Literature DB >> 27462977

Bone Marrow Mesenchymal Stromal Cells from Clinical Scale Culture: In Vitro Evaluation of Their Differentiation, Hematopoietic Support, and Immunosuppressive Capacities.

Guadalupe R Fajardo-Orduña1,2, Héctor Mayani3, Marta E Castro-Manrreza4, Eugenia Flores-Figueroa5, Patricia Flores-Guzmán3, Lourdes Arriaga-Pizano6, Patricia Piña-Sánchez7, Erika Hernández-Estévez1, Andrés E Castell-Rodríguez8, Adriana K Chávez-Rueda9, María V Legorreta-Haquet9, Edelmiro Santiago-Osorio10, Juan J Montesinos1.   

Abstract

The differentiation capacity, hematopoietic support, and immunomodulatory properties of human bone marrow mesenchymal stromal cells (BM-MSCs) make them attractive therapeutic agents for a wide range of diseases. Clinical scale cultures (CSCs) have been used to expand BM-MSCs for their use in cell therapy protocols; however, little is known about the functionality of the expanded cells. The main goal of the present study was to evaluate the functional characteristics of BM-MSCs expanded from CSCs to determine the quality of the cells for cellular therapy protocols. To address this issue, we analyzed the morphology, immunophenotype, differentiation potential (adipogenic, osteogenic and chondrogenic), hematopoietic support, and immunosuppressive capacity of BM-MSCs from short scale cultures (SSCs) and CSCs in a comparative manner. After 12 days of culture in CSCs (HYPERFlask System), BM-MSCs reached cell numbers of 125.52 × 10(6) ± 25.6 × 10(6) MSCs, which corresponded to the number of cells required for transplantation (∼1.7 × 10(6) MSCs/kg for a 70-kg patient). After expansion, BM-MSCs expressed the characteristic markers CD73, CD90, and CD105; however, expansion decreased their differentiation capacity toward the adipogenic, osteogenic, and chondrogenic lineages and their ability to inhibit T-cell proliferation compared with SSCs-MSCs. Importantly, CSCs-MSCs maintained the ability to support the proliferation and expansion of hematopoietic progenitor cells and the capacity to express the molecules, cytokines, and extracellular matrix proteins involved in the regulation of hematopoiesis. Our study highlights the need to evaluate the functional properties of the expanded BM-MSCs for verification of their quality for cell therapy protocols.

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Year:  2016        PMID: 27462977     DOI: 10.1089/scd.2016.0071

Source DB:  PubMed          Journal:  Stem Cells Dev        ISSN: 1547-3287            Impact factor:   3.272


  3 in total

1.  Comparable osteogenic capacity of mesenchymal stem or stromal cells derived from human amnion membrane and bone marrow.

Authors:  Mehran Ghasemzadeh; Ehteramolsadat Hosseini; Mohammadhossein Ahmadi; Maedeh Kamalizad; Naser Amirizadeh
Journal:  Cytotechnology       Date:  2018-01-05       Impact factor: 2.058

2.  Coordinated metabolic transitions and gene expression by NAD+ during adipogenesis.

Authors:  Edgar Sánchez-Ramírez; Thi Phuong Lien Ung; Chiara Stringari; Lorena Aguilar-Arnal; Alejandro Alarcón Del Carmen; Ximena del Toro-Ríos; Guadalupe R Fajardo-Orduña; Lilia G Noriega; Victor A Cortés-Morales; Armando R Tovar; Juan José Montesinos; Ricardo Orozco-Solís
Journal:  J Cell Biol       Date:  2022-10-05       Impact factor: 8.077

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

Authors:  Guadalupe R Fajardo-Orduña; Héctor Mayani; Patricia Flores-Guzmán; Eugenia Flores-Figueroa; Erika Hernández-Estévez; Marta Castro-Manrreza; Patricia Piña-Sánchez; Lourdes Arriaga-Pizano; Alejandro Gómez-Delgado; Guadalupe Alarcón-Santos; Odette Balvanera-Ortíz; Juan J Montesinos
Journal:  Stem Cells Int       Date:  2017-11-09       Impact factor: 5.443

  3 in total

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