Optimization of a flow cytometry‐based protocol for detection and phenotypic characterization of multipotent mesenchymal stromal cells from human bone marrow

Abstract

Background: To study the biology of rare bone marrow (BM) multipotent mesenchymal stromal cells (MSCs), recognized protocols are needed. Colony‐forming unit‐fibroblast (CFU‐F) assays have historically been used for the enumeration of MSCs. However, the need to isolate and further analyze MSCs requires new strategies based on cell surface markers. The purpose of this work was to verify the phenotype of BM MSCs in vivo and to develop flow cytometry‐based methods for their evaluation. Methods: Pre‐enrichment with D7‐FIB‐conjugated microbeads, cell sorting for CD45 low D7‐FIB+LNGFR+ cells, and CFU‐F assay were used to confirm the phenotype of BM MSCs in vivo. Further phenotypic characterization of MSCs was performed using three‐color flow cytometry following pre‐enrichment or by direct four‐color flow cytometry. The sensitivity of direct flow cytometry/rare event analysis for the accurate enumeration of MSCs was validated using 85 samples from patients with neoplastic BM diseases. Results: In normal BM, a significant correlation was found between the frequencies of CFU‐Fs and CD45 low D7‐FIB+LNGFR+ cells (n = 19, R = 0.719, P = 0.001). Following cell sorting, ˜15% of these cells were clonogenic. The same cells were enriched using LNGFR‐based positive selection, CD45/Glycophorin A‐based depletion, or plastic adherence. CD45 low D7‐FIB+LNGFR+ cells expressed classic makers of cultured MSCs CD73/SH3 and CD105/SH2 and markers of stromal reticular cells CD106/VCAM and alkaline phosphatase. Novel markers were identified including leukemia inhibitory factor receptor and gp130. CD45 low D7‐FIB+LNGFR+ cells were increased fourfold in the floating fat fraction of normal BM aspirates. Their frequency was decreased in chronic lymphocytic leukemia (threefold, n = 13, P = 0.049) and chronic myelogenous leukemia (ninefold, n = 11, P = 0.001) compared with that in age‐matched controls (n = 26 and n = 31, respectively). Conclusions: This study demonstrates the usefulness of flow cytometry‐based methods for the detection, enumeration and further phenotypic analysis of BM MSCs. These findings have broad applications for the future evaluation of BM MSCs in health and disease. © 2006 International Society for Analytical Cytology