• 대한화장품학회지
• /
• 제39권1호
• /
• pp.9-17
• /
• 2013

본 논문에서는 세리신잠 실샘 가수분해물(Sericinjam Gland Hydrolysate: SJGH)을 이용하여 진피 섬유아세포에서 항산화 및 항노화 연구를 진행하였다. SJGH는 사람 섬유아세포에서 고농도의 과산화수소에 의한 세포사멸과 세포 내 산화 증가를 효과적으로 방어하였다. 또한 SJGH는 저농도의 과산화수소에 의한 섬유아세포의 SA-${\beta}$-Gal 발현과 MMP-1의 발현 증가를 억제하였고, 반대로 프로콜라겐 I의 생합성은 증가시켰다. 이러한 결과를 통해 SJGH의 항산화 및 항노화 효과가 우수함을 확인하였으며, SJGH가 항노화 화장품의 우수한 소재가 될 수 있음을 보여준다.

• 한국자원식물학회지
• /
• 제27권3호
• /
• pp.215-222
• /
• 2014

This study was conducted to isolate a compound with anticancer properties from the roots of Peucedanum japonicum Thunb. (Umbelliferae), and to evaluate the efficacy of that compound's anticancer activity. The $CHCl_3$ layer was purified via repeated column chromatography and recrystallization. The two compounds isolated from $CHCl_3$ layer were identified via NMR spectroscopic analysis as (10E) 1,10-heptadecadiene-4,6-diyne-3,8,9-triol (Comp. I) and anomalin (Comp. II). (10E) 1,10-heptadecadiene-4,6-diyne-3,8,9-triol was the first report from the roots of P. japonicum. MTT assays were conducted to evaluate the in vitro cytotoxic activities of Compounds I and II against the following human cancer cell lines: HeLa, HepG2, SNU-16, and AGS. Comp. I evidenced the most profound cytotoxic activity against HepG2 cells ($IC_{50}=6.04{\mu}g/mL$), and Comp. II exhibited the most profound cytotoxic activity against SNU-16 cells ($IC_{50}=18.24{\mu}g/mL$) among the human cancer cell lines tested in this study. However, no significant cell death was observed in the CCD-25Lu human normal lung fibroblast cells. Quantitative analysis using UPLC (Ultra Performance Liquid Chromatography) showed that the roots of P. japonicum contained 0.015 (Comp. I) and 1.69 mg/g (Comp. II) of these compounds.

• Molecules and Cells
• /
• 제41권5호
• /
• pp.436-443
• /
• 2018

The actin cytoskeleton plays a key role in the entry of mitosis as well as in cytokinesis. In a previous study, we showed that actin disruption delays mitotic entry at G2/M by sustained activation of extracellular signal-related kinase 1/2 (ERK1/2) in primary cells but not in transformed cancer cell lines. Here, we examined the mechanism of cell cycle delay at G2/M by actin dysfunction in IMR-90 normal human fibroblasts. We observed that de-polymerization of actin with cytochalasin D (CD) constitutively activated ribosomal S6 kinase (RSK) and induced inhibitory phosphorylation of Cdc2 (Tyr 15) in IMR-90 cells. In the presence of an actin defect in IMR-90 cells, activating phosphorylation of Wee1 kinase (Ser 642) and inhibitory phosphorylation of Cdc25C (Ser 216) was also maintained. However, when kinase-dead RSK (DN-RSK) was overexpressed, we observed sustained activation of ERK1/2, but no delay in the G2/M transition, demonstrating that RSK functions downstream of ERK in cell cycle delay by actin dysfunction. In DN-RSK overexpressing IMR-90 cells treated with CD, phosphorylation of Cdc25C (Ser 216) was blocked and phosphorylation of Cdc2 (Tyr 15) was decreased, but the phosphorylation of Wee1 (Ser 642) was maintained, demonstrating that RSK directly controls phosphorylation of Cdc25C (Ser 216), but not the activity of Wee1. These results strongly suggest that actin dysfunction in primary cells activates ERK1/2 to inhibit Cdc2, delaying the cell cycle at G2/M by activating downstream RSK, which phosphorylates and blocks Cdc25C, and by directly activating Wee1.

• The Korean Journal of Physiology and Pharmacology
• /
• 제19권4호
• /
• pp.357-363
• /
• 2015

