scholarly journals Primary cilium remodeling mediates a cell signaling switch in differentiating neurons

2020 ◽  
Vol 6 (21) ◽  
pp. eabb0601 ◽  
Author(s):  
Gabriela Toro-Tapia ◽  
Raman M. Das

Cellular differentiation leads to the formation of specialized cell types and complex morphological variations. Often, differentiating cells transition between states by switching how they respond to the signaling environment. However, the mechanisms regulating these transitions are poorly understood. Differentiating neurons delaminate from the neuroepithelium through the regulated process of apical abscission, which mediates an acute loss of polarity and primary cilium disassembly. Using high-resolution live-cell imaging in chick neural tube, we show that these cells retain an Arl13b+ particle, which elongates and initiates intraflagellar trafficking as it transits toward the cell body, indicating primary cilium remodeling. Notably, disrupting cilia during and after remodeling inhibits axon extension and leads to axon collapse, respectively. Furthermore, cilium remodeling corresponds to a switch from a canonical to noncanonical cellular response to Shh. This work transforms our understanding of how cells can rapidly reinterpret signals to produce qualitatively different responses within the same tissue context.

Cells ◽  
2020 ◽  
Vol 9 (12) ◽  
pp. 2618
Author(s):  
Fanning Zeng ◽  
Valerie Beck ◽  
Sven Schuierer ◽  
Isabelle Garnier ◽  
Carole Manneville ◽  
...  

Genetic knock-in using homology-directed repair is an inefficient process, requiring the selection of few modified cells and hindering its application to primary cells. Here, we describe Homology independent gene Tagging (HiTag), a method to tag a protein of interest by CRISPR in up to 66% of transfected cells with one single electroporation. The technique has proven effective in various cell types and can be used to knock in a fluorescent protein for live cell imaging, to modify the cellular location of a target protein and to monitor the levels of a protein of interest by a luciferase assay in primary cells.


2016 ◽  
Vol 22 (2) ◽  
pp. 264-274 ◽  
Author(s):  
Zachary Schultzhaus ◽  
Laura Quintanilla ◽  
Angelyn Hilton ◽  
Brian D. Shaw

AbstractHyphal cells of filamentous fungi grow at their tips in a method analogous to pollen tube and root hair elongation. This process, generally referred to as tip growth, requires precise regulation of the actin cytoskeleton, and characterizing the various actin structures in these cell types is currently an active area of research. Here, the actin marker Lifeact was used to document actin dynamics in the filamentous fungus Aspergillus nidulans. Contractile double rings were observed at septa, and annular clusters of puncta were seen subtending growing hyphal tips, corresponding to the well-characterized subapical endocytic collar. However, Lifeact also revealed two additional structures. One, an apical array, was dynamic on the face opposite the tip, while a subapical web was dynamic on the apical face and was located several microns behind the growth site. Each was observed turning into the other over time, implying that they could represent different localizations of the same structure, although hyphae with a subapical web grew faster than those exhibiting an apical array. The subapical web has not been documented in any filamentous fungus to date, and is separate from the networks of F-actin seen in other tip-growing organisms surrounding septa or stationary along the plasmalemma.


Lab on a Chip ◽  
2011 ◽  
Vol 11 (3) ◽  
pp. 484-489 ◽  
Author(s):  
Guilhem Velve Casquillas ◽  
Chuanhai Fu ◽  
Mael Le Berre ◽  
Jeremy Cramer ◽  
Sebastien Meance ◽  
...  

2010 ◽  
Vol 38 (5) ◽  
pp. 1728-1740 ◽  
Author(s):  
Lawrence Huang ◽  
Pattie S. Mathieu ◽  
Brian P. Helmke

2014 ◽  
Vol 127 (10) ◽  
pp. 2145-2150 ◽  
Author(s):  
Abdelhalim Loukil ◽  
Manuela Zonca ◽  
Cosette Rebouissou ◽  
Véronique Baldin ◽  
Olivier Coux ◽  
...  

2011 ◽  
Vol 17 (3) ◽  
pp. 440-445 ◽  
Author(s):  
Steffen Lorenz ◽  
Stephanie Tomcin ◽  
Volker Mailänder

AbstractLabeling of organelles for microscopy is achieved generally by specific dyes that either accumulate in a cellular compartment such as cyanine dyes in mitochondria or are only fluorescent under specific conditions such as the low pH in the lysosome. Here we demonstrate that Cy5—a fluorescent molecule that does not enter cells by itself—can be loaded into cells by attaching a short oligonucleotide. This very inexpensive labeling procedure can be done in the presence of serum. Therefore, very sensitive cell types should also be amenable to this procedure, and longer observations can be achieved compared to other commercially available dyes as the labeling reagent does not need to be washed out. This also points to the pitfall of using fluorescently labeled oligonucleotides for live cell imaging where the oligonucleotide is supposed to detect a specific target sequence in its subcellular distribution.


2019 ◽  
Vol 10 (1) ◽  
pp. 29 ◽  
Author(s):  
Haoyu Li ◽  
Changliang Guo ◽  
Deborah Kim-Holzapfel ◽  
Weiyi Li ◽  
Yelena Altshuller ◽  
...  

2021 ◽  
Author(s):  
Max Schelski ◽  
Frank Bradke

In developing vertebrate neurons, a neurite is formed by more than a hundred microtubules. While individual microtubules are dynamic, the microtubule array itself has been regarded as stationary. Using live cell imaging in combination with photoconversion techniques and pharmacological manipulations, we uncovered that the microtubule array flows retrogradely within neurites to the soma. This microtubule retrograde flow drives cycles of microtubule density, a hallmark of the fluctuating state before axon formation. Shortly after axon formation, microtubule retrograde flow slows down in the axon, which stabilizes microtubule density cycles and thereby functions as a molecular wedge to enable axon extension. We propose microtubule retrograde flow and its specific slowdown in the axon to be the long-sought mechanism to single one neurite out to drive neuronal polarization.


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