scholarly journals Actin dependent membrane polarization reveals the mechanical nature of the neuroblast polarity cycle

2021 ◽  
Author(s):  
Bryce LaFoya ◽  
Kenneth E. Prehoda

AbstractThe Par complex directs fate determinant segregation from the apical membrane of asymmetrically dividing Drosophila neuroblasts. While the physical interactions that recruit the Par complex have been extensively studied, little is known about how the membrane itself behaves during polarization. We examined the membrane dynamics of neuroblasts and surrounding cells with super-resolution imaging, revealing cellular-scale movements of diverse membrane features during asymmetric division cycles. Membrane domains that are distributed across the neuroblast membrane in interphase become polarized in early mitosis, where they mediate formation of cortical patches of the Par protein aPKC. Membrane and protein polarity cycles are precisely synchronized, and are generated by extensive actin dependent forces that deform the surrounding tissue. In addition to suggesting a role for the membrane in asymmetric division, our results reveal the mechanical nature of the neuroblast polarity cycle.

2009 ◽  
Vol 20 (1) ◽  
pp. 282-295 ◽  
Author(s):  
Weiqun Yu ◽  
Puneet Khandelwal ◽  
Gerard Apodaca

Epithelial cells respond to mechanical stimuli by increasing exocytosis, endocytosis, and ion transport, but how these processes are initiated and coordinated and the mechanotransduction pathways involved are not well understood. We observed that in response to a dynamic mechanical environment, increased apical membrane tension, but not pressure, stimulated apical membrane exocytosis and ion transport in bladder umbrella cells. The exocytic response was independent of temperature but required the cytoskeleton and the activity of a nonselective cation channel and the epithelial sodium channel. The subsequent increase in basolateral membrane tension had the opposite effect and triggered the compensatory endocytosis of added apical membrane, which was modulated by opening of basolateral K+ channels. Our results indicate that during the dynamic processes of bladder filling and voiding apical membrane dynamics depend on sequential and coordinated mechanotransduction events at both membrane domains of the umbrella cell.


2013 ◽  
Vol 104 (2) ◽  
pp. 652a ◽  
Author(s):  
Yuji Ishitsuka ◽  
Yiming Li ◽  
Reinhard Fischer ◽  
Norio Takeshita ◽  
G. Ulrich Nienhaus

Nanoscale ◽  
2015 ◽  
Vol 7 (8) ◽  
pp. 3373-3380 ◽  
Author(s):  
Junling Chen ◽  
Jing Gao ◽  
Jiazhen Wu ◽  
Min Zhang ◽  
Mingjun Cai ◽  
...  

N-GlcNAcs exist in irregular clusters on the apical membrane and most of these N-GlcNAc clusters are co-localized with lipid rafts by dSTORM imaging.


2021 ◽  
Vol 13 (10) ◽  
pp. 1956
Author(s):  
Jingyu Cong ◽  
Xianpeng Wang ◽  
Xiang Lan ◽  
Mengxing Huang ◽  
Liangtian Wan

The traditional frequency-modulated continuous wave (FMCW) multiple-input multiple-output (MIMO) radar two-dimensional (2D) super-resolution (SR) estimation algorithm for target localization has high computational complexity, which runs counter to the increasing demand for real-time radar imaging. In this paper, a fast joint direction-of-arrival (DOA) and range estimation framework for target localization is proposed; it utilizes a very deep super-resolution (VDSR) neural network (NN) framework to accelerate the imaging process while ensuring estimation accuracy. Firstly, we propose a fast low-resolution imaging algorithm based on the Nystrom method. The approximate signal subspace matrix is obtained from partial data, and low-resolution imaging is performed on a low-density grid. Then, the bicubic interpolation algorithm is used to expand the low-resolution image to the desired dimensions. Next, the deep SR network is used to obtain the high-resolution image, and the final joint DOA and range estimation is achieved based on the reconstructed image. Simulations and experiments were carried out to validate the computational efficiency and effectiveness of the proposed framework.


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