Mammalian pexophagy at a glance DOI Creative Commons

Justyna Bajdzienko,

Anja Bremm

Journal of Cell Science, Год журнала: 2024, Номер 137(9)

Опубликована: Май 1, 2024

ABSTRACT Peroxisomes are highly plastic organelles that involved in several metabolic processes, including fatty acid oxidation, ether lipid synthesis and redox homeostasis. Their abundance activity dynamically regulated response to nutrient availability cellular stress. Damaged or superfluous peroxisomes removed mainly by pexophagy, the selective autophagy of induced ubiquitylation peroxisomal membrane proteins ubiquitin-independent processes. Dysregulated pexophagy impairs peroxisome homeostasis has been linked development various human diseases. Despite many recent insights into mammalian our understanding this process is still limited compared yeast. In Cell Science at a Glance article accompanying poster, we summarize current knowledge on control highlight which aspects require further attention. We also discuss role describe ubiquitin machinery regulating signals for recruitment phagophores peroxisomes.

Язык: Английский

A genome-wide screen links peroxisome regulation with Wnt signaling through RNF146 and TNKS/2 DOI Creative Commons
Jonathan T. Vu, Katherine U. Tavasoli, Connor J. Sheedy

и другие.

The Journal of Cell Biology, Год журнала: 2024, Номер 223(10)

Опубликована: Июль 5, 2024

Peroxisomes are membrane-bound organelles harboring metabolic enzymes. In humans, peroxisomes required for normal development, yet the genes regulating peroxisome function remain unclear. We performed a genome-wide CRISPRi screen to identify novel factors involved in peroxisomal homeostasis. found that inhibition of RNF146, an E3 ligase activated by poly(ADP-ribose), reduced import proteins into peroxisomes. RNF146-mediated loss depended on stabilization and activity poly(ADP-ribose) polymerases TNKS TNKS2, which bind membrane protein PEX14. propose RNF146 TNKS/2 regulate efficiency PARsylation at membrane. Interestingly, we increased RNF146-dependent degradation non-peroxisomal substrates, including β-catenin destruction complex component AXIN1, was sufficient alter amplitude transcription. Together, these observations not only suggest previously undescribed roles regulation but also role bridging with Wnt/β-catenin signaling during development.

Язык: Английский

Процитировано

5

Mitochondrial regulation of erythropoiesis in homeostasis and disease DOI
Vijay Menon,

Mary Slavinsky,

Olivier Hermine

и другие.

British Journal of Haematology, Год журнала: 2024, Номер 205(2), С. 429 - 439

Опубликована: Июнь 30, 2024

Summary Erythroid cells undergo a highly complex maturation process, resulting in dynamic changes that generate red blood (RBCs) rich haemoglobin. The end stages of the erythroid cell process primarily include chromatin condensation and nuclear polarization, followed by expulsion called enucleation clearance mitochondria other organelles to finally mature RBCs. While healthy RBCs are devoid mitochondria, recent evidence suggests actively implicated processes maturation, erythroblast RBC production. However, extent mitochondrial participation occurs during these ultimate steps is not completely understood. This specifically important since abnormal retention or DNA contributes pathophysiology sickle disorders. Here we review some key findings so far elucidate importance this various aspects production under homeostasis disease conditions.

Язык: Английский

Процитировано

4

Peroxisome Deficiency in Cochlear Hair Cells Causes Hearing Loss by Deregulating BK Channels DOI Creative Commons
Xiaolong Fu,

Peifeng Wan,

Ling Lü

и другие.

Advanced Science, Год журнала: 2023, Номер 10(20)

Опубликована: Май 12, 2023

Abstract The peroxisome is a ubiquitous organelle in rodent cells and plays important roles variety of cell types tissues. It previously indicated that peroxisomes are associated with auditory function, patients biogenesis disorders (PBDs) found to have hearing dysfunction, but the specific role remains unclear. In this study, two peroxisome‐deficient mouse models ( Atoh1‐Pex5 −/− Pax2‐Pex5 ) established it mainly function hair cochleae. Furthermore, deficiency‐mediated negative effects on do not involve mitochondrial dysfunction oxidative damage. Although mammalian target rapamycin complex 1 (mTORC1) signaling shown through peroxisomes, no changes observed mTORC1 −/‐ mice when compared wild‐type (WT) mice. However, expression large‐conductance, voltage‐, Ca2 + ‐activated K (BK) channels less as WT mice, administration activators BK (NS‐1619 NS‐11021) restores knockout These results suggest play an essential cochlear by regulating channels. Hence, appear probable for treating peroxisome‐related diseases such PBDs.

Язык: Английский

Процитировано

10

Mitochondrial dysfunction in acute kidney injury DOI Creative Commons

Congcong Yao,

Ziwei Li,

Keke Sun

и другие.

Renal Failure, Год журнала: 2024, Номер 46(2)

Опубликована: Авг. 27, 2024

Acute kidney injury (AKI) is a systemic clinical syndrome increasing morbidity and mortality worldwide in recent years. Renal tubular epithelial cells (TECs) death caused by mitochondrial dysfunction one of the pathogeneses. The imbalance quality control main cause dysfunction. Mitochondrial plays crucial role AKI. mechanisms are involved regulating integrity function, including antioxidant defense, control, DNA (mtDNA) repair, dynamics, mitophagy, biogenesis. Currently, many studies have used as targeted therapeutic strategy for Therefore, this review aims to present latest research advancements on AKI, providing valuable reference theoretical foundation prevention treatment condition, ultimately enhancing patient prognosis.

Язык: Английский

Процитировано

4

Mammalian pexophagy at a glance DOI Creative Commons

Justyna Bajdzienko,

Anja Bremm

Journal of Cell Science, Год журнала: 2024, Номер 137(9)

Опубликована: Май 1, 2024

ABSTRACT Peroxisomes are highly plastic organelles that involved in several metabolic processes, including fatty acid oxidation, ether lipid synthesis and redox homeostasis. Their abundance activity dynamically regulated response to nutrient availability cellular stress. Damaged or superfluous peroxisomes removed mainly by pexophagy, the selective autophagy of induced ubiquitylation peroxisomal membrane proteins ubiquitin-independent processes. Dysregulated pexophagy impairs peroxisome homeostasis has been linked development various human diseases. Despite many recent insights into mammalian our understanding this process is still limited compared yeast. In Cell Science at a Glance article accompanying poster, we summarize current knowledge on control highlight which aspects require further attention. We also discuss role describe ubiquitin machinery regulating signals for recruitment phagophores peroxisomes.

Язык: Английский

Процитировано

3