Faculty Opinions recommendation of Prolonged prometaphase blocks daughter cell proliferation despite normal completion of mitosis.

Author(s):  
Yves Barral
2014 ◽  
Vol 30 (2) ◽  
pp. 192-208 ◽  
Author(s):  
Magnus Baumgardt ◽  
Daniel Karlsson ◽  
Behzad Y. Salmani ◽  
Caroline Bivik ◽  
Ryan B. MacDonald ◽  
...  

eLife ◽  
2019 ◽  
Vol 8 ◽  
Author(s):  
Jesús Rodriguez Curt ◽  
Behzad Yaghmaeian Salmani ◽  
Stefan Thor

During CNS development, there is prominent expansion of the anterior region, the brain. In Drosophila, anterior CNS expansion emerges from three rostral features: (1) increased progenitor cell generation, (2) extended progenitor cell proliferation, (3) more proliferative daughters. We find that tailless (mouse Nr2E1/Tlx), otp/Rx/hbn (Otp/Arx/Rax) and Doc1/2/3 (Tbx2/3/6) are important for brain progenitor generation. These genes, and earmuff (FezF1/2), are also important for subsequent progenitor and/or daughter cell proliferation in the brain. Brain TF co-misexpression can drive brain-profile proliferation in the nerve cord, and can reprogram developing wing discs into brain neural progenitors. Brain TF expression is promoted by the PRC2 complex, acting to keep the brain free of anti-proliferative and repressive action of Hox homeotic genes. Hence, anterior expansion of the Drosophila CNS is mediated by brain TF driven ‘super-generation’ of progenitors, as well as ‘hyper-proliferation’ of progenitor and daughter cells, promoted by PRC2-mediated repression of Hox activity.


2017 ◽  
Vol 27 (8) ◽  
pp. 1161-1172 ◽  
Author(s):  
Ignacio Monedero Cobeta ◽  
Behzad Yaghmaeian Salmani ◽  
Stefan Thor

Development ◽  
2012 ◽  
Vol 139 (4) ◽  
pp. 678-689 ◽  
Author(s):  
C. Ulvklo ◽  
R. MacDonald ◽  
C. Bivik ◽  
M. Baumgardt ◽  
D. Karlsson ◽  
...  

PLoS Genetics ◽  
2016 ◽  
Vol 12 (4) ◽  
pp. e1005984 ◽  
Author(s):  
Caroline Bivik ◽  
Ryan B. MacDonald ◽  
Erika Gunnar ◽  
Khalil Mazouni ◽  
Francois Schweisguth ◽  
...  

Author(s):  
C. W. Kischer

The morphology of the fibroblasts changes markedly as the healing period from burn wounds progresses, through development of the hypertrophic scar, to resolution of the scar by a self-limiting process of maturation or therapeutic resolution. In addition, hypertrophic scars contain an increased cell proliferation largely made up of fibroblasts. This tremendous population of fibroblasts seems congruous with the abundance of collagen and ground substance. The fine structure of these cells should reflect some aspects of the metabolic activity necessary for production of the scar, and might presage the stage of maturation.A comparison of the fine structure of the fibroblasts from normal skin, different scar types, and granulation tissue has been made by transmission (TEM) and scanning electron microscopy (SEM).


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