TY - JOUR
T1 - NOD-Rag2null IL-2Rγnull mice
T2 - An alternative to NOG mice for generation of humanized mice
AU - Katano, Ikumi
AU - Ito, Ryoji
AU - Kamisako, Tsutomu
AU - Eto, Tomoo
AU - Ogura, Tomoyuki
AU - Kawai, Kenji
AU - Suemizu, Hiroshi
AU - Takahashi, Takeshi
AU - Kawakami, Yutaka
AU - Ito, Mamoru
PY - 2014
Y1 - 2014
N2 - We have developed NOD-Rag2null IL-2Rγnull (NR2G) mice similar to NOD-scid IL-2Rγnull (NOG) mice that are known as an excellent host to generate humanized mice. To evaluate the usefulness of NR2G mice as a host for humanized mice, the engraftment rates and differentiation of human cells after human hematopoietic stem cell (HSC) transplantation were compared among NR2G, NOG, and NOD-scid mice. For this purpose, the appropriate irradiation doses to expand the niche for human stem cells in the bone marrow were first determined. As a result, 8 and 2.5 Gy in adult, and 4 and 1 Gy in newborn NR2G and NOG mice, respectively, were found to be appropriate. Next, 5 × 104 human umbilical cord blood CD34+ cells were intravenously inoculated into irradiated adult or newborn of the immunodeficient mice. These HSC transplantation experiments demonstrated that both NR2G and NOG mice showed high engraftment rates compared with NOD-scid mice, although NOG mice showed a slightly higher engraftment rate than that for NR2G mice. However, no difference was found in the human cell populations differentiated from HSCs between NR2G and NOG mice. The HSC transplantation experiments to adults and newborns of two immunodeficient mice also revealed that the HSC transplantation into newborn mice resulted in higher engraftment rate than those into adults. These results showed that NR2G mice could be used as an alternative host to NOG mice to generate humanized mice.
AB - We have developed NOD-Rag2null IL-2Rγnull (NR2G) mice similar to NOD-scid IL-2Rγnull (NOG) mice that are known as an excellent host to generate humanized mice. To evaluate the usefulness of NR2G mice as a host for humanized mice, the engraftment rates and differentiation of human cells after human hematopoietic stem cell (HSC) transplantation were compared among NR2G, NOG, and NOD-scid mice. For this purpose, the appropriate irradiation doses to expand the niche for human stem cells in the bone marrow were first determined. As a result, 8 and 2.5 Gy in adult, and 4 and 1 Gy in newborn NR2G and NOG mice, respectively, were found to be appropriate. Next, 5 × 104 human umbilical cord blood CD34+ cells were intravenously inoculated into irradiated adult or newborn of the immunodeficient mice. These HSC transplantation experiments demonstrated that both NR2G and NOG mice showed high engraftment rates compared with NOD-scid mice, although NOG mice showed a slightly higher engraftment rate than that for NR2G mice. However, no difference was found in the human cell populations differentiated from HSCs between NR2G and NOG mice. The HSC transplantation experiments to adults and newborns of two immunodeficient mice also revealed that the HSC transplantation into newborn mice resulted in higher engraftment rate than those into adults. These results showed that NR2G mice could be used as an alternative host to NOG mice to generate humanized mice.
KW - Humanized mice
KW - Immunodeficient mice
KW - NOG mice
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U2 - 10.1538/expanim.63.321
DO - 10.1538/expanim.63.321
M3 - Article
C2 - 25077762
AN - SCOPUS:84905183997
SN - 1341-1357
VL - 63
SP - 321
EP - 330
JO - Experimental Animals
JF - Experimental Animals
IS - 3
ER -