• 제목/요약/키워드: Human Fibroblast

검색결과 799건 처리시간 0.023초

제니스테인에 의한 노화된 피부세포 활성화와 콜라겐 생성 효과 (The Effects of Genistein on the Proliferation and Type I pN Collagen Synthesis in Aged Normal Human Fibroblasts)

  • 양은순;홍란희;강상모
    • 한국미생물·생명공학회지
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    • 제35권4호
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    • pp.316-324
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    • 2007
  • 콩류에 다량 존재하는 제니스틴으로부터 얻을수 있는 제니스테인이 노화된 피부 섬유아세포의 활성과 피부의 주성분인 콜라겐의 합성 및 이의 주요한 분해 효소인 MMP-1의 합성에 어떤 영향을 미치는지 알아보고자 하였다. 제니스테인은 54세의 섬유아세포 증식을 유의하게 증가시켰으며, 이러한 세포증식 효과는 비타민 A와 유사하게 자연노화가 많이 진행된 세포에서 뚜렷하였다. 아울러 77세의 섬유아세포에서 제니스테인 처리에 의해 세포노화의 지표인 SA-${\beta}$-Gal 염색이 감소된 것을 확인하였다. 그리고 제니스테인은 섬유아세포에서 type I pN 콜라겐의 합성을 촉진하였고, UVA에 의해 콜라겐 합성이 매우 억제된 상황에서도 합성 증가 효과를 보였는데 이러한 현상은 자연노화가 많이 진행된 세포에서 더욱 효과적이었다. 콜라겐 매트릭스를 이용한 콜라겐 생합성 결과에서 제니스테인은 광노출부나 비노출 부위에서 얻은 모두의 세포에서 콜라겐 합성을 증가시킴을 알 수 있었으며, 이를 통해 제니스테인이 광노화 및 자연노화에 모두 효과적인 것으로 추측할 수 있다. 제니스테인은 젊은 피부의 세포에서 MMP-1의 합성에는 큰 영향을 미치지 않았으나, 노화된 피부의 세포에서 매우 증가되어 있는 MMP-1의 합성을 억제하였다. 이상의 결과에서 제니스테인은 광노화 뿐 아니라, 자연 노화에 의한 피부 주름을 예방하는데 유용한 물질이 될 것으로 사료된다.

발아콩 및 목련박피 혼합추출물(SeleMix AN)에 의한 여드름 개선 효과 (Improving Effect for Acne with SeleMix AN Composed of Germinating Soy Bean and Magnolia Bark Extract)

  • 류종성;김진황;곽택종;김기선;김진준;이천구;박경찬
    • 대한화장품학회지
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    • 제33권1호
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    • pp.29-32
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    • 2007
  • In vitro 및 in vivo에서 모두 효과를 나타내는 새로운 여드름 개선 성분을 개발하였다. 특히, in vitro에서 효과가 검증된 많은 원료들이 실제 여드름환자에게서 실질적인 효능을 나타내지 못하는 경우가 많아, 본 연구에서는 임상에서 실질적인 효과를 보일 수 있는 원료의 개발에 초점을 맞추었다. 우선적으로 여드름에 효과가 높은 것으로 알려져 있거나 여드름개선 효과가 기대되는 천연물질의 추출물을 대상으로 소규모의 예비임상시험을 통해 효능을 확인하였다. 여러 가지 후보물질 중에서 발아콩과 목련박피 2종의 추출물이 여드름 및 여드름에 의한 홍조현상과 흉터에 뚜렷한 효과를 나타내어 이 두 천연물의 혼합추출물을 SeleMix AN이라 명명하였다. 200여 명의 예비임상시험을 통해서 SeleMix AN의 임상적 효과를 확인한 후 상기 물질의 여드름 개선 작용기작을 규명하기 위한 in vitro 효능테스트를 실시하여 P. Acne 성장억제 효과(시료농도 0.0125%), 16.9%의 히스타민 분비저해효과와 함께, 인간유래 섬유아세포의 활성을 대조군 대비 57% 높여 주는 실험결과를 확인하였다. 최종적으로 분당 서울대병원과의 공동연구를 통해 23명의 여성여드름환자를 대상으로 한 임상평가를 실시하여 새로운 여드름 개선성분의 효능을 검증하였다. 여름에 실시된 최종임상에서 SeleMix AN이 함유된 시료는 피지분비량이 증가하고 여드름 발병율이 높아지는 계절적인 영향에도 불구하고 4주만에 특히, 염증성 병변을 대조군 대비 통계적으로 유의차 있게 감소시키는 뛰어난 여드름 개선 결과를 얻을 수 있었다.

