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Proteome analysis of conditioned medium from cultured adult hippocampal progenitors
Author(s) -
Dahl Annika,
Eriksson Peter S,
Persson Anders I,
Karlsson Gosta,
Davidsson Pia,
Ekman Rolf,
WestmanBrinkmalm Ann
Publication year - 2003
Publication title -
rapid communications in mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.528
H-Index - 136
eISSN - 1097-0231
pISSN - 0951-4198
DOI - 10.1002/rcm.1183
Subject(s) - chemistry , proteome , hippocampal formation , progenitor cell , microbiology and biotechnology , biochemistry , neuroscience , stem cell , biology
It is known that proliferation and survival of neural stem/progenitor cells in vitro not only depend on exogenous factors, but also on autocrine factors secreted into the conditioned medium. It is also well known that the identification of bioactive proteins secreted into the conditioned medium poses a substantial challenge. Recently, neural stem/progenitor cells were shown to secrete a survival factor, cystatin C, into the conditioned medium. Here, we demonstrate an approach to identify other low molecular weight proteins in conditioned medium from cultured adult rat hippocampal progenitor cells. A combination of preparative two‐dimensional gel electrophoresis (2‐DE) and mass spectrometry was utilized in the analysis. We were able to identify a number of proteins, which include Rho‐guanine nucleotide dissociation inhibitor 1, phosphatidylethanolamine binding protein (PEBP), also termed Raf‐1 kinase interacting protein, polyubiquitin, immunophilin FK506 binding protein 12 (FKBP12) and cystatin C. The presence of PEBP and FKBP12 in conditioned medium was confirmed immunologically. All nestin‐positive progenitor cells showed immunoreactivity for antibodies against PEBP and FKBP12. To our knowledge we are the first to use this preparative proteomic approach to search for stem cell factors in conditioned medium. The method could be used to identify novel bioactive proteins secreted by stem/progenitor cells in vitro . Identification of bioactive proteins in vitro is of potential importance for the understanding of the regulatory mechanisms of the cells in vivo . Copyright © 2003 John Wiley & Sons, Ltd.