Kawai Hotaka, Oo May Wathone, Takabatake Kiyofumi, Tosa Ikue, Soe Yamin, Eain Htoo Shwe, Sanou Sho, Fushimi Shigeko, Sukegawa Shintaro, Nakano Keisuke, Takeshi Takarada, Nagatsuka Hitoshi
Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Okayama University Okayama Japan.
Department of Regenerative Science, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Okayama University Okayama Japan.
JBMR Plus. 2023 Feb 11;7(3):e10722. doi: 10.1002/jbm4.10722. eCollection 2023 Mar.
Mesenchymal stem cell (MSC) therapy is a promising approach to curing bone diseases and disorders. In treating genetic bone disorders, MSC therapy is local or systemic transplantation of isolated and in vitro proliferated MSC rather than bone marrow transplantation. Recent evidence showed that bone marrow MSC engraftment to bone regeneration has been controversial in animal and human studies. Here, our modified bone marrow transplantation (BMT) method solved this problem. Like routine BMT, our modified method involves three steps: (i) isolation of bone marrow cells from the donor, (ii) whole-body lethal irradiation to the recipient, and (iii) injection of isolated bone marrow cells into irradiated recipient mice via the tail vein. The significant modification is imported at the bone marrow isolation step. While the bone marrow cells are flushed out from the bone marrow with the medium in routine BMT, we applied the enzymes' (collagenase type 4 and dispase) integrated medium to wash out the bone marrow cells. Then, cells were incubated in enzyme integrated solution at 37°C for 10 minutes. This modification designated BMT as collagenase-integrated BMT (c-BMT). Notably, successful engraftment of bone marrow MSC to the new bone formation, such as osteoblasts and chondrocytes, occurs in c-BMT mice, whereas routine BMT mice do not recruit bone marrow MSC. Indeed, flow cytometry data showed that c-BMT includes a higher proportion of LepR, CD51, or RUNX2 non-hematopoietic cells than BMT. These findings suggested that c-BMT is a time-efficient and more reliable technique that ensures the disaggregation and collection of bone marrow stem cells and engraftment of bone marrow MSC to the recipient. Hence, we proposed that c-BMT might be a promising approach to curing genetic bone disorders. © 2023 The Authors. published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.
间充质干细胞(MSC)疗法是治疗骨疾病和病症的一种有前景的方法。在治疗遗传性骨疾病时,MSC疗法是将分离并在体外增殖的MSC进行局部或全身移植,而非骨髓移植。最近的证据表明,在动物和人体研究中,骨髓MSC植入骨再生一直存在争议。在此,我们改良的骨髓移植(BMT)方法解决了这个问题。与常规BMT一样,我们改良的方法包括三个步骤:(i)从供体分离骨髓细胞,(ii)对受体进行全身致死性照射,(iii)通过尾静脉将分离的骨髓细胞注射到受照射的受体小鼠体内。显著的改良在骨髓分离步骤进行。在常规BMT中,骨髓细胞是用培养基从骨髓中冲洗出来的,而我们使用酶(IV型胶原酶和中性蛋白酶)混合培养基冲洗骨髓细胞。然后,细胞在酶混合溶液中于37°C孵育10分钟。这种改良将BMT命名为胶原酶整合BMT(c-BMT)。值得注意的是,在c-BMT小鼠中,骨髓MSC成功植入新骨形成部位,如成骨细胞和软骨细胞,而常规BMT小鼠则不会募集骨髓MSC。实际上,流式细胞术数据显示,c-BMT中LepR、CD51或RUNX2非造血细胞的比例高于BMT。这些发现表明,c-BMT是一种省时且更可靠的技术,可确保骨髓干细胞的解离和收集以及骨髓MSC植入受体。因此,我们提出c-BMT可能是治疗遗传性骨疾病的一种有前景的方法。© 2023作者。由Wiley Periodicals LLC代表美国骨与矿物质研究学会出版。