The purpose of this study was to compare the inhibitory effect of bevacizumab on human Tenon's fibroblasts (HTFs) cultured from primary and recurrent pterygium. Cultured HTFs were exposed to 2.0, 5.0, 7.5, and 15.0 mg/mL concentration of bevacizumab for 24 hours. The 3-[4,5-dimethylthiazol- 2-yl]-2,5-diphenyl tetrazolium bromide and lactate dehydrogenase leakage assays were then performed to assess fibroblast metabolism and viability. The matrix metalloproteinase (MMP), procollagen type I C terminal propeptide (PIP), and laminin immunoassays were performed to examine extracellular matrix production. Changes in cellular morphology were examined by phase-contrast and transmission electron microscopy. Both metabolic activity and viability of primary and recurrent pterygium HTFs were inhibited by bevacizumab in a dose-dependent manner, especially at concentrations greater than 7.5 mg/mL. Both types of HTFs had significant decreases in MMP-1, PIP, and laminin levels. Distinctly, the inhibitory effect of bevacizumab on MMP-1 level related with collagenase in primary pterygium HTFs was significantly higher than that of recurrent pterygium. Significant changes in cellular density and morphology both occurred at bevacizumab concentrations greater than 7.5 mg/mL. Only primary pterygium HTFs had a reduction in cellular density at a bevacizumab concentration of 5.0 mg/mL. Bevacizumab inhibits primary and recurrent pterygium HTFs in a dose-dependent manner, especially at concentrations greater than 7.5 mg/mL. As the primary HTFs produces larger amounts of MMP-1 compared to recurrent HTFs, significant reduction in MMP-1 level in primary pterygium HTFs after exposure to bevacizumab is likely to be related to the faster cellular density changes in primary pterygium HTFs.

• 대한화장품학회지
• /
• 제36권1호
• /
• pp.65-69
• /
• 2010

콜라겐은 포유동물의 가장 풍부한 동물성 단백짙로, 전체 단백질의 약 30 %를 차지하며, 결합 조직에 존재하며 대부분의 장기의 구조적 지지에 기여한다. Tripeptide (glycine-proline-hydroxyproline: INCI name Tripeptide-29) 는 collagen type 1의 주성분이며, palmitoyl tripeptide (palmitoyl-glycine-proline-hydroxyproline: INCI name Palmitoyl Tripeptide-29) 는 콜라겐의 합성을 촉진하는 항노화 불질로서 디자인된 합성소재이다 합성된 웹타이드 유도체는 HPLC를 이용하여 분식하였다. in vitro test를 통하여 콜라겐합성과 섬유아세포 증식 효능을 확인하였고, 비침습적 기기를 사용하여 피검자에 대한 8주간의 적용결과 피부주름과 탄력의 상당한 개선을 확인하였다. Palmitoyl tripeptide는 우수한 항노화 효능을 갖는 화장품 소재로 사료된다.

• 전기전자학회논문지
• /
• 제26권3호
• /
• pp.494-499
• /
• 2022

본 논문에서는 인간의 피부섬유모세포(Human dermal fibroblasts)로부터 확보한 전사체 정보를 활용하여 나이를 예측하는 방법을 소개한다. 제안 방법에서는 훈련을 통해 확보한 분류기 및 회귀 모델을 이용하여 샘플이 속한 적합한 연령 그룹을 선택한 후, 선택된 연령 그룹에 속하는 훈련 데이터의 관측값을 활용하여 구체적인 연령을 예측한다. 연령을 예측하려는 샘플이 입력되면 복수 개의 판별 규칙이 순서대로 실행되는데, 개별 판별 규칙에서는 분류기와 회귀 모델을 동시에 실행하여 해당 판별 규칙에 대한 선택조건이 만족되는지 여부를 확인한다. 선택 조건이 만족될 경우 판별 규칙의 타겟 연령 그룹에 속하는 데이터를 이용하여 훈련된 회귀 모델로 연령을 예측하며, 선택 조건이 만족되지 않으면 후속 판별 규칙을 실행한다. 공개 데이터에 대하여 실험한 결과 기존 연구에서 달성한 7.7년의 평균 예측 오차보다 우수한 5.7년이라는 평균 예측 오차를 달성함을 확인하였다.

• 대한본초학회지
• /
• 제28권1호
• /
• pp.9-14
• /
• 2013

Objectives： Bletillae Rhizoma, the roots of Bletilla striata, is used to restrain the leakage of blood and stop bleeding. It can cure the sores, ulcers, and chapped skin. This study was designed to investigate the collagen metabolism, elastase and tyrosinase activity of Bletillae Rhizoma extract (BR). Methods : The effects of BR on type I procollagen production and collagenase activity in human normal fibroblasts Hs68 after UVB (312 nm) irradiation were measured by ELISA method. The elastase activity, tyrosinase activity, and L-DOPA oxidation after treatment of BR were measured as well. Results : In the present study, the collagen production (type I procollagen) was significantly increased to $15.7{\pm}1.8$ ng/ml at a concentration of BR 100 ${\mu}g/ml$ in UVB damaged Hs68 cells. The increased collagenase activity after UVB damage was significantly recovered to $42.7{\pm}0.7%$, $54.5{\pm}3.5%$, and $38.4{\pm}0.9%$ by BR 10, 30, and 100 ${\mu}g/ml$. The activities of BR 10 mg/ml on tyrosinase activity was significantly reduced to $45.1{\pm}8.4%$ as well. However, there were no significant effects on the elastase activity and the L-DOPA oxidation. Conclusion : BR showed the promoting effects of collagen synthesis and inhibitory effects of collagenase activity in Hs68, human normal fibroblast cells. And these could be thought to have the anti-wrinkle effects and whitening effects in vitro. These results suggest that BR may have potential as an anti-aging ingredient in cosmetic treatment.