광나무의 주성분, Ursolic acid와 Oleanolic acid의 항노화 효능 (Excellent Anti-aging Effects of Ursolic acid and Oleanolic acid Present in Ligustrum lucidum)

  • 홍용덕;유대성;남미희;김현정;박시준;신송석;천종우;박영호
    • 대한화장품학회지
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    • 제38권2호
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    • pp.181-187
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    • 2012
  • 광나무(L. lucidum)는 ursolic acid와 oleanolic acid를 다량 포함하고 있다. 본 연구에서는 광나무 열매, 줄기, 잎 세 부위 추출물의 항주름 효능을 평가하였다. 광나무 추출물은 human skin fibroblasts에서 독성이 없을 뿐만 아니라 MMP-1과 MMP-2의 발현을 감소시키고 COL1A1의 발현을 증가시켰다. 이들 추출물은 모두 농도 의존적으로 COL1A1의 발현을 증가시켰으며 MMP-1과 MMP-2의 발현을 감소시켰다. 광나무 세 부위 추출물 가운데, 열매 부위에 가장 많은 양의 ursolic acid 와 oleanolic acid가 함유되어 있었으며 가장 강한 COL1A1 upregulating 효과와 MMP-1과 MMP-2 downregulating 효과를 나타냈다. 이처럼 항주름 효능을 보이는 광나무 열매 추출물은 기능성 화장품 소재로 개발될 수 있는 가능성이 있다.

구연산과 테트라싸이클린으로 처리한 치근면에서 rhBMP-2가 치주인대섬유아세포와 골아세포의 활성에 미치는 영향 (Effect of Citric Acid and Tetracycline HCl Root Conditioning on rhBMP-2 on Human Periodontal Ligament Fibroblast and Osteoblast cell)

  • 심정민;한수부;설양조;이용무;김경화;계승범;최상묵;정종평
    • Journal of Periodontal and Implant Science
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    • 제31권1호
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    • pp.21-41
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    • 2001
  • The goal of Periodontal treatment is predictable periodontal regeneration. But until now, many products including GTR materials and growth factors are beyond of complete regeneration. BMP can induce ectopic bone formation when implanted into sites such as rat muscle and can greatly enhance healing of bony defects when applied exogenously. BMP can promote periodontal regeneration by their ability to stimulate new bone and new cementum formation. But little is known about optimal conditions required for the application. Root conditioning is used for bioacive root change so altered root surface provides a substrate that promotes chemotaxis, migration and attachment of peridontal cells encouraging connective attachment to the denuded root surface. The aim of this study is to investigate whether the acid conditioning change effect of rhBMP-2 on human periodontal ligament cell and osteoblast cell line. 288 periodontally involved root dentin slices are divided into 6 groups, each 48, 1)control, 2)treated with BMP, 3)treated with citric acid 4)treated with citric acid+BMP 5)treated with tetracycline 6)treated with TC+BMP. Each group was devided half, so 12 root dentin slices were seeded with periodontal ligament cells and 12 were seeded with osteoblasts. At day 2 and 7, cell number, protein assay, ALP activitiy was measured. To investigate morphology of cultured cells, SEM was employed. Statistical analysis was performed with SPSS 8.0 either t-test or ANOVA test. The results are ; Protein assay and cell number was slightly decreased in CA+BMP group compared to Ca group but it was not statistically significant and ALP activity was much more increased in CA+BMP group compared to CA group so there was no statistically significance between BMP and CA+BMP group and statistically significant compared to control group. Cell number and protein assay was slightly increased in TC group and ALP activity was much less the BMP group and CA group. Cell number and protein and ALP activity was not much increased in TC+BMP group. TC group and TC+BMP group showed cell morphology change in SEM. This results suggested that application of root surface with citric acid before BMP treatment might give better result in periodontal regeneration.

