• No results found

University of Groningen Sorting out cholesterol metabolism Wijers, Melinde

N/A
N/A
Protected

Academic year: 2021

Share "University of Groningen Sorting out cholesterol metabolism Wijers, Melinde"

Copied!
2
0
0

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

Hele tekst

(1)

University of Groningen

Sorting out cholesterol metabolism

Wijers, Melinde

DOI:

10.33612/diss.102035320

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: 2019

Link to publication in University of Groningen/UMCG research database

Citation for published version (APA):

Wijers, M. (2019). Sorting out cholesterol metabolism: novel insights into the mechanism of endosomal trafficking of lipoprotein receptors. Rijksuniversiteit Groningen. https://doi.org/10.33612/diss.102035320

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)

Propositions belonging to the PhD thesis

Sorting out cholesterol metabolism: Novel insights into the mechanism

of endosomal trafficking of lipoprotein receptors

1. To understand the complexity of the endosomal sorting machinery requires the complexity of an in vivo model – This thesis

2. Components of the endosomal sorting machinery act in various compositions, enabling the fine-tuning of biological processes, including lipid metabolism – This thesis

3. Individuals with superior endocytic recycling might have lower cardiovascular risk due to improved plasma LDL cholesterol clearance – This thesis

4. Proper lysosomal architecture is not requisite to maintain intracellular cholesterol transport – This thesis

5. Somatic gene editing technology is a versatile and powerful tool to decipher the molecular organization and the physiological role of the endosomal sorting machinery, allowing us to bring research on the endo-lysosomal system to the next level- This thesis

6. Upon suppression or ablation of retromer, retriever, the WASH complex, or the CCC complex, cargos are degraded in lysosomes, suggesting that cargo degradation may be the default pathway –James McNally, trends in biology 7. Our understanding of endosomal sorting has been restricted by a tendency to focus on individual model cargos, and the isolated characterization of protein complexes that define individual sorting events - Peter J Cullen 8. Progress in science depends on new techniques, new discoveries and new

ideas, probably in that order – Sydney Brenner

9. If we will only allow that, as we progress, we remain unsure, we will leave opportunities for alternatives – Richard Feynman

Referenties

GERELATEERDE DOCUMENTEN

Based on this warehouse we create different settings by varying the fraction of singles in each order, the number of orders, the sorting speed of non-clean compartments, the number

In addition, LRP1 controls cellular cholesterol efflux by modulating the expression of ABCA1 and ABCG1, and hepatic LRP1 protects against diet-induced hepatic insulin

Although the total protein levels of hepatic LDLR and LRP1 in WT and ApoE3*L mice are not affected upon CCC inactivation, this study and our previous work (8) showed that

Hepatic WASH/LDLR deficiency mimics the plasma lipid phenotype in hepatic LRP1-deficient mice with an Ldlr knockout background (27), suggesting that the WASH complex is also

Cyp7a1 catalyzes the first and rate-limiting step in the conversion of cholesterol into bile acids in mice (30); however, decreased Cyp7a1 expression in Washc1 depleted

tail of LDLR or LRP1 and, together with DSCR3/VPS35C, retrieves the receptors from lysosomal degradation after endocytosis. The WASH complex is recruited to the endosomes, which

We focused specifically on the contribution of the endosomal network to cholesterol metabolism and atherosclerosis by studying the molecular regulation of the

tail of LDLR or LRP1 and, together with DSCR3/VPS35C, retrieves the receptors from lysosomal degradation after endocytosis. The WASH complex is recruited to the endosomes, which