• 동의생리병리학회지
• /
• 제36권5호
• /
• pp.175-180
• /
• 2022

The seeds of Trichosanthes kirilowii (STK) used in traditional Oriental medicine for the treatment of dry cough and constipation have diverse pharmacological activities, including hypolipidemic, antioxidant, immunosuppressive, and anticancer effects. However, the effect of STK on angiogenesis has not been studied yet. In this study, we investigated whether the ethanolic extract of STK (ESTK) can regulate the migration and tube formation of human umbilical vein endothelial cells (HUVECs) and explored the underlying mechanism. Results of transwell assay showed that ESTK treatment dose-dependently suppressed the migration of HUVECs. The conditioned medium collected from H1299 human lung cancer cells was used as a chemoattractant. Our observation suggests that ESTK would inhibit the recruitment of endothelial cells into tumors. In addition, ESTK treatment significantly reduced the tube formation of HUVECs. As a molecular mechanism, we found that vascular endothelial growth factor (VEGF)-induced phosphorylation of VEGF receptor 2 (VEGFR2) was completely blocked by ESTK treatment. The expression of angiogenic factors, including VEGFA, fibroblast growth factor 2 (FGF2), angiopoietin, placental growth factor (PGF), platelet derived growth factor (PDGF), angiogenin, and tumor necrosis factor (TNF)-α, was commonly decreased by ESTK treatment in H1299 cells, indicating that ESTK would reduce the production of angiogenic factors from cancer cells. Taken together, our results clearly demonstrated that ESTK exhibited anti-angiogenic effects in HUVECs, which provides another possible mechanism underlying the anticancer activities of STK.

• Biomolecules & Therapeutics
• /
• 제32권2호
• /
• pp.224-230
• /
• 2024

Pinitol (3-O-Methyl-D-chiro-inositol) has been reported to possess insulin-like effects and is known as one of the anti-diabetic agents to improve muscle, liver, and endothelial cells. However, the beneficial effects of pinitol on the skin are not well known. Here, we investigated whether pinitol had effects on human dermal fibroblasts (HDFs), and human dermal equivalents (HDEs) irradiated with ultraviolet A (UVA), which causes various damages including photodamage in the skin. We observed that pinitol enhanced wound healing in UVA-damaged HDFs. We also found that pinitol significantly antagonized the UVA-induced up-regulation of matrix metalloproteinase 1 (MMP1), and the UVA-induced down-regulation of collagen type I and tissue inhibitor of metalloproteinases 1 (TIMP1) in HDEs. Electron microscopy analysis also revealed that pinitol remarkably increased the number of collagen fibrils with regular banding patterns in the dermis of UVA-irradiated human skin equivalents. Pinitol significantly reversed the UVA-induced phosphorylation levels of ERK and JNK but not p38, suggesting that this regulation may be the mechanism underlying the pinitol-mediated effects on UVA-irradiated HDEs. We also observed that pinitol specifically increased Smad3 phosphorylation, which is representative of the TGF-β signaling pathway for collagen synthesis. These data suggest that pinitol exerts several beneficial effects on UVA-induced damaged skin and can be used as a therapeutic agent to improve skin-related diseases.

• 생명과학회지
• /
• 제24권8호
• /
• pp.837-842
• /
• 2014

이 연구의 목적은 사람 폐 섬유아세포인 IMR 90 에서 Brunfelsia grandiflora 에탄올 추출물(BGEE)이 SIRT1 및 p53 활성화를 통해 autophagy의 유도에 대한 효과를 조사한 것이다. BGEE는 $5{\mu}g/ml$ 이상의 농도에서 IMR 90 세포에서 세포독성을 나타내었다. 본 연구에서 처음으로 BGEE가 autophagy를 유도 하는 것이 발견되었다. 또한, BGEE는 $2.5{\mu}g/ml$ 이하에서 Beclin-1 및 $5{\mu}g/ml$ 이상에서 Atg7 의 활성화가 autophagy의 유도에 관여함을 확인하였다. 더욱이 BGEE는 autophagy와 관련된 단백질 발현을 조절하였는데 p53 및 p-p53 단백질 발현이 세포독성이 없는 농도의 BGEE존재하에서 감소되었다. 하였다. 반면에, SIRT1의 발현수준은 세포독성이 없는 농도의 BGEE로 처리된 IMR 90 세포에서 증가되었다. 더욱이 BGEE로 처리된 사람 페 섬유아세포에서 노화 마커의 지표인 SA-${\beta}$-gal staning이 감소되는 것이 관찰되었다. 이상의 발견들은 BGEE는 사람 폐 섬유아세포에서 p53 및 SIRT1의 조절을 통하여 autophagy 및 항노화 유발을 촉진 시키는 것을 시사하고 있다.