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Inhibition of PKC Epsilon Attenuates Cigarette Smoke Extract-Induced Apoptosis in Human Lung Fibroblasts (MRC-5 Cells)

  • Kang, Shin-Myung;Yoon, Jin-Young;Kim, Yu-Jin;Lee, Sang-Pyo;Jeong, Sung-Hwan;Park, Jeong-Woong
    • Tuberculosis and Respiratory Diseases
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    • 제71권2호
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    • pp.88-96
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    • 2011
  • Background: It is known that cigarette smoke (CS) causes cell death. Apoptotic cell death is involved in the pathogenesis of CS-related lung diseases. Some members of the protein kinase C (PKC) family have roles in cigarette smoke extract (CSE)-induced apoptosis. This study was conducted to investigate the role of PKC epsilon in CSE-induced apoptosis in human lung fibroblast cell line, MRC-5. Methods: Lactate dehydrogenase release was measured using a cytotoxicity detection kit. The MTT assay was used to measure cell viability. Western immunoblot, Hoechst 33342 staining and flow cytometry were used to demonstrate the effect of $PKC{\varepsilon}$. Caspase-3 and caspase-8 activities were determined using a colorimetric assay. To examine $PKC{\varepsilon}$ activation, Western blotting was performed using both fractions of membrane and cytosol. Results: We showed that CSE activated $PKC{\varepsilon}$ by demonstrating increased expression of $PKC{\varepsilon}$ in the plasma membrane fraction. Pre-treatment of $PKC{\varepsilon}$ peptide inhibitor attenuated CSE-induced apoptotic cell death, as demonstrated by the MTT assay (13.03% of control, 85.66% of CSE-treatment, and 53.73% of $PKC{\varepsilon}$ peptide inhibitor-pre-treatment, respectively), Hoechst 33342 staining, and flow cytometry (85.64% of CSE-treatment, 53.73% of $PKC{\varepsilon}$ peptide inhibitor-pre-treatment). Pre-treatment of $PKC{\varepsilon}$ peptide inhibitor reduced caspase-3 expression and attenuated caspase-3, caspase-8 activity compared with CSE treatment alone. Conclusion: $PKC{\varepsilon}$ seem to have pro-apoptotic function and exerts its function through the extrinsic apoptotic pathway in CSE-exposed MRC-5 cells. This study suggests that $PKC{\varepsilon}$ inhibition may be a therapeutic strategy in CS-related lung disease such as chronic obstructive pulmonary disease.

Optimization of growth inducing factors for colony forming and attachment of bone marrow-derived mesenchymal stem cells regarding bioengineering application

