Progress in human pluripotent stem cell-based modeling systems
for neurological diseases

J 2017

Progress in human pluripotent stem cell-based modeling systems for neurological diseases

HŘÍBKOVÁ, Hana, Jana ZELINKOVÁ and Yuh-Man WADELEY

Basic information

Original name

Progress in human pluripotent stem cell-based modeling systems for neurological diseases

Authors

HŘÍBKOVÁ, Hana (203 Czech Republic, belonging to the institution), Jana ZELINKOVÁ (203 Czech Republic, belonging to the institution) and Yuh-Man WADELEY (826 United Kingdom of Great Britain and Northern Ireland, guarantor, belonging to the institution)

Edition

Neurogenesis, Oxford, Taylor & Francis, 2017, 2326-2133

Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

10600 1.6 Biological sciences

Country of publisher

United Kingdom of Great Britain and Northern Ireland

Confidentiality degree

není předmětem státního či obchodního tajemství

RIV identification code

RIV/00216224:14110/17:00098812

Organization unit

Faculty of Medicine

DOI

http://dx.doi.org/10.1080/23262133.2017.1324258

Keywords in English

3-D culturing; cell fate decision; hPSC-based disease modeling; human pluripotent stem cell; neural developmental modeling

Abstract

V originále

Human pluripotent stem cell (hPSC)-based modeling offers the potential for studying human diseases using human systems. An increasing number of studies in numerous fields demonstrate that hPSC-based disease systems capture disease specific pathophysiology occurring in vivo. A widespread deployment of hPSC systems is foreseeable. Even the field of psychiatric disorders (for example, schizophrenia and autism), which lags behind due to complex underlying causes, such as the inaccessibility of brain cells for assessments and the absence of reliable models, has been embracing the hPSC-based disease system. However, despite hPSCs holding great potential, it is imperative to validate how faithful hPSC-based neural developmental modeling is in recapitulating the developmental process in vivo. Our recent study demonstrated that the hPSC-based system mimicked the process of neural development and the system reserved neural stem cell (NSC) niches similar to those residing in the ventricular region of the cortex. In this article, we will first comment on an array of factors that affect hPSC-based neural differentiation and summarize the intricate regulatory signaling pathways that regionalize neuronal cell types. Finally, we review successful studies in brain-related diseases using hPSC-based modeling with 3-D systems.

Citovat

HŘÍBKOVÁ, Hana, Jana ZELINKOVÁ and Yuh-Man WADELEY. Progress in human pluripotent stem cell-based modeling systems for neurological diseases. Neurogenesis. Oxford: Taylor & Francis, 2017, vol. 4, No 1, p. "e1324258-1"-"e1324258-6", 6 pp. ISSN 2326-2133. Available from: https://dx.doi.org/10.1080/23262133.2017.1324258.

@article{1399292,
   author = {Hříbková, Hana and Zelinková, Jana and Wadeley, YuhandMan},
   article_location = {Oxford},
   article_number = {1},
   doi = {http://dx.doi.org/10.1080/23262133.2017.1324258},
   keywords = {3-D culturing; cell fate decision; hPSC-based disease modeling; human pluripotent stem cell; neural developmental modeling},
   language = {eng},
   issn = {2326-2133},
   journal = {Neurogenesis},
   title = {Progress in human pluripotent stem cell-based modeling systems for neurological diseases},
   volume = {4},
   year = {2017}
}

TY  - JOUR
ID  - 1399292
AU  - Hříbková, Hana - Zelinková, Jana - Wadeley, Yuh-Man
PY  - 2017
TI  - Progress in human pluripotent stem cell-based modeling systems for neurological diseases
JF  - Neurogenesis
VL  - 4
IS  - 1
SP  - "e1324258-1"-"e1324258-6"
EP  - "e1324258-1"-"e1324258-6"
PB  - Taylor & Francis
SN  - 23262133
KW  - 3-D culturing
KW  - cell fate decision
KW  - hPSC-based disease modeling
KW  - human pluripotent stem cell
KW  - neural developmental modeling
N2  - Human pluripotent stem cell (hPSC)-based modeling offers the potential for studying human diseases using human systems. An increasing number of studies in numerous fields demonstrate that hPSC-based disease systems capture disease specific pathophysiology occurring in vivo. A widespread deployment of hPSC systems is foreseeable. Even the field of psychiatric disorders (for example, schizophrenia and autism), which lags behind due to complex underlying causes, such as the inaccessibility of brain cells for assessments and the absence of reliable models, has been embracing the hPSC-based disease system. However, despite hPSCs holding great potential, it is imperative to validate how faithful hPSC-based neural developmental modeling is in recapitulating the developmental process in vivo. Our recent study demonstrated that the hPSC-based system mimicked the process of neural development and the system reserved neural stem cell (NSC) niches similar to those residing in the ventricular region of the cortex. In this article, we will first comment on an array of factors that affect hPSC-based neural differentiation and summarize the intricate regulatory signaling pathways that regionalize neuronal cell types. Finally, we review successful studies in brain-related diseases using hPSC-based modeling with 3-D systems.
ER  -

HŘÍBKOVÁ, Hana, Jana ZELINKOVÁ and Yuh-Man WADELEY. Progress in human pluripotent stem cell-based modeling systems for neurological diseases. \textit{Neurogenesis}. Oxford: Taylor \&{} Francis, 2017, vol.~4, No~1, p.~''e1324258-1''-''e1324258-6'', 6 pp. ISSN~2326-2133. Available from: https://dx.doi.org/10.1080/23262133.2017.1324258.

Detailed Information on Publication Record