The Matricellular Protein R-Spondin 2 Promotes Midbrain Dopaminergic Neurogenesis and Differentiation

Gyllborg, Daniel, Ahmed, Maqsood, Toledo, Enrique M., Theofilopoulos, Spyridon, Yang, Shanzheng, ffrench-Constant, Charles ORCID: https://orcid.org/0000-0002-5621-3377 and Arenas, Ernest (2018) The Matricellular Protein R-Spondin 2 Promotes Midbrain Dopaminergic Neurogenesis and Differentiation. Stem Cell Reports, 11 (3). pp. 651-664. ISSN 2213-6711

Full text not available from this repository. (Request a copy)

Abstract

The development of midbrain dopaminergic (mDA) neurons is controlled by multiple morphogens and transcription factors. However, little is known about the role of extracellular matrix proteins in this process. Here we examined the function of roof plate-specific spondins (RSPO1-4) and the floor plate-specific, spondin 1 (SPON1). Only RSPO2 and SPON1 were expressed at high levels during mDA neurogenesis, and the receptor LGR5 was expressed by midbrain floor plate progenitors. Surprisingly, RSPO2, but not SPON1, specifically promoted the differentiation of mDA neuroblasts into mDA neurons in mouse primary cultures and embryonic stem cells (ESCs). In addition, RSPO2 was found to promote not only mDA differentiation, but also mDA neurogenesis in human ESCs. Our results thus uncover an unexpected function of the matricellular protein RSPO2 and suggest an application to improve mDA neurogenesis and differentiation in human stem cell preparations destined to cell replacement therapy or drug discovery for Parkinson disease. Gyllborg and colleagues report on the function of the matricellular protein R-Spondin 2 (RSPO2) in dopaminergic neuron development. RSPO2 is dynamically expressed during midbrain development and promotes the dopaminergic differentiation of mouse and human neuroblasts. Furthermore, they show that RSPO2 induced dopaminergic neurogenesis in human stem cell cultures, suggesting a possible application of RSPO2 in cell replacement strategies for Parkinson disease.

Item Type: Article
Additional Information: Funding Information: We thank Linda Adlerz for her support with the qPCR experiments, members of the Arenas lab for their help and suggestions, and Alessandra Nanni for technical and secretarial assistance. Financial support was obtained from Swedish Research Council (VR projects: DBRM, 2011-3116, 2011-3318, and 2016-01526), Swedish Foundation for Strategic Research (SRL and SB16-0065), European Commission (NeuroStemCellRepair and DDPD-Genes), Karolinska Institutet, Hjärnfonden (FO2015:0202, FO2017:0059), Cancerfonden (CAN 2016/572), and SFO Strat Regen (SG-2018) to E.A. E.M.T. received a fellowship from VR. M.A. and C. ffrench-Constant were supported by NeuroStemCellRepair and Wellcome Trust Senior Investigator Award. Funding Information: We thank Linda Adlerz for her support with the qPCR experiments, members of the Arenas lab for their help and suggestions, and Alessandra Nanni for technical and secretarial assistance. Financial support was obtained from Swedish Research Council (VR projects: DBRM, 2011-3116 , 2011-3318 , and 2016-01526 ), Swedish Foundation for Strategic Research (SRL and SB16-0065 ), European Commission (NeuroStemCellRepair and DDPD-Genes), Karolinska Institutet , Hjärnfonden ( FO2015:0202 , FO2017:0059 ), Cancerfonden (CAN 2016/572 ), and SFO Strat Regen ( SG-2018 ) to E.A. E.M.T. received a fellowship from VR. M.A. and C. ffrench-Constant were supported by NeuroStemCellRepair and Wellcome Trust Senior Investigator Award.
Uncontrolled Keywords: cell replacement,differentiation,dopaminergic neurons,extracellular matrix,human embryonic stem cells,neurogenesis,parkinson disease,progenitors,rspo2,wnt,biochemistry,genetics,developmental biology,cell biology,sdg 3 - good health and well-being ,/dk/atira/pure/subjectarea/asjc/1300/1303
Faculty \ School: Faculty of Medicine and Health Sciences > Norwich Medical School
Related URLs:
Depositing User: LivePure Connector
Date Deposited: 15 Jul 2022 14:31
Last Modified: 12 Aug 2022 05:37
URI: https://ueaeprints.uea.ac.uk/id/eprint/86232
DOI: 10.1016/j.stemcr.2018.07.014

Actions (login required)

View Item View Item