• 제목/요약/키워드: Platelet-derived Growth Factor

검색결과 139건 처리시간 0.025초

혈소판유래 성장인자 함유 흡수성 차폐막이 치주조직의 재생에 미치는 영향 (Effects of platelet-derived growth factor loaded bioresorbable membrane on periodontal regeneration)

  • 구영;김정은;한수부;정종평;박윤정;이승진;권영혁
    • Journal of Periodontal and Implant Science
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    • 제27권1호
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    • pp.61-78
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    • 1997
  • PDGF-BB has been recognized as a highly potential growth factor for guided tissue regeneration in periodontal defect. This study carried out histologic and histometric evaluation of $200ng/cm^2$ PDGF-BB loaded bioresorbable membrane made from polyglycolic and polylactic acid. It was tested for its biocompatibility, ability to prevent epithelial downgrowth and amount of periodontal regeneration. Without membrane and PDGF-BB unloaded bioresorbable membrane were used as control. Healthy six beagle dogs were used. Each dog was anesthetized and buccal flaps were reflected in the mandibular and maxillary premolar areas. Buccal alveolar bone between the mesiobuccal and distobuccal line angles was surgically removed on the lower 2nd and 4th premolar in mandible, 2nd premolar in maxilla, to a level 4mm apical to the cementoenamel junction with creating a Class II buccal furcation defect for available space. Care was taken not to remove the root cementum layer and rubber impression materials were placed over each surgically created defect. Flaps were repositioned and sutured. Reconstructive surgery was performed 1 month after defect preparation. PDGF-BB loaded membranes and controls were randomly placed on maxillary 2nd premolars and mandibular 2nd and 4th premolars. Plaque control regimen was instituted with daily brushing with a 0.1% chlorhexidine digluconate during experimental periods. The animals were sacrificed 2 and 5 weeks after surgery and undecalcified specimens were prepared for histologic evaluation. The degree of coronal regrowth of new bone, new cementum and the amonut of new bone areas formed on the defected area of the PDGF-BB loaded membrnae turned superior to without membrane and drug unloaded membrane. Experimental membrane could prevent the epithelial downgrowth irrespective of drug loaded or not and showed good biocompatiblity, These results implicated that PDGF-BB loaded bioresorbable membrane could be highly useful tool for guided tissue regeneration of periodontal defects.

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마우스 만성 췌장염 모델에서 연교(連翹)와 현호색(玄胡索) 단일 추출물 및 추출 혼합물의 보호 효과 (Protective Effects of Individual Extract and Mixture of Forsythia Fructus and Corydalis Tuber on Chronic Pancreatitis in Mice)

  • 신준연;최지원;김동욱;주자기;권빛나;배기상;송호준;박성주
    • 대한본초학회지
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    • 제36권1호
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    • pp.59-66
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    • 2021
  • Objectives : Forsythiae Fructus has been reported to have anti-inflammatory effects in many diseases, and Corydalis Tuber has been used as a pain suppressor in Eastern Asia. However, the protective effects of individual water extract of Forsythiae Fructus (FF) and Corydalis Tuber (CT) and the mixture of FF and CT (FC) on chronic pancreatitis (CP) were not well-investigated. Therefore, we investigated the protective effects of FF, CT, and FC on CP in mice. Methods : To induce CP, cerulein was injected 6 times a day, 4 times a week for 3 weeks. 1 h before the every cerulein injection, 200 mg/kg of FF, CT, or FC was intraperitoneally injected to mice. Histological analysis of pancreas was examined by hematoxylin and eosin stain and collagen deposition was examined by Masson's trichrome stain. Fibrogenic parameters such as α-smooth muscle actin (α-SMA), extracellular matrix (ECM) deposition, and fibrotic cytokines such as transforming growth factor (TGF)-β1 and platelet-derived growth factor (PDGF) were also analyzed by immunofluorescence stain and real-time PCR. Results : Histological damages in pancreas were inhibited by pre-treatment of FF or FC but not CT. α-SMA and ECM in pancreas were inhibited by pre-treatment of CT or FC but not FF. Moreover, the expression of TGF-β1 and PDGF in pancreas were inhibited by FF, CT or FC. Conclusions : Our results suggest that FC have protective effect on CP in mice through inhibition of α-SMA, ECM, TGF-β1 and PDGF in pancreas, and these findings could suggest new clinical strategy for CP.

