Morita Yuichi, Sakata Naoaki, Nishimura Masuhiro, Kawakami Ryo, Shimizu Masayuki, Yoshimatsu Gumpei, Sawamoto Osamu, Matsumoto Shinichi, Wada Hideichi, Kodama Shohta
Department of Regenerative Medicine and Transplantation, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Center for Regenerative Medicine, Fukuoka University Hospital, Fukuoka, Japan.
Cell Transplant. 2024 Jan-Dec;33:9636897241260195. doi: 10.1177/09636897241260195.
Lymphedema is an intractable disease with few effective therapeutic options. Autologous mesenchymal stem cell (MSC) transplantation is a promising therapy for this disease. However, its use is limited by the cost and time for preparation. Recently, xenotransplantation of porcine MSCs has emerged as an alternative to autologous MSC transplantation. In this study, we aimed to clarify the usefulness of neonatal porcine bone marrow-derived MSC (NpBM-MSC) xenotransplantation for the treatment of lymphedema. One million NpBM-MSCs were xenotransplanted into the hind limbs of mice with severe lymphedema (MSC transplantation group). The therapeutic effects were assessed by measuring the femoral circumference, the volume of the hind limb, the number and diameter of lymphatic vessels in the hind limb, and lymphatic flow using a near-infrared fluorescence (NIRF) imaging system. We compared the effects using mice with lymphedema that did not undergo NpBM-MSC transplantation (negative control group). The condition of the transplanted NpBM-MSCs was also evaluated histologically. The femoral circumference and volume of the hind limb had been normalized by postoperative day (POD) 14 in the MSC transplantation group, but not in the negative control group ( = 0.041). NIRF imaging revealed that lymphatic flow had recovered in the MSC transplantation group by POD 14, as shown by an increase in luminance in the hind limb. Histological assessment also showed that the xenotransplantation of NpBM-MSC increased the proliferation of lymphatic vessels, but they had been rejected by POD 14. The xenotransplantation of NpBM-MSCs is an effective treatment for lymphedema, and this is mediated through the promotion of lymphangiogenesis.
淋巴水肿是一种难治性疾病,有效的治疗选择很少。自体间充质干细胞(MSC)移植是治疗这种疾病的一种有前景的疗法。然而,其应用受到制备成本和时间的限制。最近,猪MSC的异种移植已成为自体MSC移植的一种替代方法。在本研究中,我们旨在阐明新生猪骨髓来源的MSC(NpBM-MSC)异种移植治疗淋巴水肿的有效性。将100万个NpBM-MSCs异种移植到严重淋巴水肿小鼠的后肢(MSC移植组)。通过测量股骨周长、后肢体积、后肢淋巴管数量和直径以及使用近红外荧光(NIRF)成像系统测量淋巴流量来评估治疗效果。我们将其与未接受NpBM-MSC移植的淋巴水肿小鼠(阴性对照组)的效果进行了比较。还通过组织学评估移植的NpBM-MSCs的情况。在MSC移植组中,术后第14天(POD 14)股骨周长和后肢体积恢复正常,但在阴性对照组中未恢复正常(P = 0.041)。NIRF成像显示,到POD 14时,MSC移植组的淋巴流量已恢复,后肢亮度增加表明了这一点。组织学评估还显示,NpBM-MSC的异种移植增加了淋巴管的增殖,但到POD 14时它们已被排斥。NpBM-MSCs的异种移植是治疗淋巴水肿的有效方法,这是通过促进淋巴管生成介导的。