Notch-Induced hIL-6 Production Facilitates the Maintenance of Self-Renewal of hCD34(+) Cord Blood Cells Through the Activation of Jak-PI3K-STAT3 Pathway

作者：Choi Bongkum; Chun Eunyoung; Kim So Yong; Kim Miyoung; Lee Ki Young^*; Kim Sung Joo

来源：American Journal Of Pathology, 2012, 180(1): 351-364.

DOI：10.1016/j.ajpath.2011.09.030

Ex vivo expansion of CD34(+) stern cells in contact culture between hCD34(+)CD38(-)Lin(-) cord blood stern cells and human delta-like-expressing AFT024 feeder cells revealed increased amounts of sternness-related proteins such as HoxB4, GATA2, Bmi-1, and p21 and anti-apoptotic proteins such as Bcl-2, Bcl-xL, Mcl-1, and phospho-Bad, when compared with control or noncontact culture. Production of human IL-6 (hIL-6) was markedly elevated in the culture, but was profoundly inhibited by treatment with gamma-secretase inhibitor. In addition, Notch-induced activation of STAT3 was directly involved in gene expression of hIL-6 and soluble hIL-6R alpha, indicating the close linkage between Notch signaling and hIL-6 production. Furthermore, depletion of soluble hIL-6 (with hIL-6-specific antibodies) and inhibition of IL-6-mediated signals (with a Jak1 inhibitor and wortmannin) severely affected the maintenance of self-renewal of hCD34(+) cord blood cells. It was also observed that the ex vivo expanded CD34(+) cord blood cells were induced to reconstitute human immune cells in nonobese diabetic mice with severe combined immunodeficiency when compared with freshly isolated CD34(+) cord blood cells. Together, these results strongly demonstrate that Notch signaling in the %26quot;cell-to-cell contact%26quot; between hCD34(+) cord blood and delta-like-expressing AFT024 feeder cells facilitates maintenance of self-renewal of hCD34(+) cord blood cells through direct regulation of hIL-6 production. (Am Pathol 2012. 180:351-364; DOI:101016/j.ajpath.2011.09.030)

• 出版日期2012-1