• No results found

Towards adipose tissue-derived stromal cells-based therapy for diabetic retinopathy

N/A
N/A
Protected

Academic year: 2021

Share "Towards adipose tissue-derived stromal cells-based therapy for diabetic retinopathy"

Copied!
2
0
0

Bezig met laden.... (Bekijk nu de volledige tekst)

Hele tekst

(1)

University of Groningen

Towards adipose tissue-derived stromal cells-based therapy for diabetic retinopathy

Hajmousa, Ghazaleh

IMPORTANT NOTE: You are advised to consult the publisher's version (publisher's PDF) if you wish to cite from it. Please check the document version below.

Document Version

Publisher's PDF, also known as Version of record

Publication date: 2018

Link to publication in University of Groningen/UMCG research database

Citation for published version (APA):

Hajmousa, G. (2018). Towards adipose tissue-derived stromal cells-based therapy for diabetic retinopathy. University of Groningen.

Copyright

Other than for strictly personal use, it is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license (like Creative Commons).

Take-down policy

If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim.

Downloaded from the University of Groningen/UMCG research database (Pure): http://www.rug.nl/research/portal. For technical reasons the number of authors shown on this cover page is limited to 10 maximum.

(2)

Towards adipose tissue-derived stromal cells-based therapy for diabetic retinopathy

Propositions:

1. Adipose tissue derived stromal cells (ASC) support newly formed vascular

networks by endothelial cells (EC) in vitro and in vivo through maintenance of the vascular architecture (this thesis).

2. Administered ASC to the murine model of diabetic retinopathy augment

and stabilize retinal angiogenesis and co-localize with capillaries at a pericyte-specific position (this thesis).

3. The ROS-induced mitochondrial dysfunction, hyperglycemia-induced

apoptosis, and bioenergetics changes only partially influence the pericytic ability of ASC (this thesis).

4. Despite of the diminished level of glycolysis, ASC under HG showed the

same basal respiration as under NG which proves that ASC resist the HG condition by changing the metabolic limit deprived of altering the proliferation rate (this thesis).

5. Conditioned medium of ASC alleviates high glucose-induced oxidative

stress and its subsequent upregulated downstream targets in an NF-κB dependent fashion in bovine retinal endothelial cells (this thesis).

6. The manner of high glucose preconditioning of adipose tissue-derived

stromal cells dictates their immuno-regulatory properties (this thesis).

7. The antioxidant capacity of ASC-Cme downmodulates upregulated

pro-inflammatory genes in high glucose-challenged BREC (this thesis).

8. The new pharmacologic compound,

(6-hydroxyl-2,5,7,8-tetramethylchroman-2-yl)(4-(2-hydroxyethyl)piperazin-1-yl) methanone (SUL-109) shields ASC during cell preservation from hypothermic cell death without

Referenties

GERELATEERDE DOCUMENTEN

The observed differences in the prevalence of types of urinary incontinence between different race groups, and the association between muscle activity and pelvic floor

It is shown that the surface segregation behaviour in atomically clean Pt-Rh alloys can be understood quantitatively by taking into account the difference in

At sufficient rpm of the rotor the water stream closes the valve by the under pressure caused by the water acceleration through the slit between piston valve

Decoding therapeutic roles of adipose tissue-derived stromal cells and their extracellular vesicles in liver disease..

The overall aim of this thesis is to investigate the therapeutic potential of extracellular vesicles from human adipose-derived stromal cells (hASC-derived EVs) in the treatment

have been applied to analyze drug metabolism 37 and served as models of drug- induced cholestatic 38 , metabolic 39 , and fibrotic 35 liver disease, but this is the first-

IFATS collection: In vivo therapeutic potential of human adipose tissue mesenchymal stem cells after transplantation into mice with liver injury.. Kapur SK,

Here, we studied the prophylactic and therapeutic potential of hASC-derived extracellular vesicles (EVs) to attenuate the acute liver damage in APAP- and CCl 4 -induced murine