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1.
Molecules ; 28(12)2023 Jun 09.
Article in English | MEDLINE | ID: mdl-37375217

ABSTRACT

Chondrocytes are surrounded by a lower oxygen environment than other well-vascularized tissues with higher oxygenation levels. Prolyl-hydroxyproline (Pro-Hyp), one of the final collagen-derived peptides, has been previously reported to be involved in the early stages of chondrocyte differentiation. However, whether Pro-Hyp can alter chondrocyte differentiation under physiological hypoxic conditions is still unclear. This study aimed to investigate whether Pro-Hyp affects the differentiation of ATDC5 chondrogenic cells under hypoxic conditions. The addition of Pro-Hyp resulted in an approximately 18-fold increase in the glycosaminoglycan staining area compared to the control group under hypoxic conditions. Moreover, Pro-Hyp treatment significantly upregulated the expression of SOX9, Col2a1, Aggrecan, and MMP13 in chondrocytes cultured under hypoxic conditions. These results demonstrate that Pro-Hyp strongly promotes the early differentiation of chondrocytes under physiological hypoxic conditions. Therefore, Pro-Hyp, a bioactive peptide produced during collagen metabolism, may function as a remodeling factor or extracellular matrix remodeling signal that regulates chondrocyte differentiation in hypoxic cartilage.


Subject(s)
Chondrocytes , Collagen , Chondrocytes/metabolism , Collagen/metabolism , Dipeptides/pharmacology , Dipeptides/metabolism , Cell Differentiation/physiology , Peptides/pharmacology , Peptides/metabolism , Cells, Cultured
2.
Biosci Biotechnol Biochem ; 87(2): 148-157, 2023 Jan 24.
Article in English | MEDLINE | ID: mdl-36441013

ABSTRACT

Lukianol A (1a) and its six derivatives 1b-1g, in which each hydroxyl groups of 1a was individually modified, were synthesized via the common intermediate 7a, which was obtained by condensation of the styryl carbazate 10 with p-hydroxyphenylpyruvic acid and subsequent [3,3]-sigmatropic rearrangement. The synthesized lukianol derivatives were evaluated for their ability to inhibit human aldose reductase. 4'-O-methyl (1b) and 4'-dehydroxy (1g) derivatives showed the same level of inhibitory activity as 1a (IC50 2.2 µm), indicating that the 4'-OH is irrelevant for the activity. In contrast, methylation of the hydroxyl group at the 4″'-position (1d) resulted in the loss of activity at a concentration of 10 µm, and masking the hydroxyl group at the 4″-position (1e) caused a 9-fold decrease in activity compared with that of 1b, suggesting that the 4″-OH is an essential group, and the 4″'-OH is required for higher activity.


Subject(s)
Alkaloids , Antineoplastic Agents , Humans , Aldehyde Reductase/metabolism , Enzyme Inhibitors/pharmacology , Structure-Activity Relationship , Antineoplastic Agents/pharmacology
3.
Electrophoresis ; 41(15): 1316-1325, 2020 08.
Article in English | MEDLINE | ID: mdl-32386342

ABSTRACT

Acid dissociation constants (pKa ) of nine kinds of flavin analogues as molecular catalyst candidates were determined by CZE. Although some of the analogues are instable and degradable under the light exposure or in alkaline aqueous solutions, the effective electrophoretic mobility of the flavin analogue of interest has been measured with the residual substance. The pKa values of the flavin analogues were analyzed through the changes in the effective electrophoretic mobility with varying pH of the separation buffer. One or two steps pKa values were determined by the analysis. One of the degraded species from the flavin analogues, lumichrome, was also detected in the CZE analysis, and its pKa values were also determined. While coexisting impurities generated over the storage conditions were found in some analogues, the pKa values of the target analogues were successfully determined with the help of the CZE separations. A pressure-assisted CZE was utilized for the determination or the estimation of the pKa values of such analogues as possessing carboxylic acid moiety.


Subject(s)
Acids/chemistry , Electrophoresis, Capillary/methods , Flavins , Chemical Phenomena , Flavins/analysis , Flavins/chemistry , Flavins/isolation & purification , Hydrogen-Ion Concentration
4.
Vet Dermatol ; 27(3): 184-e46, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27018172

ABSTRACT

BACKGROUND: Colonization, overgrowth and subsequent infection by Staphylococcus spp. is frequently observed in canine atopic dermatitis (CAD), where it contributes to the intensity of cutaneous inflammation. The mechanisms by which staphylococci contribute to the pathogenesis of CAD are unclear. Studies suggest that thymic stromal lymphopoietin (TSLP), a cytokine induced by a cell wall component of Staphylococcus spp., may play a critical role in Th2 responses including the pathogenesis of CAD. HYPOTHESIS/OBJECTIVE: To determine if synthetic triacylated lipopeptide (TLR1/2 ligand), a cell wall component of Staphylococcus spp., induces the transcription of TSLP via TLR2 in canine keratinocytes. METHODS: Transcription of TSLP was quantified in a canine keratinocyte cell line after stimulation with synthetic triacylated lipopeptide, and again after inhibition of TLR2 by a targeted small interfering RNA. RESULTS: The transcription of TSLP was enhanced 6 h after stimulation with the synthetic triacylated lipopeptide; it was completely suppressed by knockdown of TLR2. CONCLUSIONS AND CLINICAL IMPORTANCE: The results demonstrated that a synthetic cell wall component of Staphylococcus spp. induced transcription of TSLP via TLR2 in canine keratinocytes. Additional studies will be required to investigate whether Staphylococcus spp. contributes to Th2 responses in CAD through TLR2-mediated TSLP production.


Subject(s)
Cytokines/metabolism , Dermatitis, Atopic/veterinary , Dog Diseases/metabolism , Keratinocytes/metabolism , Staphylococcus , Toll-Like Receptor 2/metabolism , Animals , Cytokines/genetics , Dermatitis, Atopic/complications , Dermatitis, Atopic/metabolism , Dog Diseases/etiology , Dog Diseases/pathology , Dogs , Gene Expression Regulation/immunology , Hypersensitivity/veterinary , Inflammation/metabolism , Inflammation/veterinary , Staphylococcal Skin Infections/complications , Staphylococcal Skin Infections/metabolism , Staphylococcal Skin Infections/veterinary , Toll-Like Receptor 2/genetics , Thymic Stromal Lymphopoietin
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