Detailed Information on Publication Record
2021
Targeted mass spectrometry for monitoring of neural differentiation
SUCHA, Rita, Martina KUBICKOVA, Jakub CERVENKA, Marian HRUSKA-PLOCHAN, Dáša BOHAČIAKOVÁ et. al.Basic information
Original name
Targeted mass spectrometry for monitoring of neural differentiation
Authors
SUCHA, Rita (203 Czech Republic), Martina KUBICKOVA (203 Czech Republic), Jakub CERVENKA (203 Czech Republic), Marian HRUSKA-PLOCHAN, Dáša BOHAČIAKOVÁ (703 Slovakia, belonging to the institution), Katerina KEPKOVA VODICKOVA (203 Czech Republic), Tereza NOVAKOVA (203 Czech Republic), Katerina BUDKOVA (203 Czech Republic), Andrej SUSOR, Martin MARSALA (203 Czech Republic), Jan MOTLIK (203 Czech Republic), Hana KOVAROVA (203 Czech Republic) and Petr VODICKA (203 Czech Republic, guarantor)
Edition
Biology Open, CAMBRIDGE, COMPANY BIOLOGISTS LTD, 2021, 2046-6390
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10602 Biology , Evolutionary biology
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 2.643
RIV identification code
RIV/00216224:14110/21:00119648
Organization unit
Faculty of Medicine
UT WoS
000692170900005
Keywords in English
Neural stem cell; Neural differentiation; Selected reaction monitoring; Mass spectrometry; Cell line characterization; Protein marker
Tags
International impact, Reviewed
Změněno: 15/2/2022 09:15, Mgr. Tereza Miškechová
Abstract
V originále
Human multipotent neural stem cells could effectively be used for the treatment of a variety of neurological disorders. However, a defining signature of neural stem cell lines that would be expandable, non-tumorigenic, and differentiate into desirable neuronal/glial phenotype after in vivo grafting is not yet defined. Employing a mass spectrometry approach, based on selected reaction monitoring, we tested a panel of well-described culture conditions, and measured levels of protein markers routinely used to probe neural differentiation, i.e. POU5F1 (OCT4), SOX2, NES, DCX, TUBB3, MAP2, S100B, GFAP, GALC, and OLIG1. Our multiplexed assay enabled us to simultaneously identify the presence of pluripotent, multipotent, and lineage committed neural cells, thus representing a powerful tool to optimize novel and highly specific propagation and differentiation protocols. The multiplexing capacity of this method permits the addition of other newly identified cell type-specific markers to further increase the specificity and quantitative accuracy in detecting targeted cell populations. Such an expandable assay may gain the advantage over traditional antibody-based assays, and represents a method of choice for quality control of neural stem cell lines intended for clinical use.
Links
GJ15-18316Y, research and development project |
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