The deficiency of upstream regulators of the mitochondrial death pathway has been recently shown to trigger in vitro a cellular process of self-clearance with features of autophagy. We show here that, when Apaf1 (responsible for apoptosome formation) is downregulated in vivo in cortical precursors, cells express markers of neuronal differentiation, accumulate in ectopic cortical masses and show hallmarks of the beclin-1-dependent pathway of autophagy, probably activated by a depletion in growth factors in the cells' microenvironment. To visualize this process in a cell culture model system, we also used a neural precursor cell line to mimic growth factor starvation in the absence of the apoptosome and tracked autophagolysosome formation. Our findings demonstrate the existence of an interplay between the autophagy and apoptosis pathways in vivo in brain development, and possibly link the absence of apoptosis to the occurrence of pathological conditions associated with peculiar cellular morphotypes.
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http://dx.doi.org/10.1007/s10495-006-9081-4 | DOI Listing |
Cell Death Discov
April 2022
Laboratory of Cell Signaling, Graduate School of Pharmaceutical Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, Japan.
Oxidative stress is a state in which the accumulation of reactive oxygen species exceeds the capacity of cellular antioxidant systems. Both apoptosis and necrosis are observed under oxidative stress, and we have reported that these two forms of cell death are induced in HO-stimulated HeLa cells depending on the concentration of HO. Weak HO stimulation induces apoptosis, while strong HO stimulation induces necrosis.
View Article and Find Full Text PDFEnviron Toxicol Pharmacol
October 2020
Immunobiology Laboratory, Department of Zoology, University of Delhi, Delhi 110007, India; Faculty of Life Sciences & Biotechnology, South Asian University, New Delhi 110 021, India. Electronic address:
Multidrug-resistance protein-1 facilitates the efflux of arsenic conjugated with reduced glutathione nonetheless; the relation between Mrp-1 ATPase activity and cellular GSH levels is contentious. To study this, Mrp-1-ATPase activity was measured in 5 μM arsenic trioxide exposed zebrafish hepatocytes (ZFH) and correlated with intracellular GSH levels. Alongside, mrp-1 gene expression as well as Mrp-1 protein level was also monitored.
View Article and Find Full Text PDFPLoS One
February 2020
Department of Neurobiology, Gifu University Graduate School of Medicine, Yanagido, Gifu, Japan.
Biosci Rep
May 2019
Department of Pathology and Pathophysiology, Key Laboratory of Disease Proteomics of Zhejiang Province, School of medicine, Zhejiang University, Hangzhou, Zhejiang Province, China
Human breast cancer is a malignant form of tumor with a relatively high mortality rate. Although esophageal cancer-related gene 4 (ECRG4) is thought to be a possible potent tumor suppressor gene that acts to suppress breast cancer, its precise role in this disease is not understood. Herein, we assess the correlation between ECRG4 expression and DNA methylation, probing the potential epigenetic regulation of ECRG4 in breast cancer.
View Article and Find Full Text PDFGene
December 2018
Department of Genetics, Osmania University, Hyderabad, Telangana, India. Electronic address:
Introduction: Chronic Myeloid Leukemia (CML) is a myeloproliferative disorder, characterized by the overproduction of myeloid cells in all stages of maturation. It is usually defined by three sequential stages (Chronic, Accelerated and Blast-crisis) where the transition from chronic to accelerated to blast phases is presumed to occur due to secondary genetic changes, viz. accumulation of mutations, activation of downstream pathways and failure of apoptosis.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!