Volume 7, Issue 1 p. 32-38
Research Article

Three‐dimensional culture of mouse bone marrow cells on stroma formed within a porous scaffold: influence of scaffold shape and cryopreservation of the stromal layer on expansion of haematopoietic progenitor cells

Hirotoshi Miyoshi

Corresponding Author

Department of Biomedical Engineering, University of Tsukuba, Ibaraki, Japan

Hirotoshi Miyoshi, Department of Biomedical Engineering, Institute of Basic Medical Sciences, Graduate School of Comprehensive Human Sciences, University of Tsukuba, 1‐1‐1 Tennoudai, Tsukuba, Ibaraki 305–8575, Japan. E‐mail: hmiyoshi@md.tsukuba.ac.jpSearch for more papers by this author
Norio Ohshima

Department of Biomedical Engineering, University of Tsukuba, Ibaraki, Japan

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Chiaki Sato

Department of Biomedical Engineering, University of Tsukuba, Ibaraki, Japan

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First published: 14 November 2011
Citations: 10

Abstract

This study's primary goal was to develop an effective ex vivo expansion method for haematopoietic cells. 3D culture of mouse bone marrow cells was performed in porous scaffolds using a sheet or cube shape. Bone marrow cells were cultured on bone marrow‐derived stromal layers formed within the scaffolds and the effect of scaffold shape on the expansion of haematopoietic cells was examined. In some experiments, stromal layers within cubic scaffolds were frozen and then used to culture bone marrow cells after thawing. Results show that after comparison, total cell density and expansion of haematopoietic cells were greater in cultures using the cubic scaffold, suggesting that it was superior to the sheet‐like scaffold for expanding haematopoietic cells. When cryopreserved stroma was used, it effectively supported the expansion of haematopoietic cells, and a greater expansion of haematopoietic cells [(erythroid and haematopoietic progenitor cells (HPCs)] was achieved than in cultures with stromal cells that had not been cryopreserved. Expansion of cells using cryopreserved stroma had several other advantages such as a shorter culture period than the conventional method, a stable supply of stromal cells, and ease of handling and scaling up. As a result, this is an attractive method for ex vivo expansion of haematopoietic stem cells (HSCs) and HPCs for clinical use. Copyright © 2011 John Wiley & Sons, Ltd.

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