J 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

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
Name: Úloha microRNA v řízení buněčného dělení a diferenciace lidských embryonálních kmenových buněk do neurálních kmenových buněk. (Acronym: miRNA v diferenciaci lidských EK buněk)
Investor: Czech Science Foundation