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Mechanical and IL-1β Responsive miR-365 Contributes to Osteoarthritis Development by Targeting Histone Deacetylase 4.
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- المؤلفون: Yang X;Yang X; Guan Y; Guan Y; Tian S; Tian S; Wang Y; Wang Y; Sun K; Sun K; Chen Q; Chen Q
- المصدر:
International journal of molecular sciences [Int J Mol Sci] 2016 Mar 23; Vol. 17 (4), pp. 436. Date of Electronic Publication: 2016 Mar 23.
- نوع النشر :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
- اللغة:
English
- معلومة اضافية
- المصدر:
Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067 (Electronic) Linking ISSN: 14220067 NLM ISO Abbreviation: Int J Mol Sci Subsets: MEDLINE
- بيانات النشر:
Original Publication: Basel, Switzerland : MDPI, [2000-
- الموضوع:
- نبذة مختصرة :
Mechanical stress plays an important role in the initiation and progression of osteoarthritis. Studies show that excessive mechanical stress can directly damage the cartilage extracellular matrix and shift the balance in chondrocytes to favor catabolic activity over anabolism. However, the underlying mechanism remains unknown. MicroRNAs (miRNAs) are emerging as important regulators in osteoarthritis pathogenesis. We have found that mechanical loading up-regulated microRNA miR-365 in growth plate chondrocytes, which promotes chondrocyte differentiation. Here, we explored the role of the mechanical responsive microRNA miR-365 in pathogenesis of osteoarthritis (OA). We found that miR-365 was up-regulated by cyclic loading and IL-1β stimulation in articular chondrocytes through a mechanism that involved the transcription factor NF-κB. miR-365 expressed significant higher level in rat anterior cruciate ligament (ACL) surgery induced OA cartilage as well as human OA cartilage from primary OA patients and traumatic OA Patients. Overexpression of miR-365 in chondrocytes increases gene expression of matrix degrading enzyme matrix metallopeptidase 13 (MMP13) and collagen type X (Col X). The increase in miR-365 expression in OA cartilage and in response to IL-1 may contribute to the abnormal gene expression pattern characteristic of OA. Inhibition of miR-365 down-regulated IL-1β induced MMP13 and Col X gene expression. We further showed histone deacetylase 4 (HDAC4) is a direct target of miR-365, which mediates mechanical stress and inflammation in OA pathogenesis. Thus, miR-365 is a critical regulator of mechanical stress and pro-inflammatory responses, which contributes cartilage catabolism. Manipulation of the expression of miR-365 in articular chondrocytes by miR-365 inhibitor may be a potent therapeutic target for the prevention and treatment of osteoarthritis.
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- Grant Information:
P20 GM104937 United States GM NIGMS NIH HHS
- Contributed Indexing:
Keywords: inflammation; mechanical loading; miR-365; osteoarthritis
- الرقم المعرف:
0 (Interleukin-1beta)
0 (MIRN365 microRNA, human)
0 (MicroRNAs)
0 (NF-kappa B)
0 (Repressor Proteins)
EC 3.4.24.- (Matrix Metalloproteinase 13)
EC 3.5.1.98 (HDAC4 protein, human)
EC 3.5.1.98 (Histone Deacetylases)
- الموضوع:
Date Created: 20160330 Date Completed: 20161220 Latest Revision: 20220330
- الموضوع:
20231215
- الرقم المعرف:
PMC4848892
- الرقم المعرف:
10.3390/ijms17040436
- الرقم المعرف:
27023516
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