Dynamic behavior of endoplasmic reticulum in living cells

Cell ◽  
1988 ◽  
Vol 54 (1) ◽  
pp. 37-46 ◽  
Author(s):  
Christopher Lee ◽  
Lan Bo Chen
2022 ◽  
pp. 132382
Author(s):  
Xiao-Chuang Chang ◽  
Xue-Feng Han ◽  
Bing-Jie Liu ◽  
Zi-Yi Jiang ◽  
Shuai-Ze Li ◽  
...  

2020 ◽  
Vol 44 (42) ◽  
pp. 18389-18398
Author(s):  
Qiujuan Ma ◽  
Chunyan Wang ◽  
Guojiang Mao ◽  
Meiju Tian ◽  
Jingguo Sun ◽  
...  

A novel reticulum-targeting and ratiometric fluorescent probe for determining hypochlorous acid has been developed.


2020 ◽  
Vol 92 (14) ◽  
pp. 9982-9988 ◽  
Author(s):  
Wei Shu ◽  
Shunping Zang ◽  
Chong Wang ◽  
Mengxu Gao ◽  
Jing Jing ◽  
...  

2018 ◽  
Vol 101 (11) ◽  
pp. e1800165 ◽  
Author(s):  
Elias A. Halabi ◽  
Salome Püntener ◽  
Pablo Rivera-Fuentes

Sensors ◽  
2020 ◽  
Vol 20 (13) ◽  
pp. 3653
Author(s):  
Denis Antonets ◽  
Nikolai Russkikh ◽  
Antoine Sanchez ◽  
Victoria Kovalenko ◽  
Elvira Bairamova ◽  
...  

In vitro cellular models are promising tools for studying normal and pathological conditions. One of their important applications is the development of genetically engineered biosensor systems to investigate, in real time, the processes occurring in living cells. At present, there are fluorescence, protein-based, sensory systems for detecting various substances in living cells (for example, hydrogen peroxide, ATP, Ca2+ etc.,) or for detecting processes such as endoplasmic reticulum stress. Such systems help to study the mechanisms underlying the pathogenic processes and diseases and to screen for potential therapeutic compounds. It is also necessary to develop new tools for the processing and analysis of obtained microimages. Here, we present our web-application CellCountCV for automation of microscopic cell images analysis, which is based on fully convolutional deep neural networks. This approach can efficiently deal with non-convex overlapping objects, that are virtually inseparable with conventional image processing methods. The cell counts predicted with CellCountCV were very close to expert estimates (the average error rate was < 4%). CellCountCV was used to analyze large series of microscopic images obtained in experimental studies and it was able to demonstrate endoplasmic reticulum stress development and to catch the dose-dependent effect of tunicamycin.


2020 ◽  
Vol 30 (6) ◽  
pp. 1357-1364
Author(s):  
Lei Zhou ◽  
Yunxia Li ◽  
Aiqin Zhou ◽  
Guanghui Zhang ◽  
Zhi-Qiang Cheng ◽  
...  

2018 ◽  
Vol 10 (47) ◽  
pp. 5702-5706 ◽  
Author(s):  
Nan Zhang ◽  
Baoli Dong ◽  
Xiuqi Kong ◽  
Wenhui Song ◽  
Weiying Lin

The pH changes of the endoplasmic reticulum (ER) are closely related to many diseases.


EMBO Reports ◽  
2002 ◽  
Vol 3 (12) ◽  
pp. 1188-1194 ◽  
Author(s):  
Matthias Becker ◽  
Christopher Baumann ◽  
Sam John ◽  
Dawn A. Walker ◽  
Marc Vigneron ◽  
...  

2008 ◽  
Vol 410 (3) ◽  
pp. 463-472 ◽  
Author(s):  
Jesper S. Hansen ◽  
Nils J. Færgeman ◽  
Birthe B. Kragelund ◽  
Jens Knudsen

In the present study, we microinjected fluorescently labelled liver bovine ACBP (acyl-CoA-binding protein) [FACI-50 (fluorescent acyl-CoA indicator-50)] into HeLa and BMGE (bovine mammary gland epithelial) cell lines to characterize the localization and dynamics of ACBP in living cells. Results showed that ACBP targeted to the ER (endoplasmic reticulum) and Golgi in a ligand-binding-dependent manner. A variant Y28F/K32A-FACI-50, which is unable to bind acyl-CoA, did no longer show association with the ER and became segregated from the Golgi, as analysed by intensity correlation calculations. Depletion of fatty acids from cells by addition of FAFBSA (fatty-acid-free BSA) significantly decreased FACI-50 association with the Golgi, whereas fatty acid overloading increased Golgi association, strongly supporting that ACBP associates with the Golgi in a ligand-dependent manner. FRAP (fluorescence recovery after photobleaching) showed that the fatty-acid-induced targeting of FACI-50 to the Golgi resulted in a 5-fold reduction in FACI-50 mobility. We suggest that ACBP is targeted to the ER and Golgi in a ligand-binding-dependent manner in living cells and propose that ACBP may be involved in vesicular trafficking.


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