| Literature DB >> 30017246 |
Yukitaka Ito1, Sou Nakamura2, Naoshi Sugimoto2, Tomohiro Shigemori3, Yoshikazu Kato4, Mikiko Ohno5, Shinya Sakuma6, Keitaro Ito6, Hiroki Kumon6, Hidenori Hirose3, Haruki Okamoto3, Masayuki Nogawa7, Mio Iwasaki8, Shunsuke Kihara9, Kosuke Fujio2, Takuya Matsumoto2, Natsumi Higashi2, Kazuya Hashimoto2, Akira Sawaguchi10, Ken-Ichi Harimoto2, Masato Nakagawa8, Takuya Yamamoto11, Makoto Handa7, Naohide Watanabe7, Eiichiro Nishi5, Fumihito Arai6, Satoshi Nishimura12, Koji Eto13.
Abstract
The ex vivo generation of platelets from human-induced pluripotent cells (hiPSCs) is expected to compensate donor-dependent transfusion systems. However, manufacturing the clinically required number of platelets remains unachieved due to the low platelet release from hiPSC-derived megakaryocytes (hiPSC-MKs). Here, we report turbulence as a physical regulator in thrombopoiesis in vivo and its application to turbulence-controllable bioreactors. The identification of turbulent energy as a determinant parameter allowed scale-up to 8 L for the generation of 100 billion-order platelets from hiPSC-MKs, which satisfies clinical requirements. Turbulent flow promoted the release from megakaryocytes of IGFBP2, MIF, and Nardilysin to facilitate platelet shedding. hiPSC-platelets showed properties of bona fide human platelets, including circulation and hemostasis capacities upon transfusion in two animal models. This study provides a concept in which a coordinated physico-chemical mechanism promotes platelet biogenesis and an innovative strategy for ex vivo platelet manufacturing.Entities:
Keywords: IGFBP2; MIF; Nardilysin; bioreactor; iPSC; megakaryocyte; platelet; regenerative medicine; shear stress; turbulence
Mesh:
Year: 2018 PMID: 30017246 DOI: 10.1016/j.cell.2018.06.011
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582