BACKGROUND AIMS: Mesenchymal stromal cells (MSC) exhibit non-specific hematopoietic cell and/or stromal cell markers (e.g. CD73, CD105 and CD166) that have been used to identify MSC by flow cytometry. Because a neural glial antigen, NG2 (a progenitor cell marker in the central nervous system), is expressed by several tissue cells originating in the mesenchyme but not hematopoietic cells, it might be useful for isolating and identifying MSC. We investigated NG2 expression on culture-expanded MSC by flow cytometry. METHODS: Human bone marrow (BM) samples taken from 12 donors were cultured for MSC to be used in up to nine serial passages. Using flow cytometry, the neural glial antigen NG2 and commonly used MSC markers CD73, CD105 and CD166, were analyzed on the surface of culture-expanded MSC. The multipotential differentiation of the MSC was examined by adipogenic and osteogenic induction. RESULTS: The percentage of cells positive for NG2 was similar to the percentages of cells positive for CD73, CD105 and CD166 in all passages of BM samples. The mean fluorescent intensities of NG2 did not change with culture passage. The MSC was successfully differentiated into adipogenic and osteogenic lines. The cells showed no karyotypic abnormalities. CONCLUSIONS: NG2 seems to be a promising marker for investigating the biology of MSC.
BACKGROUND AIMS: Mesenchymal stromal cells (MSC) exhibit non-specific hematopoietic cell and/or stromal cell markers (e.g. CD73, CD105 and CD166) that have been used to identify MSC by flow cytometry. Because a neural glial antigen, NG2 (a progenitor cell marker in the central nervous system), is expressed by several tissue cells originating in the mesenchyme but not hematopoietic cells, it might be useful for isolating and identifying MSC. We investigated NG2 expression on culture-expanded MSC by flow cytometry. METHODS:Human bone marrow (BM) samples taken from 12 donors were cultured for MSC to be used in up to nine serial passages. Using flow cytometry, the neural glial antigen NG2 and commonly used MSC markers CD73, CD105 and CD166, were analyzed on the surface of culture-expanded MSC. The multipotential differentiation of the MSC was examined by adipogenic and osteogenic induction. RESULTS: The percentage of cells positive for NG2 was similar to the percentages of cells positive for CD73, CD105 and CD166 in all passages of BM samples. The mean fluorescent intensities of NG2 did not change with culture passage. The MSC was successfully differentiated into adipogenic and osteogenic lines. The cells showed no karyotypic abnormalities. CONCLUSIONS:NG2 seems to be a promising marker for investigating the biology of MSC.
Authors: Matthew A Price; Leah E Colvin Wanshura; Jianbo Yang; Jennifer Carlson; Bo Xiang; Guiyuan Li; Soldano Ferrone; Arkadiusz Z Dudek; Eva A Turley; James B McCarthy Journal: Pigment Cell Melanoma Res Date: 2011-12 Impact factor: 4.693
Authors: Heike Wegmeyer; Ann-Marie Bröske; Mathias Leddin; Karin Kuentzer; Anna Katharina Nisslbeck; Julia Hupfeld; Kornelius Wiechmann; Jennifer Kuhlen; Christoffer von Schwerin; Carsten Stein; Saskia Knothe; Jürgen Funk; Ralf Huss; Markus Neubauer Journal: Stem Cells Dev Date: 2013-06-22 Impact factor: 3.272
Authors: Troy C Lund; Xiaobai Patrinostro; Ashley C Kramer; Paul Stadem; Lee Ann Higgins; Todd W Markowski; Matt S Wroblewski; Diane S Lidke; Jakub Tolar; Bruce R Blazar Journal: Stem Cells Date: 2014-10 Impact factor: 6.277
Authors: Andrew K Edwards; Kyle Glithero; Peter Grzesik; Alison A Kitajewski; Naikhoba Co Munabi; Krista Hardy; Qian Kun Tan; Michael Schonning; Thaned Kangsamaksin; Jan K Kitajewski; Carrie J Shawber; June K Wu Journal: JCI Insight Date: 2017-11-02
Authors: Katie C Russell; H Alan Tucker; Bruce A Bunnell; Michael Andreeff; Wendy Schober; Andrew S Gaynor; Karen L Strickler; Shuwen Lin; Michelle R Lacey; Kim C O'Connor Journal: Tissue Eng Part A Date: 2013-05-30 Impact factor: 3.845
Authors: June K Wu; Christopher Kitajewski; Maia Reiley; Connie H Keung; Julie Monteagudo; John P Andrews; Peter Liou; Arul Thirumoorthi; Alvin Wong; Jessica J Kandel; Carrie J Shawber Journal: PLoS One Date: 2015-02-26 Impact factor: 3.240