TY - JOUR
T1 - Techniques for the Detection of Autophagy in Primary Mammalian Cells
AU - Puleston, Daniel
AU - Phadwal, Kanchan
AU - Watson, Alexander Scarth
AU - Soilleux, Elizabeth J
AU - Chittaranjan, Suganthi
AU - Bortnik, Svetlana
AU - Gorski, Sharon M
AU - Ktistakis, Nicholas
AU - Simon, Anna Katharina
N1 - © 2015 Cold Spring Harbor Laboratory Press.
PY - 2015
Y1 - 2015
N2 - Autophagy is a lysosomal catabolic pathway responsible for the degradation of cytoplasmic constituents. Autophagy is primarily a survival pathway for recycling cellular material in times of nutrient starvation, and in response to hypoxia, endoplasmic reticulum stress, and other stresses, regulated through the mammalian target of rapamycin pathway. The proteasomal pathway is responsible for degradation of proteins, whereas autophagy can degrade cytoplasmic material in bulk, including whole organelles such as mitochondria (mitophagy), bacteria (xenophagy), or lipids (lipophagy). Although signs of autophagy can be present during cell death, it remains controversial whether autophagy can execute cell death in vivo. Here, we will introduce protocols for detecting autophagy in mammalian primary cells by using western blots, immunofluorescence, immunohistochemistry, flow cytometry, and imaging flow cytometry.
AB - Autophagy is a lysosomal catabolic pathway responsible for the degradation of cytoplasmic constituents. Autophagy is primarily a survival pathway for recycling cellular material in times of nutrient starvation, and in response to hypoxia, endoplasmic reticulum stress, and other stresses, regulated through the mammalian target of rapamycin pathway. The proteasomal pathway is responsible for degradation of proteins, whereas autophagy can degrade cytoplasmic material in bulk, including whole organelles such as mitochondria (mitophagy), bacteria (xenophagy), or lipids (lipophagy). Although signs of autophagy can be present during cell death, it remains controversial whether autophagy can execute cell death in vivo. Here, we will introduce protocols for detecting autophagy in mammalian primary cells by using western blots, immunofluorescence, immunohistochemistry, flow cytometry, and imaging flow cytometry.
U2 - 10.1101/pdb.top070391
DO - 10.1101/pdb.top070391
M3 - Article
C2 - 26330629
VL - 2015
SP - pdb.top070391
JO - Cold Spring Harbor protocols
JF - Cold Spring Harbor protocols
SN - 1559-6095
IS - 9
ER -