Your browser doesn't support javascript.
loading
Transplantation Induces Profound Changes in the Transcriptional Asset of Hematopoietic Stem Cells: Identification of Specific Signatures Using Machine Learning Techniques.
Cilloni, Daniela; Petiti, Jessica; Campia, Valentina; Podestà, Marina; Squillario, Margherita; Montserrat, Nuria; Bertaina, Alice; Sabatini, Federica; Carturan, Sonia; Berger, Massimo; Saglio, Francesco; Bandini, Giuseppe; Bonifazi, Francesca; Fagioli, Franca; Moretta, Lorenzo; Saglio, Giuseppe; Verri, Alessandro; Barla, Annalisa; Locatelli, Franco; Frassoni, Francesco.
Afiliação
  • Cilloni D; Department of Clinical and Biological Sciences, University of Turin, 10043 Turin, Italy.
  • Petiti J; Department of Clinical and Biological Sciences, University of Turin, 10043 Turin, Italy.
  • Campia V; Department of Clinical and Biological Sciences, University of Turin, 10043 Turin, Italy.
  • Podestà M; Department of Pediatric Hemato-Oncology and Stem Cell and Cellular Therapy Laboratory, Institute G. Gaslini, Largo G Gaslini, 16147 Genova, Italy.
  • Squillario M; Department of Informatics, Bioengineering, Robotics and Systems Engineering, University of Genoa, via Dodecaneso 35, 16146 Genoa, Italy.
  • Montserrat N; Pluripotent Stem Cells and Activation of Endogenous Tissue Programs for Organ Regeneration (PR Lab), Institute for Bioengineering of Catalonia (IBEC) c/Baldiri Reixac 15-21, 08028 Barcelona, Spain.
  • Bertaina A; CIBER of Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), 28029 Barcelona, Spain.
  • Sabatini F; Department of Pediatric Hematology and Oncology IRCCS; Ospedale Pediatrico Bambino Gesù, Rome, University of Pavia, 27100 Pavia, Italy.
  • Carturan S; Department of Pediatric Hemato-Oncology and Stem Cell and Cellular Therapy Laboratory, Institute G. Gaslini, Largo G Gaslini, 16147 Genova, Italy.
  • Berger M; Department of Clinical and Biological Sciences, University of Turin, 10043 Turin, Italy.
  • Saglio F; Pediatric Onco-Hematology, Stem Cell Transplantation and Cellular Therapy Divisions, Regina Margherita Children Hospital, 10126 Turin, Italy.
  • Bandini G; Pediatric Onco-Hematology, Stem Cell Transplantation and Cellular Therapy Divisions, Regina Margherita Children Hospital, 10126 Turin, Italy.
  • Bonifazi F; Azienda Universitaria Ospedaliera di Bologna, Policlinico S. Orsola-Malpighi, 40138 Bologna, Italy.
  • Fagioli F; Azienda Universitaria Ospedaliera di Bologna, Policlinico S. Orsola-Malpighi, 40138 Bologna, Italy.
  • Moretta L; Pediatric Onco-Hematology, Stem Cell Transplantation and Cellular Therapy Divisions, Regina Margherita Children Hospital, 10126 Turin, Italy.
  • Saglio G; Department of Immunology, IRCCS Bambino Gesù Children's Hospital, 00165 Rome, Italy.
  • Verri A; Department of Clinical and Biological Sciences, University of Turin, 10043 Turin, Italy.
  • Barla A; Department of Informatics, Bioengineering, Robotics and Systems Engineering, University of Genoa, via Dodecaneso 35, 16146 Genoa, Italy.
  • Locatelli F; Department of Informatics, Bioengineering, Robotics and Systems Engineering, University of Genoa, via Dodecaneso 35, 16146 Genoa, Italy.
  • Frassoni F; Department of Pediatric Hematology and Oncology IRCCS; Ospedale Pediatrico Bambino Gesù, Rome, University of Pavia, 27100 Pavia, Italy.
J Clin Med ; 9(6)2020 Jun 01.
Article em En | MEDLINE | ID: mdl-32492887
ABSTRACT
During the phase of proliferation needed for hematopoietic reconstitution following transplantation, hematopoietic stem/progenitor cells (HSPC) must express genes involved in stem cell self-renewal. We investigated the expression of genes relevant for self-renewal and expansion of HSPC (operationally defined as CD34+ cells) in steady state and after transplantation. Specifically, we evaluated the expression of ninety-one genes that were analyzed by real-time PCR in CD34+ cells isolated from (i) 12 samples from umbilical cord blood (UCB); (ii) 15 samples from bone marrow healthy donors; (iii) 13 samples from bone marrow after umbilical cord blood transplant (UCBT); and (iv) 29 samples from patients after transplantation with adult hematopoietic cells. The results show that transplanted CD34+ cells from adult cells acquire an asset very different from transplanted CD34+ cells from cord blood. Multivariate machine learning analysis (MMLA) showed that four specific gene signatures can be obtained by comparing the four types of CD34+ cells. In several, but not all cases, transplanted HSPC from UCB overexpress reprogramming genes. However, these remarkable changes do not alter the commitment to hematopoietic lineage. Overall, these results reveal undisclosed aspects of transplantation biology.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: J Clin Med Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: J Clin Med Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Itália