TY - JOUR
T1 - Activation of IRE1, PERK and salt-inducible kinases leads to Sec body formation in Drosophila S2 cells
AU - Zhang, Chujun
AU - van Leeuwen, Wessel
AU - Blotenburg, Marloes
AU - Aguilera-Gomez, Angelica
AU - Brussee, Sem
AU - Grond, Rianne
AU - Kampinga, Harm H.
AU - Rabouille, Catherine
N1 - Funding Information:
We thank our colleagues in the field for critics and comments. We thank Apfrida Kendek (UMCU) for Fig. S2C. We acknowledge Genentech for providing us with the AMG18 and the anti IRE1-p monoclonal antibody. C.Z. is supported by a scholarship of the China Scholarship Council (201706670014). Deposited in PMC for immediate release.
Funding Information:
C.Z. is supported by a scholarship of the China Scholarship Council (201706670014). Deposited in PMC for immediate release.
Publisher Copyright:
© 2021. Published by The Company of Biologists Ltd.
PY - 2021/9/1
Y1 - 2021/9/1
N2 - The phase separation of the non-membrane bound Sec bodies occurs in Drosophila S2 cells by coalescence of components of the endoplasmic reticulum (ER) exit sites under the stress of amino acid starvation. Here, we address which signaling pathways cause Sec body formation and find that two pathways are critical. The first is the activation of the salt-inducible kinases (SIKs; SIK2 and SIK3) by Na
+ stress, which, when it is strong, is sufficient. The second is activation of IRE1 and PERK (also known as PEK in flies) downstream of ER stress induced by the absence of amino acids, which needs to be combined with moderate salt stress to induce Sec body formation. SIK, and IRE1 and PERK activation appear to potentiate each other through the stimulation of the unfolded protein response, a key parameter in Sec body formation. This work shows the role of SIKs in phase transition and re-enforces the role of IRE1 and PERK as a metabolic sensor for the level of circulating amino acids and salt.
AB - The phase separation of the non-membrane bound Sec bodies occurs in Drosophila S2 cells by coalescence of components of the endoplasmic reticulum (ER) exit sites under the stress of amino acid starvation. Here, we address which signaling pathways cause Sec body formation and find that two pathways are critical. The first is the activation of the salt-inducible kinases (SIKs; SIK2 and SIK3) by Na
+ stress, which, when it is strong, is sufficient. The second is activation of IRE1 and PERK (also known as PEK in flies) downstream of ER stress induced by the absence of amino acids, which needs to be combined with moderate salt stress to induce Sec body formation. SIK, and IRE1 and PERK activation appear to potentiate each other through the stimulation of the unfolded protein response, a key parameter in Sec body formation. This work shows the role of SIKs in phase transition and re-enforces the role of IRE1 and PERK as a metabolic sensor for the level of circulating amino acids and salt.
KW - Drosophila S2 cells
KW - Amino acid starvation
KW - Phase separation
KW - Salt stress
KW - Sec body
KW - Unfolded protein response
KW - eIF-2 Kinase/genetics
KW - Humans
KW - Unfolded Protein Response
KW - Animals
KW - Endoplasmic Reticulum Stress
KW - Drosophila/metabolism
KW - Protein Serine-Threonine Kinases/genetics
UR - http://www.scopus.com/inward/record.url?scp=85115896833&partnerID=8YFLogxK
U2 - 10.1242/jcs.258685
DO - 10.1242/jcs.258685
M3 - Article
C2 - 34350957
AN - SCOPUS:85115896833
SN - 1477-9137
VL - 134
JO - Journal of cell science
JF - Journal of cell science
IS - 17
M1 - jcs258685
ER -