Articles producció científicaMedicina i Cirurgia

A Glycovariant of Human CD44 Is Characteristically Expressed on Human Mesenchymal Stem Cells

  • Datos identificativos

    Identificador:  imarina:5131209
    Autores:  Pachon-Pena, Gisela; Donnelly, Conor; Ruiz-Canada, Catalina; Katz, Adam; Fernandez-Veledo, Sonia; Vendrell, Joan; Sackstein, Robert
    Resumen:
    The clinical effectiveness of systemically administered human mesenchymal stem cells (hMSCs) depends on their capacity to engage vascular endothelium. hMSCs derived from bone marrow (BM-hMSCs) natively lack endothelial binding capacity, but express a CD44 glycovariant containing N-linked sialyllactosamines that can be α(1,3)-fucosylated using fucosyltransferase-VI (FTVI) to enforce sLeX decorations, thereby creating hematopoietic cell E-/L-selectin ligand (HCELL). HCELL expression programs potent shear-resistant adhesion of circulating cells to endothelial beds expressing E-selectin. An alternative source of hMSCs is adipose tissue (A-hMSCs), and we assessed whether A-hMSCs bind E-selectin and/or possess sialyllactosamine-decorated CD44 accessible to α(1,3)-fucosylation. Similar to BM-hMSCs, we found that A-hMSCs natively lack E-selectin ligands, but FTVI-mediated cell surface α(1,3)-fucosylation induces sLeX expression and robust E-selectin binding secondary to conversion of CD44 into HCELL. Moreover, treatment with the α(1,3)-fucosyltransferase-FTVII also generated expression of HCELL on both BM-hMSCs and A-hMSCs, with sLeX decorations created on N-linked glycans of the 'standard' CD44 (CD44s) isoform. The finding that hMSCs from both source tissues each lack native E-selectin ligand expression prompted examination of the expression of glycosyltransferases that direct lactosaminyl glycan synthesis. These studies reveal that both types of hMSCs conspicuously lack transcripts encoding α(1,3)-fucosyltransferases, but equally express glycosyltransferases critical to creation of sialyllactosamines. Collectively, these data indicate that assembly of a sialyllactosaminyl-decorated CD44s glycovariant is a conserved feature of hMSCs derived from adipose tissue and marrow, thus
  • Otros:

