Reliable isolation of human mesenchymal stromal cells from bone marrow biopsy specimens in patients after allogeneic hematopoietic cell transplantation.


Journal

Cytotherapy
ISSN: 1477-2566
Titre abrégé: Cytotherapy
Pays: England
ID NLM: 100895309

Informations de publication

Date de publication:
01 2020
Historique:
received: 28 08 2019
revised: 25 10 2019
accepted: 28 10 2019
pubmed: 31 12 2019
medline: 4 8 2020
entrez: 30 12 2019
Statut: ppublish

Résumé

Isolation of mesenchymal stromal cells (MSCs) from pretreated, hematologic patients is challenging. Especially after allogeneic hematopoietic cell transplantation (HCT), standard protocols using bone marrow aspirates fail to reliably recover sufficient cell numbers. Because MSCs are considered to contribute to processes that mainly affect the outcome after transplantation, such as an efficient lymphohematopoietic recovery, extent of graft-versus-host disease as well as the occurrence of leukemic relapse, it is of great clinical relevance to investigate MSC function in this context. Previous studies showed that MSCs can be isolated by collagenase digestion of large bone fragments of hematologically healthy patients undergoing hip replacement or knee surgeries. We have now further developed this procedure for the isolation of MSCs from hematologic patients after allogeneic HCT by using trephine biopsy specimens obtained during routine examinations. Comparison of aspirates and trephine biopsy specimens from patients after allogeneic HCT revealed a significantly higher frequency of clonogenic MSCs (colony-forming unit-fibroblast [CFU-F]) in trephine biopsy specimens (mean, 289.8 ± standard deviation 322.5 CFU-F colonies/1 × 10

Identifiants

pubmed: 31883948
pii: S1465-3249(19)30873-4
doi: 10.1016/j.jcyt.2019.10.012
pii:
doi:

Substances chimiques

Collagenases EC 3.4.24.-

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

21-26

Informations de copyright

Copyright © 2019 International Society for Cell and Gene Therapy. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The project was funded by the Deutsche Forschungsgemeinschaft (Clinician Scientist position and Seed grant within the Centre for Regenerative Therapies Dresden, www.crt-dresden.de). The authors have no conflicts of interest to disclose.

Auteurs

Thomas Krüger (T)

Department of Internal Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany; German Cancer Consortium (DKTK), Partner Site Dresden, and German Cancer Research Center (DKFZ), Heidelberg, Germany. Electronic address: thomas.krueger@uniklinikum-dresden.de.

Jan Moritz Middeke (JM)

Department of Internal Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany.

Friedrich Stölzel (F)

Department of Internal Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany.

Anke Mütherig (A)

Department of Internal Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany.

Catrin List (C)

Department of Internal Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany.

Kalina Brandt (K)

Department of Internal Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany.

Katharina Heidrich (K)

Department of Internal Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany.

Raphael Teipel (R)

Department of Internal Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany.

Rainer Ordemann (R)

Department of Internal Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany.

Ulrich Schuler (U)

Department of Internal Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany.

Uta Oelschlägel (U)

Department of Internal Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany.

Martin Wermke (M)

Department of Internal Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany; University Cancer Centrum (UCC), Early Clinical Trial Unit (ECTU), University Hospital Carl Gustav Carus, Dresden, Germany.

Martin Kräter (M)

Max Planck Institute for the Science of Light & Max-Planck-Zentrum für Physik und Medizin, Erlangen, Germany.

Maik Herbig (M)

Max Planck Institute for the Science of Light & Max-Planck-Zentrum für Physik und Medizin, Erlangen, Germany; Biotechnology Center, Center for Molecular and Cellular Bioengineering TU Dresden Tatzberg 47-49, Dresden, Germany.

Rebekka Wehner (R)

German Cancer Consortium (DKTK), Partner Site Dresden, and German Cancer Research Center (DKFZ), Heidelberg, Germany; Institute of Immunology, Faculty of Medicine Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany; National Center for Tumor Diseases (NCT), Partner Site Dresden, Dresden, Germany.

Marc Schmitz (M)

German Cancer Consortium (DKTK), Partner Site Dresden, and German Cancer Research Center (DKFZ), Heidelberg, Germany; Institute of Immunology, Faculty of Medicine Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany; National Center for Tumor Diseases (NCT), Partner Site Dresden, Dresden, Germany; Center for Regenerative Therapies (CRTD), Dresden, Germany.

Martin Bornhäuser (M)

Department of Internal Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany; German Cancer Consortium (DKTK), Partner Site Dresden, and German Cancer Research Center (DKFZ), Heidelberg, Germany; National Center for Tumor Diseases (NCT), Partner Site Dresden, Dresden, Germany; Center for Regenerative Therapies (CRTD), Dresden, Germany.

Malte von Bonin (M)

Department of Internal Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany; German Cancer Consortium (DKTK), Partner Site Dresden, and German Cancer Research Center (DKFZ), Heidelberg, Germany.

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Classifications MeSH