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Updated: Feb 8, 2026

Analyzing Starvation-Induced Autophagy in the Drosophila melanogaster Larval Fat Body
Published on: August 4, 2022
Role of the MAPK/cJun NH2-terminal kinase signaling pathway in starvation-induced autophagy
Seda Avcioglu Barutcu1, Nomeda Girnius1, Santiago Vernia1
1a Program in Molecular Medicine , University of Massachusetts Medical School , Worcester , MA , USA.
Abstract:
Autophagy is required for cellular homeostasis and can determine cell viability in response to stress. It is established that MTOR is a master regulator of starvation-induced macroautophagy/autophagy, but recent studies have also implicated an essential role for the MAPK8/cJun NH2-terminal kinase 1 signal transduction pathway. We found that MAPK8/JNK1 and MAPK9/JNK2 were not required for autophagy caused by starvation or MTOR inhibition in murine fibroblasts and epithelial cells. These data demonstrate that MAPK8/9 has no required role in starvation-induced autophagy. We conclude that the role of MAPK8/9 in autophagy may be context-dependent and more complex than previously considered.
Abbreviations:
AKT: thymoma viral proto-oncogene;ALB: albumin; ATG4: autophagy related 4; BCL2: B cell leukemia/lymphoma 2; BECN1: beclin 1, autophagy related; BNIP3: BCL2/adenovirus E1B interacting protein 3; CQ: chloroquine diphosphate; DMEM: Dulbecco's modified Eagle's medium; EDTA: ethylenediaminetetraacetic acid; EBSS: Earle's balanced salt solution; FBS: fetal bovine serum; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; GFP: green fluorescent protein; HRAS: Harvey rat sarcoma virus oncogene; IgG: Immunoglobulin G; MAPK3/ERK1: mitogen-activated protein kinase 3; MAPK8/JNK1: mitogen-activated protein kinase 8; MAPK9/JNK2: mitogen-activated protein kinase 9; MAPK10/JNK3: mitogen-activated protein kinase 10; MAP1LC3B/LC3B: microtubule-associated protein 1 light chain 3 beta; MEFs: mouse embryonic fibroblasts; MTOR: mechanistic target of rapamycin kinase; RPS6KB1/p70: ribosomal protein S6 kinase, polypeptide 1; PPARA: peroxisome proliferator activated receptor alpha; SEM: standard error of the mean; SQSTM1/p62: sequestosome 1; TORC1: target of rapamycin complex 1; TORC2: target of rapamycin complex 2; TRP53: transforming related protein 53; TUBA: tubulin alpha; UV: ultraviolet; WT: wild-type.
Insights
Mitogen-activated protein kinase 8 (MAPK8/JNK1) and MAPK9 are not required for starvation-induced autophagy. These findings suggest the role of MAPK8/9 in autophagy is context-dependent and complex.
Area of Science:
- Cellular Biology
- Molecular Biology
- Biochemistry
Background:
- Autophagy is crucial for cellular homeostasis and survival under stress.
- Mechanistic target of rapamycin (MTOR) is a known regulator of starvation-induced autophagy.
- Recent studies suggested a role for the MAPK8/JNK1 pathway in autophagy.
Purpose of the Study:
- To investigate the role of MAPK8/JNK1 and MAPK9/JNK2 in starvation-induced autophagy.
- To determine if MAPK8/9 signaling is essential for autophagy triggered by MTOR inhibition.
Main Methods:
- Experiments were conducted using murine fibroblasts and epithelial cells.
- Autophagy induction was achieved through starvation and MTOR inhibition.
- The requirement of MAPK8/JNK1 and MAPK9/JNK2 was assessed in these conditions.
Main Results:
- MAPK8/JNK1 and MAPK9/JNK2 were found to be non-essential for autophagy induced by starvation.
- These kinases were also not required for autophagy resulting from MTOR inhibition.
- The data indicate MAPK8/9 does not play a required role in starvation-induced autophagy.
Conclusions:
- MAPK8/JNK1 and MAPK9/JNK2 are not required for starvation-induced autophagy in the studied cell types.
- The previously implicated role of MAPK8/9 in autophagy may be context-specific.
- The precise function of MAPK8/9 in autophagy warrants further investigation due to its complexity.
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