    Autor según el artículo: Pachon-Pena, Gisela; Donnelly, Conor; Ruiz-Canada, Catalina; Katz, Adam; Fernandez-Veledo, Sonia; Vendrell, Joan; Sackstein, Robert
    Departamento: Medicina i Cirurgia; Ciències Mèdiques Bàsiques
    Autor/es de la URV: Fernandez Veledo, Sonia / Vendrell Ortega, Juan José
    Palabras clave: Stromal cells; Slex; Sle(x); Sle x; Sialyl lewis x; Protein binding; Polysaccharides; Neuraminidase; Mesenchymal stem cells; Mesenchymal stem cell; Ligands; L-selectin; Immunophenotyping; Hyaluronan receptors; Humans; Hematopoietic cell e-/l-selectin ligand; Hematopoietic cell e-/ l-selectin ligand; Glycosyltransferases; Glycosyltransferase-programmed stereosubstitution; Glycosylation; Glycoproteins; Gene expression regulation; Fucosyltransferase; Fucosyl-transferases; Fibronectins; Exofucosylation; E-selectin ligands; E-selectin ligand; E-selectin; Cell line; Cell differentiation; Cell adhesion; Cd44 protein, human; Bone marrow cells; Adipose tissue; sialyl lewis x; mesenchymal stem cell; hematopoietic cell e-/l-selectin ligand; glycosyltransferase-programmed stereosubstitution; fucosyltransferase; exofucosylation; e-selectin ligand
    Resumen: The clinical effectiveness of systemically administered human mesenchymal stem cells (hMSCs) depends on their capacity to engage vascular endothelium. hMSCs derived from bone marrow (BM-hMSCs) natively lack endothelial binding capacity, but express a CD44 glycovariant containing N-linked sialyllactosamines that can be α(1,3)-fucosylated using fucosyltransferase-VI (FTVI) to enforce sLeX decorations, thereby creating hematopoietic cell E-/L-selectin ligand (HCELL). HCELL expression programs potent shear-resistant adhesion of circulating cells to endothelial beds expressing E-selectin. An alternative source of hMSCs is adipose tissue (A-hMSCs), and we assessed whether A-hMSCs bind E-selectin and/or possess sialyllactosamine-decorated CD44 accessible to α(1,3)-fucosylation. Similar to BM-hMSCs, we found that A-hMSCs natively lack E-selectin ligands, but FTVI-mediated cell surface α(1,3)-fucosylation induces sLeX expression and robust E-selectin binding secondary to conversion of CD44 into HCELL. Moreover, treatment with the α(1,3)-fucosyltransferase-FTVII also generated expression of HCELL on both BM-hMSCs and A-hMSCs, with sLeX decorations created on N-linked glycans of the 'standard' CD44 (CD44s) isoform. The finding that hMSCs from both source tissues each lack native E-selectin ligand expression prompted examination of the expression of glycosyltransferases that direct lactosaminyl glycan synthesis. These studies reveal that both types of hMSCs conspicuously lack transcripts encoding α(1,3)-fucosyltransferases, but equally express glycosyltransferases critical to creation of sialyllactosamines. Collectively, these data indicate that assembly of a sialyllactosaminyl-decorated CD44s glycovariant is a conserved feature of hMSCs derived from adipose tissue and marrow, thus identifying a CD44 glycosignature of these cells and supporting the applicability of cell surface α(1,3)-fucosylation in programming migration of systemically administered A-hMSCs to sites of tissue injury/inflammation. Stem Cells 2017;35:1080-1092.
    Áreas temáticas: Oncology; Nutrição; Molecular medicine; Medicine (miscellaneous); Medicine (all); Medicina veterinaria; Medicina ii; Medicina i; Interdisciplinar; Hematology; General medicine; Farmacia; Engenharias ii; Educação física; Developmental biology; Ciências biológicas iii; Ciências biológicas ii; Ciências biológicas i; Cell biology; Cell & tissue engineering; Biotecnología; Biotechnology & applied microbiology
    Acceso a la licencia de uso: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 15494918
    Direcció de correo del autor: sonia.fernandez@urv.cat; jvortega@iispv.cat
    Fecha de alta del registro: 2025-03-03
    Versión del articulo depositado: info:eu-repo/semantics/acceptedVersion
    Enlace a la fuente original: https://stemcellsjournals.onlinelibrary.wiley.com/doi/full/10.1002/stem.2549
    URL Documento de licencia: https://repositori.urv.cat/ca/proteccio-de-dades/
    Referencia al articulo segun fuente origial: Stem Cells. 35 (4): 1080-1092
    Referencia de l'ítem segons les normes APA: Pachon-Pena, Gisela; Donnelly, Conor; Ruiz-Canada, Catalina; Katz, Adam; Fernandez-Veledo, Sonia; Vendrell, Joan; Sackstein, Robert (2017). A Glycovariant of Human CD44 Is Characteristically Expressed on Human Mesenchymal Stem Cells. Stem Cells, 35(4), 1080-1092. DOI: 10.1002/stem.2549
    DOI del artículo: 10.1002/stem.2549
    Entidad: Universitat Rovira i Virgili
    Año de publicación de la revista: 2017
    Tipo de publicación: Journal Publications
  • Palabras clave:

    Biotechnology & Applied Microbiology,Cell & Tissue Engineering,Cell Biology,Developmental Biology,Hematology,Medicine (Miscellaneous),Molecular Medicine,Oncology
    Stromal cells
    Slex
    Sle(x)
    Sle x
    Sialyl lewis x
    Protein binding
    Polysaccharides
    Neuraminidase
    Mesenchymal stem cells
    Mesenchymal stem cell
    Ligands
    L-selectin
    Immunophenotyping
    Hyaluronan receptors
    Humans
    Hematopoietic cell e-/l-selectin ligand
    Hematopoietic cell e-/ l-selectin ligand
    Glycosyltransferases
    Glycosyltransferase-programmed stereosubstitution
    Glycosylation
    Glycoproteins
    Gene expression regulation
    Fucosyltransferase
    Fucosyl-transferases
    Fibronectins
    Exofucosylation
    E-selectin ligands
    E-selectin ligand
    E-selectin
    Cell line
    Cell differentiation
    Cell adhesion
    Cd44 protein, human
    Bone marrow cells
    Adipose tissue
    sialyl lewis x
    mesenchymal stem cell
    hematopoietic cell e-/l-selectin ligand
    glycosyltransferase-programmed stereosubstitution
    fucosyltransferase
    exofucosylation
    e-selectin ligand
    Oncology
    Nutrição
    Molecular medicine
    Medicine (miscellaneous)
    Medicine (all)
    Medicina veterinaria
    Medicina ii
    Medicina i
    Interdisciplinar
    Hematology
    General medicine
    Farmacia
    Engenharias ii
    Educação física
    Developmental biology
    Ciências biológicas iii
    Ciências biológicas ii
    Ciências biológicas i
    Cell biology
    Cell & tissue engineering
    Biotecnología
    Biotechnology & applied microbiology
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