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A potent endocytosis inhibitor Ikarugamycin up-regulates TNF production
- Source :
- Biochemistry and Biophysics Reports, Vol 27, Iss, Pp 101065-(2021), Biochemistry and Biophysics Reports
- Publication Year :
- 2021
- Publisher :
- Elsevier BV, 2021.
-
Abstract
- Ikarugamycin (IK) is an antibiotic which has been reported to have a variety of functions, such as inhibition of clathrin-mediated endocytosis (CME), anti-tumor effects and regulation of the immune system. Whether IK influences cytokine production is poorly understood. We have investigated the relationship between IK and production of tumor necrosis factor-α (TNF). TNF plays a pivotal role in pathogenesis of many diseases. Although the dynamics of soluble TNF (sTNF) has been widely explored so far, the functions of the membrane form of TNF (mTNF) have not been fully elucidated. We demonstrated that IK increases the amount of mTNF and prolongs the duration of TNF expression. This effect is unrelated to the shedding activity of disintegrin and metalloproteinase domain-containing protein 17 (ADAM 17). Our results revealed that there is a mechanism to terminate inflammation at the cellular level which IK dysregulates. Furthermore, IK can be a tool to study TNF signaling due to its effect of increasing mTNF expression.
- Subjects :
- Ikarugamycin
QH301-705.5
Short Communication
medicine.medical_treatment
mTNF, membrane form of TNF
TNF
Biophysics
Inflammation
QD415-436
CME, clathrin-mediated endocytosis
TNF, tumor necrosis factor-α
Endocytosis
Biochemistry
Pathogenesis
Immune system
medicine
Disintegrin
Biology (General)
IK, ikarugamycin
Metalloproteinase
biology
Chemistry
Cell biology
sTNF, soluble TNF
TAPI-1, TNF alpha processing inhibitor-1
Cytokine
ADAM 17, disintegrin and metalloproteinase domain-containing protein 17
biology.protein
LPS, lipopolysaccharide
Tumor necrosis factor alpha
medicine.symptom
TNFR, TNF receptor
Subjects
Details
- ISSN :
- 24055808
- Volume :
- 27
- Database :
- OpenAIRE
- Journal :
- Biochemistry and Biophysics Reports
- Accession number :
- edsair.doi.dedup.....f482f004afe8c745a364c5d5502fc1f4