Long-Term Tolerance in a Murine Model of Type I Allergy Through Transplantation of Genetically Modified Hematopoietic Stem Cells

2007 ◽  
Vol 123 ◽  
pp. S77
Author(s):  
Ulrike Baranyi ◽  
Birgit Linhart ◽  
Nina Pilat ◽  
John Iacomini ◽  
Jessamyn Bagely ◽  
...  
2008 ◽  
Vol 180 (12) ◽  
pp. 8168-8175 ◽  
Author(s):  
Ulrike Baranyi ◽  
Birgit Linhart ◽  
Nina Pilat ◽  
Martina Gattringer ◽  
Jessamyn Bagley ◽  
...  

2009 ◽  
Vol 174 (5) ◽  
pp. 1808-1817 ◽  
Author(s):  
Caroline Soulas ◽  
Robert E. Donahue ◽  
Cynthia E. Dunbar ◽  
Derek A. Persons ◽  
Xavier Alvarez ◽  
...  

Blood ◽  
2012 ◽  
Vol 120 (1) ◽  
pp. 166-172 ◽  
Author(s):  
Ann Mullally ◽  
Luke Poveromo ◽  
Rebekka K. Schneider ◽  
Fatima Al-Shahrour ◽  
Steven W. Lane ◽  
...  

Abstract In the current model of the pathogenesis of polycythemia vera (PV), the JAK2V617F mutation arises in hematopoietic stem cells (HSCs) that maintain the disease, while erythroid precursor populations expand, resulting in excessive red blood cell production. We examined the role of these specific cell populations using a conditional Jak2V617F knockin murine model. We demonstrate that the most immature long-term (LT) HSCs are solely responsible for initiating and maintaining the disease in vivo and that Jak2V617F mutant LT-HSCs dominate hematopoiesis over time. When we induced Jak2V617F expression in erythropoietin receptor expressing precursor cells, the mice developed elevated hematocrit, expanded erythroid precursors, and suppressed erythropoietin levels. However, the disease phenotype was significantly attenuated compared with mice expressing Jak2V617F in LT-HSCs. In addition to developing a PV phenotype, all mice transplanted with Jak2V617F LT-HSCs underwent myelofibrotic transformation over time. These findings recapitulate the development of post-PV myelofibrosis in human myeloproliferative neoplasms. In aggregate, these results demonstrate the distinct roles of LT-HSCs and erythroid precursors in the pathogenesis of PV.


Author(s):  
Fatima Aerts-Kaya

: In contrast to their almost unlimited potential for expansion in vivo and despite years of dedicated research and optimization of expansion protocols, the expansion of Hematopoietic Stem Cells (HSCs) in vitro remains remarkably limited. Increased understanding of the mechanisms that are involved in maintenance, expansion and differentiation of HSCs will enable the development of better protocols for expansion of HSCs. This will allow procurement of HSCs with long-term engraftment potential and a better understanding of the effects of the external influences in and on the hematopoietic niche that may affect HSC function. During collection and culture of HSCs, the cells are exposed to suboptimal conditions that may induce different levels of stress and ultimately affect their self-renewal, differentiation and long-term engraftment potential. Some of these stress factors include normoxia, oxidative stress, extra-physiologic oxygen shock/stress (EPHOSS), endoplasmic reticulum (ER) stress, replicative stress, and stress related to DNA damage. Coping with these stress factors may help reduce the negative effects of cell culture on HSC potential, provide a better understanding of the true impact of certain treatments in the absence of confounding stress factors. This may facilitate the development of better ex vivo expansion protocols of HSCs with long-term engraftment potential without induction of stem cell exhaustion by cellular senescence or loss of cell viability. This review summarizes some of available strategies that may be used to protect HSCs from culture-induced stress conditions.


Author(s):  
Thao Trinh ◽  
James Ropa ◽  
Arafat Aljoufi ◽  
Scott Cooper ◽  
Anthony Sinn ◽  
...  

2013 ◽  
Vol 11 (1) ◽  
pp. 625-633 ◽  
Author(s):  
Philippe Brunet de la Grange ◽  
Marija Vlaski ◽  
Pascale Duchez ◽  
Jean Chevaleyre ◽  
Veronique Lapostolle ◽  
...  

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