Human Mesenchymal Stem/Stromal Cells from Umbilical Cord Blood and Placenta Exhibit Similar Capacities to Promote Expansion of Hematopoietic Progenitor Cells In Vitro

Author:

Fajardo-Orduña Guadalupe R.1,Mayani Héctor2,Flores-Guzmán Patricia2,Flores-Figueroa Eugenia3,Hernández-Estévez Erika1,Castro-Manrreza Marta4,Piña-Sánchez Patricia5,Arriaga-Pizano Lourdes6,Gómez-Delgado Alejandro7,Alarcón-Santos Guadalupe8,Balvanera-Ortíz Odette8,Montesinos Juan J.1ORCID

Affiliation:

1. Mesenchymal Stem Cells Laboratory, Oncology Research Unit, Oncology Hospital, National Medical Center, IMSS, Mexico City, Mexico

2. Hematopoietic Stem Cells Laboratory, Oncology Research Unit, Oncology Hospital, National Medical Center, IMSS, Mexico City, Mexico

3. Niche and Hematopoietic Microenvironment Laboratory, Oncology Research Unit, Oncology Hospital, National Medical Center, IMSS, Mexico City, Mexico

4. FES Zaragoza, National Autonomous University of Mexico, Mexico City, Mexico

5. Molecular Oncology Laboratory, Oncology Research Unit, Oncology Hospital, National Medical Center, IMSS, Mexico City, Mexico

6. Immunochemistry Research Unit, Specialties Hospital, National Medical Center “Siglo XXI”, IMSS, Mexico City, Mexico

7. Infectious and Parasitic Diseases, Medical Research Unit, Pediatric Hospital, National Medical Center, IMSS, Mexico City, Mexico

8. Troncoso General Hospital, IMSS, Mexico City, Mexico

Abstract

Mesenchymal stem/stromal cells (MSCs) from bone marrow (BM) have been used in coculture systems as a feeder layer for promoting the expansion of hematopoietic progenitor cells (HPCs) for hematopoietic cell transplantation. Because BM has some drawbacks, umbilical cord blood (UCB) and placenta (PL) have been proposed as possible alternative sources of MSCs. However, MSCs from UCB and PL sources have not been compared to determine which of these cell populations has the best capacity of promoting hematopoietic expansion. In this study, MSCs from UCB and PL were cultured under the same conditions to compare their capacities to support the expansion of HPCs in vitro. MSCs were cocultured with CD34+CD38Lin HPCs in the presence or absence of early acting cytokines. HPC expansion was analyzed through quantification of colony-forming cells (CFCs), long-term culture-initiating cells (LTC-ICs), and CD34+CD38Lin cells. MSCs from UCB and PL have similar capacities to increase HPC expansion, and this capacity is similar to that presented by BM-MSCs. Here, we are the first to determine that MSCs from UCB and PL have similar capacities to promote HPC expansion; however, PL is a better alternative source because MSCs can be obtained from a higher proportion of samples.

Funder

Fundación IMSS

Publisher

Hindawi Limited

Subject

Cell Biology,Molecular Biology

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