한국 홍삼 사포닌이 배양중인 치주인대 세포의 성장 및 분화에 미치는 영향 (THE EFFECTS OF KOREAN RED GINSENG SAPONIN ON THE GROWTH AND DIFFERENTIATION OF HUMAN PERIODONTAL LIGAMENT CELL IN CULTURE)

  • 김인구;김정근;이재현
    • Journal of Periodontal and Implant Science
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    • 제25권1호
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    • pp.45-55
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    • 1995
  • 치주질환의 치유에 있어서 치주인대 세포의 증식과 분화는 매우 중요하다. 몇몇 학자들에 의해 치주인대 세포의 증식과 분화에 영향을 주는 platelet derived growth나 fibronectin과 같은 growth factor에 대한 연구가 있었다. 이 연구는 홍삼 총사포닌이 치주인대 세포에 미치는 세포독성과 세포의 성장 및 분화에 미치는 영향을 규명하고자 사람의 치주인대 세포를 분리, 배양하여 실험하였다. 총사포닌이 치주인대 세포에 미치는 세포독성을 특정하기 위해 여러가지 농도의 총사포닌을 세포배양액에 첨가하여 1주일 배양후의 결과와 단일 농도($1{\mu}g/ml$})하에서의 세포 성장을 혈구계산반을 사용하여 관찰하였다. 치주인대 세포가 조골세포양세포로의 분화과정에 사포닌이 영향을 미치는 것을 관찰하기 위해 개개의 총사포닌 농도)0.1,1,$10{\mu}g/ml}$)를 세포배양액에 첨가하여 배양하였다. 치주인대 세포가 조골세포의 표현형으로 분화되는데 미치는 총사포닌의 영향을 알아보기 위하여 총사포닌의 단일 농도($1{\mu}g/ml$)하에서 $50{\mu}g/ml$ ascorbic acid와 10mM ${\beta}-glycerophosphate$를 배양액에 첨가하여 배양후 von Kossa's staining을 시행하여 생성된 골결절을 관찰하였다. 이상의 실험에서 얻어진 결과는 아래와 같다. 1. 각각의 농도를 투여한 결과, $1{\mu}g/ml$의 총사포닌에 의해서 세포독성이 유의성있게 증가하였다. 2. 0.01,0.01,1,$10{\mu}g/ml$의 총사포닌을 세포배양액에 첨가한 다음 7일 후의 고나찰시 cell viability가 실험농도 모두에서 유의성있게 증가하였다. 3. 0.1,1,10,$100{\mu}g/ml$의 농도에서 유외성있는 세포 증식이 있었다. 4. $1{\mu}g/ml$의 총사포닌을 세포배양액에 첨가한 다음 1,3,5,7,9일의 관찰시 시간경과에 따라 유의성있는 세포 증식이 있었다. 5. $10{\mu}g/ml$의 총사포닌을 세포배양액에 첨가시 ALP activity가 대조군에 비해 유외성있게 증가하였다. 6. $1{\mu}g/ml$의 총사포닌으로 배양된 치주인대 세포내에서 ALP positive cell이 관찰되었다. 7. $1{\mu}g/ml$의 총사포닌으로 배양된 치주인대 세포내에서 골결절 형성이 관찰되었다.

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Hydroxyapatite를 이식한 임플란트 주위 골결손부에서 rhPDGF-BB와 rhBMP-2가 골내 임플란트 osseointegration에 미치는 영향: Micro-CT 분석과 조직학적 평가 (EFFECT OF RHPDGF-BB AND RHBMP-2 ON OSSEOINTEGRATION OF TITANIUM IMPLANTS AT PERIIMPLANT BONE DEFECTS GRAFTED WITH HYDROXYAPATITE: MICRO-CT AND HISTOLOGIC ANALYSIS)

