[HTML][HTML] Peroxisomes: a nexus for lipid metabolism and cellular signaling

IJ Lodhi, CF Semenkovich - Cell metabolism, 2014 - cell.com
Peroxisomes are often dismissed as the cellular hoi polloi, relegated to cleaning up reactive
oxygen chemical debris discarded by other organelles. However, their functions extend far …

[HTML][HTML] Peroxisome quality control and dysregulated lipid metabolism in neurodegenerative diseases

DS Jo, NY Park, DH Cho - Experimental & molecular medicine, 2020 - nature.com
In recent decades, the role of the peroxisome in physiology and disease conditions has
become increasingly important. Together with the mitochondria and other cellular …

[HTML][HTML] Genetics and molecular basis of human peroxisome biogenesis disorders

HR Waterham, MS Ebberink - … et Biophysica Acta (BBA)-Molecular Basis of …, 2012 - Elsevier
Human peroxisome biogenesis disorders (PBDs) are a heterogeneous group of autosomal
recessive disorders comprised of two clinically distinct subtypes: the Zellweger syndrome …

β-Oxidation of fatty acids in mitochondria, peroxisomes, and bacteria: a century of continued progress

WH Kunau, V Dommes, H Schulz - Progress in lipid research, 1995 - Elsevier
Almost a century has passed since Knoop performed his classical feeding experiments that
led him to propose the principle of fl-oxidation for the degradation of fatty acids. After …

[HTML][HTML] Peroxisome-derived lipids regulate adipose thermogenesis by mediating cold-induced mitochondrial fission

H Park, A He, M Tan, JM Johnson… - The Journal of …, 2019 - Am Soc Clin Investig
Peroxisomes perform essential functions in lipid metabolism, including fatty acid oxidation
and plasmalogen synthesis. Here, we describe a role for peroxisomal lipid metabolism in …

Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata

N Braverman, G Steel, C Obie, A Moser, H Moser… - Nature …, 1997 - nature.com
Rhizomelic chondrodysplasia punctata (RCDP) is a rare autosomal recessive phenotype
that comprises complementation group 11 of the peroxisome biogenesis disorders (PBD) …

[HTML][HTML] Peroxisome-mediated metabolism is required for immune response to microbial infection

F Di Cara, A Sheshachalam, NE Braverman… - Immunity, 2017 - cell.com
The innate immune response is critical for animal homeostasis and is conserved from
invertebrates to vertebrates. This response depends on specialized cells that recognize …

[HTML][HTML] Pexophagy: a model for selective autophagy

K Germain, PK Kim - International journal of molecular sciences, 2020 - mdpi.com
The removal of damaged or superfluous organelles from the cytosol by selective autophagy
is required to maintain organelle function, quality control and overall cellular homeostasis …

An oligomeric protein is imported into peroxisomes in vivo.

JA McNew, JM Goodman - The Journal of cell biology, 1994 - rupress.org
The mechanism of translocation of peroxisomal proteins from the cytoplasm into the matrix is
largely unknown. We have been studying this problem in yeast. We show that the …

PEX3 functions as a PEX19 docking factor in the import of class I peroxisomal membrane proteins

Y Fang, JC Morrell, JM Jones, SJ Gould - The Journal of cell biology, 2004 - rupress.org
PEX19 is a chaperone and import receptor for newly synthesized, class I peroxisomal
membrane proteins (PMPs). PEX19 binds these PMPs in the cytoplasm and delivers them to …