Cotransplantation with MSCs improves engraftment of HSCs after autologous intra-bone marrow transplantation in nonhuman primates

• Published in: Experimental hematology Vol. 37; no. 10; pp. 1250 - 1257.e1
• Main Authors: Masuda, Shigeo, Ageyama, Naohide, Shibata, Hiroaki, Obara, Yoko, Ikeda, Tamako, Takeuchi, Kengo, Ueda, Yasuji, Ozawa, Keiya, Hanazono, Yutaka
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Inc 01-10-2009
• Subjects: Advanced Basic Science; Animals; Cell Lineage; Cells, Cultured - transplantation; Genes, Reporter; Genetic Vectors - analysis; Graft Survival; Hematology, Oncology and Palliative Medicine; Hematopoietic Stem Cell Transplantation - methods; Macaca fascicularis; Mesenchymal Stem Cell Transplantation; Mesenchymal Stromal Cells - physiology; Osteoblasts - cytology; Stromal Cells - transplantation; Transplantation Conditioning; Transplantation, Autologous
• ISSN: 0301-472X; 1873-2399
• DOI: 10.1016/j.exphem.2009.07.008

Objective Hematopoietic stem cells (HSCs) reside in the osteoblastic niche, which consists of osteoblasts. Mesenchymal stromal cells (MSCs) have an ability to differentiate into osteoblasts. Here, using nonhuman primates, we investigated the effects of cotransplantation with MSCs on the engraftment of HSCs after autologous intra-bone marrow transplantation. Materials and Methods From three cynomolgus monkeys, CD34-positive cells (as HSCs) and MSCs were obtained. The former were divided into two equal aliquots and each aliquot was genetically marked with a distinctive retroviral vector to track the in vivo fate. Each HSC aliquot with or without MSCs was autologously injected into the bone marrow (BM) cavity of right or left side, enabling the comparison of in vivo fates of the two HSC grafts in the same body. Results In the three monkeys, CD34+ cells transplanted with MSCs engrafted 4.4, 6.0, and 1.6 times more efficiently than CD34+ cells alone, as assessed by BM colony polymerase chain reaction. In addition, virtually all marked cells detected in the peripheral blood were derived from the cotransplantation aliquots. Notably, colony-forming units derived from the cotransplantation aliquots were frequently detected in BM distant sites from the injection site, implying that cotransplantation with MSCs also restored the ability of gene-marked HSCs to migrate and achieve homing in the distant BM. Conclusion Cotransplantation with MSCs would improve the efficacy of transplantation of gene-modified HSCs in primates, with enhanced engraftment in BM as well as increased chimerism in peripheral blood through migration and homing.