  • 박지현;황순정;김명진
    • Maxillofacial Plastic and Reconstructive Surgery
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    • 제31권6호
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    • pp.461-468
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    • 2009
  • Purpose: Platelet derived growth factor(PDGF)-BB and bone morphogenetic protein(BMP)-2 are well-known representative growth factors. The purposes of this study were to investigate the effect of rhPDGFBB and rhBMP-2 on osseointegration of titanium implants at periimplant bone defects grafted with hydroxyapatite and to evaluate the feasibility of imaging bone structures around screw-type titanium implant with micro-CT. Materials and Methods: The first molar and all premolars in the mandible region of four beagle dogs were extracted. Following a healing period of 4 months, three $8{\times}8{\times}6mm$-sized bony defects were formed and screw-type titanium implants were placed with hydroxyapatite(HA) block and growth factors; Control group, PDGF group and BMP group. Two months post-implantation, the mandible was harvested. Bone volume(BV), bone-to-implant contact(BIC) and bone mineral density(BMD) were analyzed with micro-CT and histology. Results: According to micro-CT analysis, BV and BMD measures of PDGF and BMP group were significantly higher than control group(BV; PDGF group: $p{\fallingdotseq}0.011$, BMP group: $p{\fallingdotseq}0.006$/BMD; PDGF group: $p{\fallingdotseq}0.020$, BMP group: $p{\fallingdotseq}0.011$) and BIC measures of BMP group were significantly higher than PDGF group($p{\fallingdotseq}0.015$). In histologic evaluation, BIC measures of BMP group was significantly higher than PDGF group($p{\fallingdotseq}0.048$). The values of BV in histologic sections were higher than in micro-CT images and the values of BIC in micro-CT images were higher than in histologic sections. Conclusion: The findings of this experimental study indicates that the use of rhPDGF-BB and rhBMP-2 can increase new bone formation in a large bony defect around titanium implant, and rhBMP-2 is more effective than rhPDGF-BB. Micro-CT can be considered useful for assessment as a rapid and nondestructive method for 3-dimensional measurement of bone healing around implants. Further study is necessary, however, to remove metal artifacts around titanium implant and to standardize the method.

The Significance of SDF-1α-CXCR4 Axis in in vivo Angiogenic Ability of Human Periodontal Ligament Stem Cells

  • Bae, Yoon-Kyung;Kim, Gee-Hye;Lee, Jae Cheoun;Seo, Byoung-Moo;Joo, Kyeung-Min;Lee, Gene;Nam, Hyun
    • Molecules and Cells
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    • 제40권6호
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    • pp.386-392
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    • 2017
  • Periodontal ligament stem cells (PDLSCs) are multipotent stem cells derived from periodontium and have mesenchymal stem cell (MSC)-like characteristics. Recently, the perivascular region was recognized as the developmental origin of MSCs, which suggests the in vivo angiogenic potential of PDLSCs. In this study, we investigated whether PDLSCs could be a potential source of perivascular cells, which could contribute to in vivo angiogenesis. PDLSCs exhibited typical MSC-like characteristics such as the expression pattern of surface markers (CD29, CD44, CD73, and CD105) and differentiation potentials (osteogenic and adipogenic differentiation). Moreover, PDLSCs expressed perivascular cell markers such as NG2, ${\alpha}-smooth$ muscle actin, platelet-derived growth factor receptor ${\beta}$, and CD146. We conducted an in vivo Matrigel plug assay to confirm the in vivo angiogenic potential of PDLSCs. We could not observe significant vessel-like structures with PDLSCs alone or human umbilical vein endothelial cells (HUVECs) alone at day 7 after injection. However, when PDLSCs and HUVECs were co-injected, there were vessel-like structures containing red blood cells in the lumens, which suggested that anastomosis occurred between newly formed vessels and host circulatory system. To block the $SDF-1{\alpha}$ and CXCR4 axis between PDLSCs and HUVECs, AMD3100, a CXCR4 antagonist, was added into the Matrigel plug. After day 3 and day 7 after injection, there were no significant vessel-like structures. In conclusion, we demonstrated the perivascular characteristics of PDLSCs and their contribution to in vivo angiogenesis, which might imply potential application of PDLSCs into the neovascularization of tissue engineering and vascular diseases.

