骨髓
造血
体内
体外
细胞生物学
干细胞
造血干细胞
祖细胞
生物
免疫学
生物技术
生物化学
作者
Yu‐suke Torisawa,Catherine S. Spina,Tadanori Mammoto,Akiko Mammoto,James Weaver,Tracy Tat,James J. Collins,Donald E. Ingber
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2014-05-04
卷期号:11 (6): 663-669
被引量:395
摘要
Bone marrow formed in a cylindrical PDMS device implanted in a mouse can be surgically removed and cultured for a week in vitro without losing any of the hallmarks of in vivo bone marrow niches. Current in vitro hematopoiesis models fail to demonstrate the cellular diversity and complex functions of living bone marrow; hence, most translational studies relevant to the hematologic system are conducted in live animals. Here we describe a method for fabricating 'bone marrow–on–a–chip' that permits culture of living marrow with a functional hematopoietic niche in vitro by first engineering new bone in vivo, removing it whole and perfusing it with culture medium in a microfluidic device. The engineered bone marrow (eBM) retains hematopoietic stem and progenitor cells in normal in vivo–like proportions for at least 1 week in culture. eBM models organ-level marrow toxicity responses and protective effects of radiation countermeasure drugs, whereas conventional bone marrow culture methods do not. This biomimetic microdevice offers a new approach for analysis of drug responses and toxicities in bone marrow as well as for study of hematopoiesis and hematologic diseases in vitro.
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