Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
1.
Cell Mol Life Sci ; 81(1): 154, 2024 Mar 28.
Article in English | MEDLINE | ID: mdl-38538857

ABSTRACT

Approximately 60% of septic patients developed acute kidney injury (AKI). The mortality rate of septic AKI (SA-AKI) is two to three times higher than that of septic without AKI (SA-non-AKI). The actual functions and mechanisms of CircRNAs in the pathophysiology of SA-AKI remain incompletely understood. Herein, we observed that the mmu_Circ_26986 could be induced by lipopolysaccharide (LPS) and cecum ligation and puncture (CLP) in BUMPT cell line and C57BL/6 mouse kidney, respectively. Functionally, mmu_Circ_26986 suppressed BUMPT cell apoptosis induced by LPS. Mechanistically, mmu_Circ_26986 sponged miRNA-29b-1-5p to upregulate the expression of PAK7. Overexpression of mmu_Circ_26986 ameliorated the progression of CLP-stimulated AKI through miRNA-29b-1-5p/PAK7 axis. In addition, we found that hsa_Circ_0072463, homologous to mmu_Circ_26986, suppressed LPS-induced HK-2 cells apoptosis via regulation of miRNA-29b-1-5p/PAK7 axis. Furthermore, sepsis patients with AKI had a higher level of hsa_Circ_0072463 compared to those without AKI. The sensitivity, specificity and AUC of hsa_Circ_0072463 were 78.8%, 87.9% and 0.866, respectively. Spearman's test indicated a noticeable positive correlation between plasma hsa_Circ_0072463 and serum creatinine in sepsis patients (r = 0.725). In summary, this study reveals that the mmu_Circ_26986/hsa_Circ_0072463 miRNA-29b-1-5p/PAK7 axis mediates septic AKI, and hsa_Circ_0072463 is a potential diagnostic marker for septic AKI.


Subject(s)
Acute Kidney Injury , MicroRNAs , Sepsis , Mice , Animals , Humans , Mice, Inbred C57BL , Lipopolysaccharides/pharmacology , Acute Kidney Injury/genetics , MicroRNAs/genetics , Sepsis/complications , Sepsis/genetics , Apoptosis/genetics , Biomarkers
2.
Mol Med ; 29(1): 9, 2023 01 18.
Article in English | MEDLINE | ID: mdl-36653745

ABSTRACT

BACKGROUND: Retinal ganglion cells (RGCs) apoptosis is a vital manifestation of retinal ischemia/reperfusion (I/R) injury, yet the underlying mechanisms are not well understood. The contribution of long noncoding RNAs (lncRNAs) to this cellular process is currently being explored. Based on a lncRNA chip assay, we aimed to investigate the role of lncRNA uc007nnj.1 in the pathological process of ischemia-induced RGCs apoptosis. METHODS: Hank's balanced salt solution containing 10 µM antimycin A and 2 µM calcium ionophore for 2 h to construct an ischemic model in RGCs, and elevation of intraocular pressure to 120 mm Hg for 1 h was used to construct a mouse model of retinal I/R injury. RESULTS: In this study, lncRNA uc007nnj.1 was highly upregulated in response to I/R injury in RGCs and mouse retinas. In addition, lncRNA uc007nnj.1 knockdown reduced retinal neuronal cell apoptosis in vitro and in vivo and significantly improved retinal function. DISCUSSION: Mechanistically, the results demonstrated that lncRNA uc007nnj.1 acts as ceRNA competitively binding miR-155-5p, thereby enhancing the expression levels of Tle4, thus aggravating ischemia-related apoptosis in RGCs. CONCLUSIONS: Finally, our study identifies the lncRNA uc007nnj.1/miR-155-5p/Tle4 axis as a potential target for the prevention of I/R-induced retinal neuronal death.


Subject(s)
MicroRNAs , RNA, Long Noncoding , Reperfusion Injury , Mice , Animals , RNA, Long Noncoding/genetics , RNA, Long Noncoding/metabolism , MicroRNAs/genetics , MicroRNAs/metabolism , Reperfusion , Reperfusion Injury/metabolism , Apoptosis/genetics , Ischemia , Repressor Proteins
3.
IEEE Trans Neural Netw Learn Syst ; 23(6): 876-88, 2012 Jun.
Article in English | MEDLINE | ID: mdl-24806760

ABSTRACT

As one of the fundamental features, color provides useful information and plays an important role for face recognition. Generally, the choice of a color space is different for different visual tasks. How can a color space be sought for the specific face recognition problem? To address this problem, we propose a sparse tensor discriminant color space (STDCS) model that represents a color image as a third-order tensor in this paper. The model cannot only keep the underlying spatial structure of color images but also enhance robustness and give intuitionistic or semantic interpretation. STDCS transforms the eigenvalue problem to a series of regression problems. Then one spare color space transformation matrix and two sparse discriminant projection matrices are obtained by applying lasso or elastic net on the regression problems. The experiments on three color face databases, AR, Georgia Tech, and Labeled Faces in the Wild face databases, show that both the performance and the robustness of the proposed method outperform those of the state-of-the-art TDCS model.


Subject(s)
Biometry/methods , Colorimetry/methods , Face/anatomy & histology , Image Interpretation, Computer-Assisted/methods , Pattern Recognition, Automated/methods , Artificial Intelligence , Color , Humans , Reproducibility of Results , Sensitivity and Specificity
SELECTION OF CITATIONS
SEARCH DETAIL
...