스트레스-유도 열충격단백질 27(Heat Shock Protein 27)의 활성과 물리치료의 상관성 (The Activation of Stress-induced Heat Shock Protein 27 and the Relationship of Physical Therapy)

  • 김미선;이성호;김일현;황병용;김중환
    • The Journal of Korean Physical Therapy
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    • 제20권1호
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    • pp.57-65
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    • 2008
  • Purpose: Heat shock proteins (HSPs) are a group of proteins that are activated when cells are exposed to a variety of environmental stresses, such as infection, inflammation, exposure to toxins, starvation, hypoxia, brain injury, or water deprivation. The activation of HSPs by environmental stress plays a key role in signal transduction, including cytoprotection, molecular chaperone, anti-apoptotic effect, and anti-aging effects. However, the precise mechanism for the action of small HSPs, such as HSP27 and mitogen-activated protein kinases (MAPKs: extracellular-regulated protein kinase 1/2 (ERK1/2), p38MAPK, stress-activated protein kinase/c-Jun N-terminal kinase (SAPK/JNK), is not completely understood, particularly in application of cell stimulators including platelet-derived growth factor (PDGF), angiotensin II (AngII), tumor necrosis factor $\alpha$ (TNF$\alpha$), and $H_2O_2$. This study examined the relationship between stimulators-induced enzymatic activity of HSP27 and MAPKs from rat smooth and skeletal muscles. Methods: 2-dimensional electrophoresis (2DE) and matrix assisted laser desorption ionizationtime-of-flight/time-of-flight (MALDI-TOF/TOF) analysis were used to identify HSP27 from the intact vascular smooth and skeletal muscles. Three isoforms of HSP27 were detected on silver-stained gels of the whole protein extracts from the rat aortic smooth and skeletal muscle strips. Results: The expression of PDGF, AngII, TNF$\alpha$, and $H_2O_2$-induced activation of HSP27, p38MAPK, ERK1/2, and SAPK/JNK was higher in the smooth muscle cells than the control. SB203580 (30${\mu}$M), a p38MAPK inhibitor, increased the level of HSP27 phosphorylation induced by stimulators in smooth muscle cells. Furthermore, the age-related and starvation-induced activation of HSP27 was higher in skeletal muscle cells (L6 myoblast cell lines) and muscle strips than the control. Conclusion: These results suggest, in part, that the activity of HSP27 and MAPKs affect stressors, such as PDGF, AngII, TNF$\alpha$, $H_2O_2$, and starvation in rat smooth and skeletal muscles. However, more systemic research will be needed into physical therapy, including thermotherapy, electrotherapy, radiotherapy and others.

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Bleomycin 유도 폐 섬유화에 있어서 성장인자 및 Cytokine의 역할 (Role of Growth Factors and Cytokines on Bleomycin Induced Pulmonary Fibrosis)

