neurological diseases.
The neuromuscular junction (NMJ) is the peripheral synapse formed between a motor neuron axon terminal and a muscle fiber, which is an excellent and powerful model system for studying synaptic structure and functions7. Futsch is a protein in Drosophila that is homologous to the microtubule-binding protein MAP1B found in mammals8. It is expressed only in neurons and plays a role in the development of the NMJ&#39;s synaptic buttons8,9. In wild-type, filamentous bundles that run along the center of NMJ processes are visualized by immunostaining with anti-Futsch. When reaching NMJ&#39;s end, this bundle has the ability to either form a loop consisting of microtubules or to lose its filamentous structure, resulting in a diffuse and punctate appearance10. Microtubule loops are associated with paused growth cones, which suggests the microtubule array is stable11. Therefore, we can indirectly determine the stable microtubule development in NMJ by Futsch staining. The large size of muscle cells in Drosophila larva allows for clear visualization of the microtubule network. The factors affecting the stability of the microtubule network can be found by analyzing the density and shape of microtubules. Simultaneously, the microtubule network status of muscle cells can be cross-verified with the result of NMJ to obtain more comprehensive conclusions.
Many protocols have been employed for investigating the network and dynamics of microtubules. However, these researches have often focused on in vitro studies12,13,14,15,16. Alternatively, some in vivo experiments have employed electron microscopy to detect the cytoskeleton17. According to the specific binding of fluorescently labeled antibodies or chemical dyes to proteins or DNA, the methods presented here allow the detection of microtubule networks in NMJ at the level of individual neurons in vivo, with results corroborated by observations in muscle cells. This protocol is simple, stable, and repeatable when combined with the powerful genetic tools available in Drosophila melanogaster, enabling a diverse range of phenotypic examinations and genetic screenings for the role of microtubule network regulatory proteins in the nervous system in vivo.

Forfatter Spotlight: Forståelse af mikrotubuli-netværk i Drosophila neuromuskulære kryds 

Brug af Drosophila larve neuromuskulær junction og muskelceller til at visualisere mikrotubulus netværk

Currently, microtubule dynamics are observed indirectly through microtubule-binding proteins such as EB1. Since alphabeta tubulin heterodimers are abundant in the cytoplasm, fold directly, neighboring tubulin heterodimers are lacking the dynamics of microtubule networks in vivo. Our protocol visualizes microtubules in neuromuscular synapses and muscle cells.When combined with the powerful genetic tools available in Drosophila melanogaster, enabling a diverse range of phenotypic examinations and the genetic screening for the role of microtubule network regulatory proteins in the nervous system in vivo. Our research focuses on the relationship between the cytoskeleton and the neurodevelopment, as well as its implications for neurological diseases. We hope to discover the mechanism of neurodevelopment and the parthenogenesis for neurological diseases by highlighting the effect of cytoskeletal regulatory proteins on neurons.

Watch this Scientific Journal Video about Immunohistochemistry of Drosophila Larva for Microtubule Visualization at JoVE.com

Immunohistokemi af Drosophila larve til mikrotubulus visualisering

PBST fjernes og nedsænkes de paraformaldehydfikserede drosophila larvekroppe i et blokeringsmiddel i 40 minutter ved stuetemperatur. Udskift blokeringsmidlet med 200 mikroliter af det primære antistof fortyndet med 0,2% PBST. Lad larverne inkubere ved fire grader Celsius natten over.Den næste dag vaskes larverne med 0,2%PBST i 10 minutter. Fjern derefter PBST fra røret og tilsæt 200 mikroliter fortyndet sekundært antistof. Inkuber det ved omgivelsestemperatur i 1,5 timer i mørket.Indfør et nukleært farvestof såsom TO-PRO R3-iodid i inkubationsrøret i 30 minutter, mens mikrotubuli farves i mørket. Til sidst skylles det sekundære antistof og det nukleare farvestof af med 0,2% PBST i 10 minutter.