scholarly journals Nicotinamide (aka Niacinamide) Mitigates SASP-Related Inflammation Induced by Environmental Stressors in Human Epidermal Keratinocytes

2020 ◽  
Author(s):  
John C. Bierman ◽  
Timothy Laughlin ◽  
Makio Tamura ◽  
Ben C. Hulette ◽  
Catherine E. Mack ◽  
...  
Keyword(s):  
Inflammatory Response ◽  
Morphological Changes ◽  
Cell Cycle Control ◽  
Expression Patterns ◽  
Skin Surface ◽  
Environmental Stressors ◽  
Premature Aging ◽  
Cellular Damage ◽  
Epidermal Keratinocytes ◽  
Human Epidermal Keratinocytes

Daily exposure of skin to environmental stressors leads to molecular and morphological changes ascribed as premature aging. These stressors include solar radiation, industrial pollution, fossil fuel and carbon emissions, which cause cellular damage that induces an inflammatory response in skin. Several inflammatory components are known to be involved in triggering the senescence-associated secretory phenotype (SASP) which is known to accelerate aging. It is hypothesized that preventing induction of inflammation by environmental stressors can prevent premature aging. Since it is known that nicotinamide (Nam) has anti-inflammatory properties, we tested whether Nam can inhibit environmental stressor-induced inflammation. Exposure of keratinocytes to UVB, urban dust, diesel exhaust, and cigarette smoke extract stimulated production of the inflammatory mediators PGE2, IL-6, and IL-8 and induced gene expression patterns associated with apoptosis, DNA repair, and cell cycle control. In all cases, Nam treatment significantly inhibited these stress-induced responses. Nam also reduced IL-8 levels stimulated by the combination of topically applied particulate matter (PM2.5) and UV exposure in 3D skin equivalents. Under 5% 02 conditions that more closely mimic physiological 02 levels, Nam had a heightened inhibitory effect on UVB-induced PGE2 levels in keratinocytes. In a UV-challenge study, treatment with Nam reduced skin surface IL-1RA/IL-1 inflammatory biomarkers and erythema that were induced by solar simulated radiation. These findings provide a body of evidence that Nam can mitigate in part the skin’s inflammatory response elicited by exposure to environmental stressors. This supports the potential that Nam can inhibit premature aging and help maintain skin’s functionality and appearance.

scholarly journals Differential and Overlapping Effects of 20,23(OH)2D3 and 1,25(OH)2D3 on Gene Expression in Human Epidermal Keratinocytes: Identification of AhR as an Alternative Receptor for 20,23(OH)2D3

2018 ◽  
Vol 19 (10) ◽  
pp. 3072 ◽  
Author(s):  
Andrzej Slominski ◽  
Tae-Kang Kim ◽  
Zorica Janjetovic ◽  
Anna Brożyna ◽  
Michal Żmijewski ◽  
...  
Keyword(s):  
Gene Expression ◽  
Molecular Modeling ◽  
Vitamin D3 ◽  
Expression Profiles ◽  
Expression Patterns ◽  
Canonical Pathway ◽  
Epidermal Keratinocytes ◽  
Hydroxyl Groups ◽  
Dependent Manner ◽  
Human Epidermal Keratinocytes