  • 이용희;정순희;안철민;김성규;조상호
    • Tuberculosis and Respiratory Diseases
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    • 제44권4호
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    • pp.871-888
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    • 1997
  • 연구배경 : 특발성 폐 섬유화확 병인론으로 폐포염과 폐에 침윤한 염증세포 및 폐 조직자체의 실질세포들이 성장인자를 포함한 다양한 cytokine을 분비하여 실질조직을 구성하는 세포에 손상을 야기함으로써 종국에는 섬유화를 초래하는 것으로 이해하고 있다. 그러나 이들에 대한 개괄적인 연구가 부족하고 매개체 각각에 대한 단편적인 논문들뿐이어서 본 연구에서는 BLM유도 폐 손상및 섬유화의 발생기전에 있어서 IL-1, IL-6, TNF-$\alpha$와 TGF-${\beta}_1$, PDGF, bFGF들의 역할을 규명하고자 하였다. 방 법 : Wistar백서를 정상대조군, BLM투여군, BLM과 비타민 E병합투여군으로 나누었고 BLM 투여후 제 1, 2, 3, 4, 5, 7, 14, 21, 28일에 각각 도살한 다음 기관지폐포 세척술을 시행하여 시기별 총 세포수, 세포 구성성분비율을 살펴보았고 TGF-${\beta}_1$, PDGF, bFGF, IL-1, IL-6, TNF-$\alpha$에 대한 면역조직화학 염색, TGF-${\beta}_1$ mRNA에 대한 동소보합결합검사를 시행, 각 매개체의 생성소, 발현분포 및 정도를 분석하였다. 결 과 : BLM 투여후 1~7 일에 중성구와 기관지상피세포에서 생성된 IL-1, IL-6는 폐손상부위로 원하는 것으로 생각되며 7일이내에 기관지상피세포에서의 IL-1, IL-6 의 양성발현은 기관지상피세포가 BLM 유도 폐 섬유화시 기도주변에서 일어나는 염증 및 면역반응을 항진 및 유지시키는 간접증거로 생각된다. TNF-$\alpha$는 BLM투여후 1~5일에는 기관지상피세포, 중성구가 주생성소로 폐손상부위로의 염증세포의 이동에 주요역할을 하는 것으로 생각되며 7~28일에는 대식세포가 주생성소로서 섬유화를 촉진시키는 것으로 생각된다. TGF-${\beta}_1$은 기관지 상피세포, 대식세포가 주생성소로서 섬유모세포가 표적세포로 생각되며 섬유모세포가 세포외 기질을 생성하도록 자극하고 대식세포에서 유리된 PDGF와 함께 섬유모세포의 증식을 자극한다. 대식세포 및 섬유모세포에서 유리된 bFGF는 TGF-${\beta}_1$과 함께 교원질과 같은 세포외기질의 생성을 자극하는 것으로 여겨진다. 비타민 E와 BLM 병합투여군의 경우 6가지 성장인자 및 cytokine의 발현세포는 같았으나 발현세포수는 극히 미미하였고 trichrome염색상 섬유화도 미약하였다. 결 론 : BLM으로 인한 혈관내피 및 폐포상피세포 손상이후 침윤한 중성구 및 기관지 상피세포가 IL-1, IL-6, TNF-$\alpha$를 분비하여 BLM투여 1~7 일에 많은 수의 중성구를 동원하도록 유도하며 이들이 유리하는 다양한 효소 및 산소유리기가 폐의 정상구조를 파괴하여 섬유화를 시작하게 하는 것으로 생각한다. 손상이 진행됨에 따라 BLM투여 7~28 일에 대식세포가 유리하는 TGF-${\beta}_1$, PDGF, bFGF, TNF-$\alpha$는 섬유모세포를 자극, 이들의 증식을 유도하고 또한 세포외기질의 생성증가를 유도하여 폐 섬유화를 진행시키는 것으로 사료되며 TNF-$\alpha$는 BLM투여후 전 기간에 걸쳐 다수의 세포에서 발현된 점으로 미루어 섬유화에 있어서 TGF-${\beta}_1$ 못지않은 중요한 역할을 하는 것으로 여겨진다. 또한 비타민 E가 BLM유도 폐 손상으로 인한 폐 섬유화의 정도를 감소시키는 것으로 생각한다.

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양하 꽃대의 생리활성 및 양갱 제조 (Biological Activity and Manufacturing of Yanggeng with Yangha Flower Buds)

  • 김민주;김애정
    • 한국식품영양과학회지
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    • 제44권8호
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    • pp.1180-1185
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    • 2015
  • 본 연구에서는 폐경 이후 발생률이 높은 심혈관계 질환 예방에 도움을 줄 수 있는 식품을 개발할 목적으로 PDGF-BB로 혈관평활근세포의 이주와 증식을 유도한 다음 양하 꽃대 추출물이 혈관평활근세포의 이주와 증식에 미친 억제 효과를 알아보았다. 그리고 양하 꽃대 시료를 첨가한 양갱을 제조하여 그 품질 특성을 평가, 최적 비율의 양하 꽃대 양갱을 확인하고자 하였다. 혈관평활근세포의 이주에서는 양하 꽃대 추출물 $100{\mu}g/mL$에서부터 정상세포와 유사한 수준을 나타냈다. 또한 증식에서는 양하 꽃대 추출물 $10{\mu}g/mL$에서부터 확연히 억제되어 $1,000{\mu}g/mL$에서는 정상세포 수준까지 떨어졌다. 양하 양갱의 경우 양하 꽃대 시료 첨가량이 높아질수록 명도와 황색도는 유의적(P<0.05)으로 감소한 반면 적색도는 증가하였다. 양하 꽃대를 이용한 양갱의 관능평가 결과를 종합해보면 양하 꽃대 시료 9 g 첨가군(YY9)에서 가장 높은 점수가 나타났다. 양하 꽃대는 항산화 활성 향상과 혈관평활근세포의 이주와 증식을 억제하는 작용이 나타났으므로, 혈관 손상을 예방해줄 수 있는 기능성식품으로서의 가능성을 확인하였다. 따라서 관능평가에서 우수한 점수를 보여준 양하 꽃대 시료 9 g 첨가 양하 양갱은 중년여성의 심혈관질환 예방에 도움을 줄 수 있는 식품으로 기대된다.