  • Quan, Hongxuan;Kim, Seong-Kyun;Heo, Seong-Joo;Koak, Jai-Young;Lee, Joo-Hee
    • The Journal of Advanced Prosthodontics
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    • 제6권5호
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    • pp.379-386
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    • 2014
  • PURPOSE. These days, mesenchymal stem cells (MSCs) have received worldwide attention because of their potentiality in tissue engineering for implant dentistry. The purpose of this study was to evaluate various growth inducing factors in media for improvement of acquisition of bone marrow mesenchymal stem cells (BMMSCs) and colony forming unit-fibroblast (CFU-F). MATERIALS AND METHODS. The mouse BMMSCs were freshly obtained from female C3H mouse femur and tibia. The cells seeded at the density of $10^6$/dish in media supplemented with different density of fetal bovine serum (FBS), $1{\alpha}$, 25-dihydroxyvitamin (VD3) and recombinant human epidermal growth factor (rhEGF). After 14 days, CFU-F assay was conducted to analyze the cell attachment and proliferation, and moreover for VD3, the 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS) assay was additionally conducted. RESULTS. The cell proliferation was increased with the increase of FBS concentration (P<.05). The cell proliferation was highest at the density of 20 ng/mL rhEGF compared with 0 ng/mL and 200 ng/mL rhEGF (P<.05). For VD3, although the colony number was increased with the increase of its concentration, the difference was not statistically significant (P>.05). CONCLUTION. FBS played the main role in cell attachment and growth, and the growth factor like rhEGF played the additional effect. However, VD3 did not have much efficacy compare with the other two factors. Improvement of the conditions could be adopted to acquire more functional MSCs to apply into bony defect around implants easily.

Comparative secretome analysis of human follicular dermal papilla cells and fibroblasts using shotgun proteomics

  • Won, Chong-Hyun;Kwon, Oh-Sang;Kang, Yong-Jung;Yoo, Hyeon-Gyeong;Lee, Dong-Hun;Chung, Jin-Ho;Kim, Kyu-Han;Park, Won-Seok;Park, Nok-Hyun;Cho, Kun;Kwon, Sang-Oh;Choi, Jong-Soon;Eun, Hee-Chul
    • BMB Reports
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    • 제45권4호
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    • pp.253-258
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    • 2012
  • The dermal papilla cells (DPCs) of hair follicles are known to secrete paracrine factors for follicular cells. Shotgun proteomic analysis was performed to compare the expression profiles of the secretomes of human DPCs and dermal fibroblasts (DFs). In this study, the proteins secreted by DPCs and matched DFs were analyzed by 1DE/LTQ FTICR MS/MS, semi-quantitatively determined using emPAI mole percent values and then characterized using protein interaction network analysis. Among the 1,271 and 1,188 proteins identified in DFs and DPCs, respectively, 1,529 were further analyzed using the Ingenuity Pathway Analysis tool. We identified 28 DPC-specific extracellular matrix proteins including transporters (ECM1, A2M), enzymes (LOX, PON2), and peptidases (C3, C1R). The biochemically-validated DPC-specific proteins included thrombospondin 1 (THBS1), an insulin-like growth factor binding protein3 (IGFBP3), and, of particular interest, an integrin beta1 subunit (ITGB1) as a key network core protein. Using the shotgun proteomic technique and network analysis, we selected ITGB1, IGFBP3, and THBS1 as being possible hair-growth modulating protein biomarkers.

헛개나무 분획물에 의한 HDF세포의 초기 노화관련 sm22 단백질 조절 (The Regulation of Early Senescence-related SM22 Protein in Human Dermal Fibroblasts by Hovenia dulcis Thunberg Fractions)

  • 심보람
    • 생명과학회지
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    • 제30권8호
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    • pp.680-687
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    • 2020
  • 본 연구에서는 Hovenia dulcis Thunberg (헛개나무)의 80% 메탄올 분획물의 항산화 및 세포 노화 억제활성을 규명하고자 하였다. 헛개나무 에틸아세테이트 분획물이 DPPH라이칼 소거능에서 가장 높은 활성 저해를 보였고 (RC50 = 3.6±0.8 ㎍/ml), 총 페놀(417.2±5.3 mg GAE/ml) 및 총플라보노이드(260.6±27.5 mg QE/ml) 측정에서도 가장 높은 활성을 보였다. HDF 세포에서 노화가 진행됨에 따라 sm22의 발현이 증가되었고(p<0.001), β-갈락토시다아제의 염색양이 증가(p<0.001)되는 것을 확인하였다. 반면, sm22의 증가는 세포 노화가 진행된 세포일수록 증가폭이 감소되는 것이 확인되었고, 초기노화에서 발현이 높은 것을 알 수 있었다. 헛개나무 에틸아세테이트 분획물을 처리시 HDF세포의 EGF (p<0.01), PDGF-BB (p<0.01), SHH (p<0.05)의 사이토카인이 유의적으로 증가를 보이며, 노화 시 발생된 sm22의 수치를 감소시키는 것을 보였다. 이러한 결과는 헛개나무 에틸아세테이트 분획물이 초기 세포 노화의 작용을 조절할 수 있음을 보여준다.

