Digital repository of Slovenian research organisations

Show document
A+ | A- | Help | SLO | ENG

Title:Transcriptomic and proteomic profiling of bi-partite and tri-partite murine iPSC-derived neurospheroids under steady-state and inflammatory condition
Authors:ID Di Stefano, Julia (Author)
ID Garcia-Pupo, Laura (Author)
ID Motaln, Helena, Institut "Jožef Stefan" (Author)
ID Rogelj, Boris (Author)
ID Ponsaerts, Peter (Author)
Files:URL URL - Source URL, visit https://www.sciencedirect.com/science/article/pii/S0889159124004756?via%3Dihub
 
.pdf PDF - Presentation file, download (9,35 MB)
MD5: BB60590C9445DC51CC8735372AAB1566
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo IJS - Jožef Stefan Institute
Abstract:Induced-pluripotent stem cell (iPSC)-derived neurospheroid (NSPH) models are an emerging in vitro toolkit to study the influence of inflammatory triggers on neurodegeneration and repair in a 3D neural environment. In contrast to their human counterpart, the absence of murine iPSC-derived NSPHs for profound characterisation and validation studies is a major experimental research gap, even though they offer the only possibility to truly compare or validate in vitro NSPH responses with in vivo brain responses. To contribute to these developments, we here describe the generation and characterisation of 5-week-old CX3CR1eGFP+/- CCR2RFP+/- murine (m)iPSC-derived bi-partite (neurons + astrocytes) and tri-partite (neurons + astrocytes + microglia) NSPH models that can be subjected to cellular activation following pro-inflammatory stimulation. First, cytokine analysis demonstrates that both bi-partite and tri-partite NSPHs can be triggered to release IL6 and CXCL10 following three days of stimulation with, respectively, TNFα + IL1β + IFNγ and LPS + IFNγ. Additionally, immunocytochemical analysis for G3BP1 and PABPC1 revealed the development of stress granules in both bi-partite and tri-partite NSPHs after 3 days of stimulation. To further investigate the observed signs of inflammatory response and cellular stress, we performed an untargeted transcriptomic and proteomic analysis of bi- and tri-partite NSPHs under steady-state and inflammatory conditions. Here, using the combined differential gene and protein expression profiles between unstimulated and stimulated NSPHs, Ingenuity Pathway Analysis (IPA) confirms the activation of canonical pathways associated with inflammation and cellular stress in both bi-partite and tri-partite NSPHs. Moreover, our multi-omics analysis suggests a higher level of downstream inflammatory responses, impairment of homeostatic and developmental processes, as well as activation of cell death processes in stimulated tri-partite NSPHs compared to bi-partite NSPHs. Concluding, these results emphasise the advantages of including microglia in NSPH research to study inflammation-induced neurodegeneration in a 3D neural environment.
Keywords:murine induced-pluripotent cells, neurospheroids, inflammatory response, stress granules, transcriptomics, proteomics
Submitted for review:24.05.2024
Article acceptance date:06.07.2024
Publication date:14.07.2024
Publisher:Elsevier
Year of publishing:2024
Number of pages:str. 1-12
Numbering:Vol. 121
Source:Nizozemska
PID:20.500.12556/DiRROS-21158 New window
UDC:57
ISSN on article:1090-2139
DOI:10.1016/j.bbi.2024.07.008 New window
COBISS.SI-ID:206077443 New window
Copyright:© 2024 Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
Note:Nasl. z nasl. zaslona; Soavtorja iz Slovenije: Helena Motaln, Boris Rogelj; Opis vira z dne 2. 9. 2024;
Publication date in DiRROS:08.01.2025
Views:31
Downloads:9
Metadata:XML DC-XML DC-RDF
:
Copy citation
  
Share:Bookmark and Share


Hover the mouse pointer over a document title to show the abstract or click on the title to get all document metadata.

Record is a part of a journal

Title:Brain, behavior, and immunity
Shortened title:Brain behav. immun.
Publisher:Academic Press
ISSN:1090-2139
COBISS.SI-ID:206074371 New window

Document is financed by a project

Funder:Other - Other funder or multiple funders
Project number:813263

Funder:Other - Other funder or multiple funders
Project number:G091518N

Funder:Other - Other funder or multiple funders
Project number:K800224N

Funder:Other - Other funder or multiple funders
Project number:V511123N

Funder:Other - Other funder or multiple funders
Project number:I003420N

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P4-0127
Name:Farmacevtska biotehnologija: znanost za zdravje

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:J3-3065
Name:Ciljanje faznega ločevanja in agregacije proteinov v nevrodegenerativnih proteinopatijah TDP-43

Funder:Other - Other funder or multiple funders
Project number:47375 TRANS4AD

Funder:Other - Other funder or multiple funders
Project number:20230041

Funder:Other - Other funder or multiple funders
Project number:BOF-SEP 2022

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:14.07.2024
Applies to:VoR

Secondary language

Language:Slovenian
Keywords:vnetni odziv, proteomika


Back