mouse oocyte
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2022 ◽  
Vol 230 ◽  
pp. 113105
Author(s):  
Jian-Zhou Shang ◽  
Shi-Ru Li ◽  
Xiao-Qing Li ◽  
Yu-Ting Zhou ◽  
Xiang Ma ◽  
...  

2022 ◽  
Vol 77 (1) ◽  
pp. 33-34
Author(s):  
Clementina Cantatore ◽  
Jenny S. George ◽  
Raffaella Depalo ◽  
Giuseppe D'Amato ◽  
Molly Moravek ◽  
...  

Author(s):  
Yue Wang ◽  
Zhen-Nan Pan ◽  
Chun-Hua Xing ◽  
Hao-Lin Zhang ◽  
Shao-Chen Sun

2021 ◽  
Vol 36 (2) ◽  
Author(s):  
Jiaqi Zhang ◽  
Wenbo Liu ◽  
Guangyue Li ◽  
Chengpeng Xu ◽  
Xiaoqing Nie ◽  
...  

Cryobiology ◽  
2021 ◽  
Vol 103 ◽  
pp. 186
Author(s):  
Akshatha Daddangadi ◽  
Shubhashree Uppangala ◽  
Satish Kumar Adiga

2021 ◽  
Author(s):  
Anne Bourdais ◽  
Benoit Dehapiot ◽  
Guillaume Halet

How multiple actin networks coexist in a common cytoplasm, while competing for a shared pool of monomers, is still an ongoing question. This is exemplified by meiotic maturation in the mouse oocyte, which relies on the dynamic remodeling of distinct cortical and cytoplasmic F-actin networks. Here we show that the conserved actin-depolymerizing factor cofilin is activated in a switch-like manner at meiosis resumption from prophase arrest. Interfering with cofilin activation during maturation resulted in widespread microvilli elongation, while cytoplasmic F-actin was depleted, leading to defects in spindle migration and polar body extrusion. In contrast, cofilin inactivation in metaphase II-arrested oocytes resulted in a shutdown of F-actin dynamics, along with a dramatic overgrowth of the polarized actin cap. However, inhibition of the Arp2/3 complex to promote actin cap disassembly elicited ectopic microvilli outgrowth in the polarized cortex. These data establish cofilin as a key player in actin network homeostasis in oocytes, and reveal that microvilli can act as a sink for monomers upon disassembly of a competing network.


2021 ◽  
Author(s):  
Anne Bourdais ◽  
Benoit Dehapiot ◽  
Guillaume Halet

How multiple actin networks coexist in a common cytoplasm, while competing for a shared pool of monomers, is still an ongoing question. This is exemplified by meiotic maturation in the mouse oocyte, which relies on the dynamic remodeling of distinct cortical and cytoplasmic F-actin networks. Here we show that the conserved actin-depolymerizing factor cofilin is activated in a switch like manner at meiosis resumption from prophase arrest. Interfering with cofilin activation during maturation resulted in widespread microvilli elongation, while cytoplasmic F-actin was depleted, leading to defects in spindle migration and polar body extrusion. In contrast, cofilin inactivation in metaphase II-arrested oocytes resulted in a shutdown of F-actin dynamics, along with dramatic overgrowth of the polarized actin cap. However, inhibition of the Arp2/3 complex to promote actin cap disassembly elicited ectopic microvilli outgrowth in the polarized cortex. These data establish cofilin as a key player in actin network homeostasis in oocytes, and reveal that microvilli can act as a sink for monomers upon disassembly of a competing network.


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