Angiotensin II modulates the murine hematopoietic stem cell (HSC) and progenitors co‐cultured with stromal S17 cells

Author(s):  
Maíra Maftoum Costa ◽  
Roberta Sessa Stilhano ◽  
Carlos Rocha Oliveira ◽  
Chistiano Marcello Vaz Barbosa ◽  
Gustavo JS Pereira ◽  
...  
Haematologica ◽  
2019 ◽  
Vol 104 (9) ◽  
pp. 1744-1755 ◽  
Author(s):  
Laura Crisafulli ◽  
Sharon Muggeo ◽  
Paolo Uva ◽  
Yulei Wang ◽  
Masayuki Iwasaki ◽  
...  

Haematologica ◽  
2012 ◽  
Vol 97 (9) ◽  
pp. 1291-1294 ◽  
Author(s):  
O. Bereshchenko ◽  
E. Mancini ◽  
L. Luciani ◽  
A. Gambardella ◽  
C. Riccardi ◽  
...  

PLoS ONE ◽  
2016 ◽  
Vol 11 (7) ◽  
pp. e0158369 ◽  
Author(s):  
Alexandra Rundberg Nilsson ◽  
Shamit Soneji ◽  
Sofia Adolfsson ◽  
David Bryder ◽  
Cornelis Jan Pronk

1985 ◽  
Vol 459 (1 Hematopoietic) ◽  
pp. 221-231 ◽  
Author(s):  
K.-H. V. WANGENHEIM ◽  
H.P, PETERSON, ◽  
G. E. HÜBNER ◽  
L. E. FEINENDEGEN

2016 ◽  
Vol 213 (3) ◽  
pp. 433-449 ◽  
Author(s):  
Per Holmfeldt ◽  
Miguel Ganuza ◽  
Himangi Marathe ◽  
Bing He ◽  
Trent Hall ◽  
...  

Understanding the molecular regulation of hematopoietic stem and progenitor cell (HSPC) engraftment is paramount to improving transplant outcomes. To discover novel regulators of HSPC repopulation, we transplanted >1,300 mice with shRNA-transduced HSPCs within 24 h of isolation and transduction to focus on detecting genes regulating repopulation. We identified 17 regulators of HSPC repopulation: Arhgef5, Armcx1, Cadps2, Crispld1, Emcn, Foxa3, Fstl1, Glis2, Gprasp2, Gpr56, Myct1, Nbea, P2ry14, Smarca2, Sox4, Stat4, and Zfp521. Knockdown of each of these genes yielded a loss of function, except in the cases of Armcx1 and Gprasp2, whose loss enhanced hematopoietic stem cell (HSC) repopulation. The discovery of multiple genes regulating vesicular trafficking, cell surface receptor turnover, and secretion of extracellular matrix components suggests active cross talk between HSCs and the niche and that HSCs may actively condition the niche to promote engraftment. We validated that Foxa3 is required for HSC repopulating activity, as Foxa3−/− HSC fails to repopulate ablated hosts efficiently, implicating for the first time Foxa genes as regulators of HSPCs. We further show that Foxa3 likely regulates the HSC response to hematologic stress. Each gene discovered here offers a window into the novel processes that regulate stable HSPC engraftment into an ablated host.


2018 ◽  
Vol 8 (1) ◽  
Author(s):  
Jin Li ◽  
Carmen Carrillo García ◽  
Tamara Riedt ◽  
Maria Brandes ◽  
Sabrina Szczepanski ◽  
...  

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