p62/SQSTM1

Lysosomal Dysfunction is Linked to Exosomal Secretion

Nuclear LC3: Why is it there and what is it doing?

Autophagy inhibition in pediatrics: One physician-scientist’s brave decision

Cleaner gone bad: Autophagy regulates motor neuron loss in spinal muscular atrophy

Cross-talk between proteasome degradation and lysosomal degradation

CaMKII stimulates autophagic degradation of 'ID', a new frontier against cancer

Brain size matters: MTOR regulates autophagy and number of cortical interneurons

Key Targets in Apoptosis, Necroptosis, and Autophagy

Cell death/recycling pathways such as apoptosis, necroptosis, and autophagy are an integral part of the growth, development, homeostasis as well as the pathophysiology in the life of living organisms. These signaling pathways are highly regulated and some of their key regulatory targets are discussed below.

Apoptosis

Apoptosis, programmed cell death, is primarily characterized by the activation of caspases which further regulate the mass cleavage of proteins and DNA. Some of major the proteins responsible for various apoptotic events are:

What are the major differences between Apoptosis, Necroptosis & Autophagy?

Apoptosis is a form of programmed cell death which is mediated by cysteine proteases called caspases. It is an essential phenomenon in the maintenance of homeostasis and growth of tissues, and it also plays a critical role in immune response. The cytomorphological alterations and the key features of apoptosis are listed below:

apoptosis

Required proteins for p62/SQSTM1 regulation and a role for p62/SQSTM1 in neuronal autophagy

Autophagy is a crucial cellular process that clears the cell of protein aggregates, toxins, and damaged cell products. Accumulation of toxins, damaged cell products and unwanted proteins has been proven to play a role in aging and many forms of disease and cancer.

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