한방 원료 추출물의 주름개선 효과를 통한 화장품 원료로서의 가치 평가 (The Evaluation of Anti-wrinkle Effects in Oriental Herb Extract)

  • 강금석;김인덕;권륜희;허예영;오상훈;김민아;정혜진;강환열;하배진
    • 생명과학회지
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    • 제17권8호통권88호
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    • pp.1147-1151
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    • 2007
  • 본 연구에서는 7가지 한방원료(음양곽, 복분자, 오미자, 구기자 , 건지황 l 사상자 , 토사자)의 항산화 효과, collagen 합성 촉진 효과, collagenase 활성 저해 효과를 비교 평가함으로써 주름개선 기능성 화장품 원료로서의 사용 가능성을 검토하였다. 항산화 실험인 DPPH 소거 효과, 리놀산 자동산화 억제 효과, superoxide radical 소거 효과, hydroxyl radical 소거 효과에서는 음양곽, 복분자, 오미자, 구기자가 대체적으로 뛰어난 활성을 보여 항노화 화장품 소재로서의 가능성을 보여주었으며, 주름개선 실험인 collagen 합성 촉진 효과, collagenase 저해 효과에서는 건지황, 사상자, 토사자가 다른 네 가지 물질에 비해 뛰어난 효과를 나타내어 주름개선 화장품 소재로서의 가능성을 보여주었다. 이러한 결과는 7가지 한방원료가 항산화 및 주름개선 효능을 나타내므로 기능성 화장품 소재로 활용될 수 있음을 보여 주었다.

Glycosyl flavones from Humulus japonicus suppress MMP-1 production via decreasing oxidative stress in UVB irradiated human dermal fibroblasts

  • Nam, Eui Jeong;Yoo, Gyhye;Lee, Joo Young;Kim, Myungsuk;Jhin, Changho;Son, Yang-Ju;Kim, Sun Young;Jung, Sang Hoon;Nho, Chu Won
    • BMB Reports
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    • 제53권7호
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    • pp.379-384
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    • 2020
  • Exposure to Ultraviolet (UV) light induces photoaging of skin, leading to wrinkles and sunburn. The perennial herb Humulus japonicus, widely distributed in Asia, is known to have anti-inflammatory, antimicrobial, and antioxidant effects. However, the physiological activities of isolated compounds from H. japonicus have rarely been investigated. This study focused on the isolation of active compounds from H. japonicus and the evaluation of their effects on photoaging in UVB-irradiated human fibroblast (Hs68) cells. When the extract and four fractions of H. japonicus were treated respectively in UVB-irradiated Hs68 cells to investigate anti-photoaging effects, the ethyl acetate (EtOAc) fraction showed the strongest inhibitory effect on MMP1 secretion. From EtOAc fraction, we isolated luteolin-8-C-glucoside (1), apigenin-8-C-glucoside (2), and luteolin-7-O-glucoside (3). These compounds suppressed UVB-induced MMP-1 production by inhibiting the phosphorylation of the mitogen-activated protein kinases (MAPKs) and activator protein-1 (AP-1). When the antioxidant activity of the compounds were estimated by conducting western blot, calculating the bond dissociation energies of the O-H bond (BDE) at different grade, and measuring radical scavenging activity, we found luteolin-8-C-glucoside (1) showed the strongest activity on the suppression of UVB-induced photoaging. These results demonstrate the inhibitory effect of three flavone glycosides derived from H. japonicus on MMP-1 production, MAPK and AP-1 signaling, and oxidative stress; this could prove useful in suppressing UVB induced photoaging.