Mesenchymal stem cells induced regulatory dendritic cells from hemopoietic progenitor cells through Notch pathway and TGF-β synergistically

2020 ◽  
Vol 222 ◽  
pp. 49-57 ◽  
Author(s):  
Xiaojing Li ◽  
Yulei Dong ◽  
Han Yin ◽  
Zhanfeng Qi ◽  
Dawei Wang ◽  
...  
Blood ◽  
2005 ◽  
Vol 106 (5) ◽  
pp. 1581-1589 ◽  
Author(s):  
Marc Pellegrini ◽  
Sue Bath ◽  
Vanessa S. Marsden ◽  
David C. S. Huang ◽  
Donald Metcalf ◽  
...  

Abstract The role of caspase-8 and its adaptor Fas-associated death domain (FADD) in lymphocyte apoptosis is well defined, but their functions in other hemopoietic lineages are not clear. We were unable to generate transgenic mice expressing dominant inhibitors of FADD or caspase-8 in hemopoietic cells, possibly because their expression may have precluded production of vital hemopoietic cells. When using a retroviral gene delivery system, fetal liver stem cells expressing a dominant-negative mutant of FADD (FADD-DN) were unable to generate myeloid or lymphoid cells upon transplantation into lethally irradiated mice. However, fetal liver stem cells expressing very low levels of the caspase-8 inhibitor cytokine response modifier A (CrmA) could reconstitute the hemopoietic system. This level of CrmA expression provided some protection against Fas ligand (FasL)–induced apoptosis and promoted accumulation of myeloid cells in the bone marrow, but it did not inhibit mitogen-induced proliferation of B or T lymphocytes. Using an in vitro colony formation assay, we found that fetal liver stem cells expressing FADD-DN, CrmA, or a dominant-negative mutant of caspase-8 could not proliferate in response to cytokine stimulation. These data demonstrate that the enzymatic activity of caspase-8 and its adaptor FADD are required for cytokine-induced proliferation of hemopoietic progenitor cells.


Gut and Liver ◽  
2018 ◽  
Vol 12 (6) ◽  
pp. 664-673 ◽  
Author(s):  
Hannah Jo ◽  
Young Woo Eom ◽  
Hyun-Soo Kim ◽  
Hong Jun Park ◽  
Hee Man Kim ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Brian I. Shaw ◽  
Jeffrey R. Ord ◽  
Chloe Nobuhara ◽  
Xunrong Luo

Donor specific transfusions have been the basis of tolerance inducing protocols since Peter Medawar showed that it was experimentally feasible in the 1950s. Though trials of cellular therapies have become increasingly common in solid organ transplantation, they have not become standard practice. Additionally, whereas some protocols have focused on cellular therapies as a method for donor antigen delivery—thought to promote tolerance in and of itself in the correct immunologic context—other approaches have alternatively focused on the intrinsic immunosuppressive properties of the certain cell types with less emphasis on their origin, including mesenchymal stem cells, regulatory T cells, and regulatory dendritic cells. Regardless of intent, all cellular therapies must contend with the potential that introducing donor antigen in a new context will lead to sensitization. In this review, we focus on the variety of cellular therapies that have been applied in human trials and non-human primate models, describe their efficacy, highlight data regarding their potential for sensitization, and discuss opportunities for cellular therapies within our current understanding of the immune landscape.


Diabetologia ◽  
2015 ◽  
Vol 59 (2) ◽  
pp. 325-333 ◽  
Author(s):  
Enrica Favaro ◽  
Andrea Carpanetto ◽  
Cristiana Caorsi ◽  
Mirella Giovarelli ◽  
Costanza Angelini ◽  
...  

2011 ◽  
Vol 41 (2) ◽  
pp. 183-198 ◽  
Author(s):  
Zhi-Gang Zhao ◽  
Wen Xu ◽  
Li Sun ◽  
Yong You ◽  
Fang Li ◽  
...  

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