In Vivo Angiogenic Capacity of Stem Cells from Human Exfoliated Deciduous Teeth with Human Umbilical Vein Endothelial Cells

  • Kim, Ji-Hye;Kim, Gee-Hye;Kim, Jae-Won;Pyeon, Hee Jang;Lee, Jae Cheoun;Lee, Gene;Nam, Hyun
    • Molecules and Cells
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    • 제39권11호
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    • pp.790-796
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    • 2016
  • Dental pulp is a highly vascularized tissue requiring adequate blood supply for successful regeneration. In this study, we investigated the functional role of stem cells from human exfoliated deciduous teeth (SHEDs) as a perivascular source for in vivo formation of vessel-like structures. Primarily isolated SHEDs showed mesenchymal stem cell (MSC)-like characteristics including the expression of surface antigens and in vitro osteogenic and adipogenic differentiation potentials. Moreover, SHEDs were positive for NG2, ${\alpha}$-smooth muscle actin (SMA), platelet-derived growth factor receptor beta ($PDGFR{\beta}$), and CD146 as pericyte markers. To prove feasibility of SHEDs as perivascular source, SHEDs were transplanted into immunodeficient mouse using Matrigel with or without human umbilical vein endothelial cells (HUVECs). Transplantation of SHEDs alone or HUVECs alone resulted in no formation of vessel-like structures with enough red blood cells. However, when SHEDs and HUVECs were transplanted together, extensive vessel-like structures were formed. The presence of murine erythrocytes within lumens suggested the formation of anastomoses between newly formed vessel-like structures in Matrigel plug and the host circulatory system. To understand underlying mechanisms of in vivo angiogenesis, the expression of angiogenic cytokine and chemokine, their receptors, and MMPs was compared between SHEDs and HUVECs. SHEDs showed higher expression of1VEGF, SDF-$1{\alpha}$, and $PDGFR{\beta}$ than HUVECs. On the contrary, HUVECs showed higher expression of VEGF receptors, CXCR4, and PDGF-BB than SHEDs. This differential expression pattern suggested reciprocal interactions between SHEDs and HUVECs and their involvement during in vivo angiogenesis. In conclusion, SHEDs could be a feasible source of perivascular cells for in vivo angiogenesis.

PDGF와 LPS가 치주 인대 세포의 활성에 미치는 영향에 관한 연구 (The Effects of PDGF and LPS on the Viability of Human Periodontal Ligament Cells)

  • 허정;임정현;김상철
    • 대한치과교정학회지
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    • 제28권1호
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    • pp.143-153
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    • 1998
  • PDGF와 LPS는 골 대사에 중요한 조절요소이다. 외인성 PDGF는 골 흡수를 자극하기도 하고, 또 새로운 골 형성을 자극하기도 한다. LPS는 골파괴 활성의 자극 요인으로 알려져 있다. 본 연구의 목적은 골개조에 중요한 역할을 하는 치주 인대에 PDGF와 LPS의 상호 작용을 평가하기 위해서 시행되었다. 배양된 사람의 치주 인대 세포에 PDGF와 LPS를 첨가 배양하여 각 농도와 시간에 따른 대조군에 대한 백분율로 환산된 세포 활성의 평균과 표준 편차를 구하고 ANOVA를 시행하여 다음과 같은 결과를 얻었다. 1. PDGF를 단독으로 가한 경우 0.1ng/ml에서는 세포 활성이 대조군과 차이가 없었으나 1ng/ml에서는 배양 2일째에, 10ng/ml에서는 배양 2,3일째에 유의한 세포 활성 증가를 보였다. 2. LPS단독처리시 $0.5{\mu}g/ml$$5{\mu}g/ml$농도에서 배양 1일째,2일째에는 대조군과 차이가 없었으나 배양 3일째에 유의한 활성 감소가 없었다. 3. $0.5{\mu}g/ml$$5{\mu}g/ml$농토의 LPS에 1ng/m 및 10ng/ml농도의 PDGF 첨가시, 배양 3일째에 LPS단독 투여시보다 유의한 세포 활성 증가가 있었으며 특히 10ng/ml PDGF 첨가시에는 대조군보다 활성이 컸다. 이상의 연구결과로 골개조 과정에 관여하는 것으로 여겨지는 치주 인대세포에 대한 적절한 농도의 PDGF와 LPS의 복합 투여는 PDGF 단독 투여 못지 않게 치주 인대세포의 활성을 증가시키는 것으로 사료된다.

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