TY - JOUR
T1 - APOA-1 is a Novel Marker of Erythroid Cell Maturation from Hematopoietic Stem Cells in Mice and Humans
AU - Inoue, Tomoko
AU - Sugiyama, Daisuke
AU - Kurita, Ryo
AU - Oikawa, Tatsuo
AU - Kulkeaw, Kasem
AU - Kawano, Hirotaka
AU - Miura, Yoshie
AU - Okada, Michiyo
AU - Suehiro, Youko
AU - Takahashi, Atsushi
AU - Marumoto, Tomotoshi
AU - Inoue, Hiroyuki
AU - Komatsu, Norio
AU - Tani, Kenzaburo
N1 - Funding Information:
Acknowledgements The authors would like to thank Chiyo Miz-uochi, Yuka Horio, Tatsuya Sasaki and Michiko Ushijima at Kyushu University for excellent technical assistance. This work was supported by a grant from the Project for Realization of Regenerative Medicine from the Ministry of Education, Culture, Sports, Science and Technology and by a grant from the BASIS project from the Ministry of Education, Culture, Sports, Science and Technology. T. Inoue is supported by research fellowships from the Japan Society for the Promotion of Science for Young Scientists.
PY - 2011/3
Y1 - 2011/3
N2 - The mechanism that regulates the terminal maturation of hematopoietic stem cells into erythroid cells is poorly understood. Therefore, identifying genes and surface markers that are restricted to specific stages of erythroid maturation will further our understanding of erythropoiesis. To identify genes expressed at discrete stages of erythroid development, we screened for genes that contributed to the proliferation and maturation of erythropoietin (EPO)-dependent UT-7/EPO cells. After transducing erythroid cells with a human fetal liver (FL)-derived lentiviral cDNA library and culturing the cells in the absence of EPO, we identified 17 candidate genes that supported erythroid colony formation. In addition, the mouse homologues of these candidate genes were identified and their expression was examined in E12. 5 erythroid populations by qRT-PCR. The expression of candidate erythroid marker was also assessed at the protein level by immunohistochemistry and ELISA. Our study demonstrated that expression of the Apoa-1 gene, an apolipoprotein family member, significantly increased as hematopoietic stem cells differentiated into mature erythroid cells in the mouse FL. The Apoa-1 protein was more abundant in mature erythroid cells than hematopoietic stem and progenitor cells in the mouse FL by ELISA. Moreover, APOA-1 gene expression was detected in mature erythroid cells from human peripheral blood. We conclude that APOA-1 is a novel marker of the terminal erythroid maturation of hematopoietic stem cells in both mice and humans.
AB - The mechanism that regulates the terminal maturation of hematopoietic stem cells into erythroid cells is poorly understood. Therefore, identifying genes and surface markers that are restricted to specific stages of erythroid maturation will further our understanding of erythropoiesis. To identify genes expressed at discrete stages of erythroid development, we screened for genes that contributed to the proliferation and maturation of erythropoietin (EPO)-dependent UT-7/EPO cells. After transducing erythroid cells with a human fetal liver (FL)-derived lentiviral cDNA library and culturing the cells in the absence of EPO, we identified 17 candidate genes that supported erythroid colony formation. In addition, the mouse homologues of these candidate genes were identified and their expression was examined in E12. 5 erythroid populations by qRT-PCR. The expression of candidate erythroid marker was also assessed at the protein level by immunohistochemistry and ELISA. Our study demonstrated that expression of the Apoa-1 gene, an apolipoprotein family member, significantly increased as hematopoietic stem cells differentiated into mature erythroid cells in the mouse FL. The Apoa-1 protein was more abundant in mature erythroid cells than hematopoietic stem and progenitor cells in the mouse FL by ELISA. Moreover, APOA-1 gene expression was detected in mature erythroid cells from human peripheral blood. We conclude that APOA-1 is a novel marker of the terminal erythroid maturation of hematopoietic stem cells in both mice and humans.
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U2 - 10.1007/s12015-010-9140-7
DO - 10.1007/s12015-010-9140-7
M3 - Article
C2 - 20376577
AN - SCOPUS:78751645501
SN - 1550-8943
VL - 7
SP - 43
EP - 52
JO - Stem Cell Reviews
JF - Stem Cell Reviews
IS - 1
ER -