Prospectively Isolated Human Bone Marrow Cell‐Derived MSCs Support Primitive Human CD34‐Negative Hematopoietic Stem Cells

• Published in: Stem cells (Dayton, Ohio) Vol. 33; no. 5; pp. 1554 - 1565
• Main Authors: Matsuoka, Yoshikazu, Nakatsuka, Ryusuke, Sumide, Keisuke, Kawamura, Hiroshi, Takahashi, Masaya, Fujioka, Tatsuya, Uemura, Yasushi, Asano, Hiroaki, Sasaki, Yutaka, Inoue, Masami, Ogawa, Hiroyasu, Takahashi, Takayuki, Hino, Masayuki, Sonoda, Yoshiaki
• Format: Journal Article
• Language: English
• Published: United States Oxford University Press 01.05.2015
• Subjects: Adapalene - metabolism; Adipogenesis - genetics; Animals; Antigens, CD34 - metabolism; Biomarkers - metabolism; Bone marrow; Bone Marrow Cells - cytology; Bone Marrow Cells - metabolism; CD271; CD34‐negative; Cell Proliferation; Cell Separation - methods; Chondrogenesis - genetics; Colony-Forming Units Assay; Female; Fetal Blood - cytology; Flow Cytometry; Gene Expression Profiling; Gene Expression Regulation; Hematopoietic stem cell; Hematopoietic Stem Cells - cytology; Hematopoietic Stem Cells - metabolism; Humans; Mesenchymal stem/stromal cells; Mesenchymal Stromal Cells - cytology; Mesenchymal Stromal Cells - metabolism; Mice, Inbred NOD; Mice, SCID; Niche; Osteogenesis - genetics; SSEA‐4; Stage-Specific Embryonic Antigens - metabolism; Stem cells; Transplants & implants; Niche; CD34-negative; CD271; Hematopoietic stem cell; SSEA-4; Mesenchymal stem/stromal cells
• ISSN: 1066-5099; 1549-4918
• DOI: 10.1002/stem.1941

Hematopoietic stem cells (HSCs) are maintained in a specialized bone marrow (BM) niche, which consists of osteoblasts, endothelial cells, and a variety of mesenchymal stem/stromal cells (MSCs). However, precisely what types of MSCs support human HSCs in the BM remain to be elucidated because of their heterogeneity. In this study, we succeeded in prospectively isolating/establishing three types of MSCs from human BM‐derived lineage‐ and CD45‐negative cells, according to their cell surface expression of CD271 and stage‐specific embryonic antigen (SSEA)−4. Among them, the MSCs established from the Lineage−CD45−CD271+SSEA‐4+ fraction (DP MSC) could differentiate into osteoblasts and chondrocytes, but they lacked adipogenic differentiation potential. The DP MSCs expressed significantly higher levels of well‐characterized HSC‐supportive genes, including IGF‐2, Wnt3a, Jagged1, TGFβ3, nestin, CXCL12, and Foxc1, compared with other MSCs. Interestingly, these osteo‐chondrogenic DP MSCs possessed the ability to support cord blood‐derived primitive human CD34‐negative severe combined immunodeficiency‐repopulating cells. The HSC‐supportive actions of DP MSCs were partially carried out by soluble factors, including IGF‐2, Wnt3a, and Jagged1. Moreover, contact between DP MSCs and CD34‐positive (CD34+) as well as CD34‐negative (CD34−) HSCs was important for the support/maintenance of the CD34+/− HSCs in vitro. These data suggest that DP MSCs might play an important role in the maintenance of human primitive HSCs in the BM niche. Therefore, the establishment of DP MSCs provides a new tool for the elucidation of the human HSC/niche interaction in vitro as well as in vivo. Stem Cells 2015;33:1554–1565