A novel pathway of vitamin D activation by CYP11A has previously been elucidated. To define the mechanism of action of its major dihydroxy-products, we tested the divergence and overlap between the gene expression profiles of human epidermal keratinocytes treated with either CYP11A1-derived 20,23(OH)2D3 or classical 1,25(OH)2D3. Both secosteroids have significant chemical similarity with the only differences being the positions of the hydroxyl groups. mRNA was isolated and examined by microarray analysis using Illumina’s HumanWG-6 chip/arrays and subsequent bioinformatics analyses. Marked differences in the up- and downregulated genes were observed between 1,25(OH)2D3- and 20,23(OH)2D3-treated cells. Hierarchical clustering identified both distinct, opposite and common (overlapping) gene expression patterns. CYP24A1 was a common gene strongly activated by both compounds, a finding confirmed by qPCR. Ingenuity pathway analysis identified VDR/RXR signaling as the top canonical pathway induced by 1,25(OH)2D3. In contrast, the top canonical pathway induced by 20,23(OH)2D3 was AhR, with VDR/RXR being the second nuclear receptor signaling pathway identified. QPCR analyses validated the former finding by revealing that 20,23(OH)2D3 stimulated CYP1A1 and CYP1B1 gene expression, effects located downstream of AhR. Similar stimulation was observed with 20(OH)D3, the precursor to 20,23(OH)2D3, as well as with its downstream metabolite, 17,20,23(OH)3D3. Using a Human AhR Reporter Assay System we showed marked activation of AhR activity by 20,23(OH)2D3, with weaker stimulation by 20(OH)D3. Finally, molecular modeling using an AhR LBD model predicted vitamin D3 hydroxyderivatives to be good ligands for this receptor. Thus, our microarray, qPCR, functional studies and molecular modeling indicate that AhR is the major receptor target for 20,23(OH)2D3, opening an exciting area of investigation on the interaction of different vitamin D3-hydroxyderivatives with AhR and the subsequent downstream activation of signal transduction pathways in a cell-type-dependent manner.

Niacinamide mitigates SASP‐related inflammation induced by environmental stressors in human epidermal keratinocytes and skin

2020 ◽  
Vol 42 (5) ◽  
pp. 501-511 ◽  
Author(s):  
John C. Bierman ◽  
Timothy Laughlin ◽  
Makio Tamura ◽  
Ben C. Hulette ◽  
Catherine E. Mack ◽  
...  
Keyword(s):  
Environmental Stressors ◽  
Epidermal Keratinocytes ◽  
Human Epidermal Keratinocytes

Amygdalin Analogues Inhibit IFN-γ Signalling and Reduce the Inflammatory Response in Human Epidermal Keratinocytes

Inflammation ◽  
2013 ◽  
Vol 36 (6) ◽  
pp. 1316-1326 ◽  
Author(s):  
Iole Paoletti ◽  
Vincenza De Gregorio ◽  
Adone Baroni ◽  
Maria Antonietta Tufano ◽  
Giovanna Donnarumma ◽  
...  
Keyword(s):  
Inflammatory Response ◽  
Epidermal Keratinocytes ◽  
Human Epidermal Keratinocytes ◽  
Ifn Γ

scholarly journals Differential Marker Expression between Keratinocyte Stem Cells and Their Progeny Generated from a Single Colony

2021 ◽  
Vol 22 (19) ◽  
pp. 10810
Author(s):  
Dema Ali ◽  
Dana Alhattab ◽  
Hanan Jafar ◽  
Malak Alzubide ◽  
Nour Sharar ◽  
...  
Keyword(s):  
Stem Cells ◽  
Wound Repair ◽  
Expression Patterns ◽  
Epidermal Keratinocytes ◽  
Stem Cell Markers ◽  
Potential Candidate ◽  
Human Epidermal Keratinocytes ◽  
Differentiated Cells ◽  
Clonogenic Potential ◽  
Keratinocyte Stem Cells

The stemness in keratinocyte stem cells (KSCs) is determined by their gene expression patterns. KSCs are crucial in maintaining epidermal homeostasis and wound repair and are widely used candidates for therapeutic applications. Although several studies have reported their positive identifiers, unique biomarkers for KSCs remain elusive. Here, we aim to identify potential candidate stem cell markers. Human epidermal keratinocytes (HEKs) from neonatal foreskin tissues were isolated and cultured. Single-cell clonal analysis identified and characterized three types of cells: KSCs (holoclones), transient amplifying cells (TACs; meroclones), and differentiated cells (DSCs; paraclones). The clonogenic potential of KSCs demonstrated the highest proliferation potential of KSCs, followed by TACs and DSCs, respectively. Whole-transcriptome analysis using microarray technology unraveled the molecular signatures of these cells. These results were validated by quantitative real-time polymerase chain reaction and flow cytometry analysis. A total of 301 signature upregulated and 149 downregulated differentially expressed genes (DEGs) were identified in the KSCs, compared to TACs and DSCs. Furthermore, DEG analyses revealed new sets of genes related to cell proliferation, cell adhesion, surface makers, and regulatory factors. In conclusion, this study provides a useful source of information for the identification of potential SC-specific candidate markers.

Leptin regulates the pro-inflammatory response in human epidermal keratinocytes

2018 ◽  
Vol 310 (4) ◽  
pp. 351-362 ◽  
Author(s):  
Moonyoung Lee ◽  
Eunyoung Lee ◽  
Sun Hee Jin ◽  
Sungjin Ahn ◽  
Sae On Kim ◽  
...  
Keyword(s):  
Inflammatory Response ◽  
Epidermal Keratinocytes ◽  
Human Epidermal Keratinocytes

Alterations of ultrastructure and elemental composition in cultured human epidermal keratinocytes after treatment with nitrofurazone and silver sulfadiazine

1987 ◽  
Vol 45 ◽  
pp. 676-677
Author(s):  
A. R. Crooker ◽  
M. C. Myers ◽  
T. L. Beard ◽  
E. S. Graham
Keyword(s):  
Electron Microscopy ◽  
Elemental Composition ◽  
Pyrolytic Carbon ◽  
Human Keratinocytes ◽  
Silver Sulfadiazine ◽  
Epidermal Keratinocytes ◽  
Human Epidermal Keratinocytes ◽  
Culture Systems ◽  
Cytotoxicity Endpoints

Cell culture systems have become increasingly popular as a means of screening toxic agents and studying toxic mechanisms of drugs and other chemicals at the cellular and subcellular levels. These in vitro tests can be conducted rapidly in a broad range of relevant mammalian culture systems; a variety of biological and biochemical cytotoxicity endpoints can be examined. The following study utilized human keratinocytes to evaluate the relative cytotoxicities of nitrofurazone (NF) and silver sulfadiazine (SS), the active ingredients of FURACIN(R) Topical Cream and SILVADENE(R) Cream, respectively. These compounds are anti-infectives used in the treatment of burn patients. Cell ultrastructure and elemental composition were utilized as cytotoxicity endpoints.Normal Human Epidermal Keratinocytes (HK) were prepared from the EpiPackTM culture system (Clonetics Corporation, Boulder, CO). For scanning electron microscopy (SEM) and transmission electron microscopy (TEM), cells were seeded on sterile 35 mm Falcon plastic dishes; for elemental microanalysis, cells were plated on polished pyrolytic carbon discs (E. Fullam, Latham, NY) placed in the culture dishes.

scholarly journals Inactivation of Bacteria Using Bioactive Nanoparticles and Alternating Magnetic Fields

Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 342
Author(s):  
Vitalij Novickij ◽  
Ramunė Stanevičienė ◽  
Rūta Gruškienė ◽  
Kazimieras Badokas ◽  
Juliana Lukša ◽  
...  
Keyword(s):  
Magnetic Fields ◽  
Foodborne Pathogens ◽  
Morphological Changes ◽  
Foodborne Pathogen ◽  
Cellular Damage ◽  
Suitable Model ◽  
Log Reduction ◽  
Invasive Infections ◽  
Alternating Magnetic Fields ◽  
Inactivation Of Bacteria

Foodborne pathogens are frequently associated with risks and outbreaks of many diseases; therefore, food safety and processing remain a priority to control and minimize these risks. In this work, nisin-loaded magnetic nanoparticles were used and activated by alternating 10 and 125 mT (peak to peak) magnetic fields (AMFs) for biocontrol of bacteria Listeria innocua, a suitable model to study the inactivation of common foodborne pathogen L. monocytogenes. It was shown that L. innocua features high resistance to nisin-based bioactive nanoparticles, however, application of AMFs (15 and 30 min exposure) significantly potentiates the treatment resulting in considerable log reduction of viable cells. The morphological changes and the resulting cellular damage, which was induced by the synergistic treatment, was confirmed using scanning electron microscopy. The thermal effects were also estimated in the study. The results are useful for the development of new methods for treatment of the drug-resistant foodborne pathogens to minimize the risks of invasive infections. The proposed methodology is a contactless alternative to the currently established pulsed-electric field-based treatment in food processing.

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