• 제목/요약/키워드: osteoblastic

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적송잎 추출물이 조골세포의 collagen 합성에 미치는 영향 (Effect of Pine (Pinus densiflora) Needle Extracts on Synthesis of Collagen in Osteoblastic MC3T3-E1 Cells)

  • 전민희;김영경;박용수;황현정;김성구;이상현;최인순;김미향
    • 생명과학회지
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    • 제20권4호
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    • pp.607-613
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    • 2010
  • 솔잎은 항산화력이 우수한 것으로 알려져 있으며, mouse calvaria 유래의 MC3T3-E1 osteoblastic cell은 골세포의 세포 활성과 관련된 연구에서 유용하게 이용되어왔다. 따라서 본 연구에서는 MC3T3-E1 세포를 이용하여 적송잎 용매별 추출물이 세포 증식에 미치는 영향과 ALP 활성 및 조골세포의 골 형성을 위한 필수 인자인 콜라겐 합성의 영향에 대해 검토하였다. 적송잎 추출물의 농도(1, 10 50, $100\;{\mu}g/ml$)에 따른 조골세포 성장에 미치는 영향을 MTT assay로 분석한 결과, proanthocyanidin의 경우 $50\;{\mu}g/ml$ 이상 첨가한 군에서 대조군보다 급격한 증식률을 나타내었다. 에탄올 추출물을 첨가하였을 때 유의적인 증식률이 나타나지 않은 반면, 적송잎 헥산 추출물 처리군에 있어서는 $10\;{\mu}g/ml$ 농도 이상에서 유의적으로 세포증식이 촉진되었다. 적송잎 추출물이 ALP 활성에 미치는 영향을 조사한 결과, 적송잎 추출물이 조골세포의 ALP의 활성을 증가시켜 조골세포의 분화에 영향을 줄 가능성이 제시 되었다. 또한 적송잎의 열수 및 에탄올 추출물보다 헥산 추출물에서 조골세포의 ALP 활성이 증가하여 적송잎의 ALP 활성에 영향을 주는 성분은 수용성 성분보다 지용성 성분인 것으로 추측되었다. 적송잎 추출물이 조골세포의 콜라겐 합성에 미치는 실험결과에서 헥산 추출물뿐만 아니라 열수 추출물에서도 높은 콜라겐 합성능력을 나타내었다. 따라서 단일성분에 의한 것보다 복합적 성분들의 상승작용에 의해 조골세포의 콜라겐 합성이 촉진된 것으로 추측할 수 있다. 적송잎 추출물이 조골세포의 증식, ALP 활성 및 콜라겐 합성을 촉진하여 골 생성에 영향을 줄 수 있는 것이 확인되었으며, 그에 대한 구체적인 기작 연구를 위하여 향후 분자생물학적인 차원에서의 in vitro 및 in vivo 실험을 통한 구체적인 연구가 수행되어야 할 것으로 사료된다.

배양된 인간 골막기원세포의 조골세포 분화과정에서 골기질 형성정도와 혈관내피세포성장인자 신호와의 상관관계 (CORRELATION BETWEEN VASCULAR ENDOTHELIAL GRWOTH FACTOR SIGNALING AND MINERALIZATION DURING OSTEOBLASTIC DIFFERENTIATION OF CULTURED HUMAN PERIOSTEAL-DERIVED CELLS)

  • 박봉욱;변준호;류영모;하영술;김덕룡;조영철;성일용;김종렬
    • Maxillofacial Plastic and Reconstructive Surgery
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    • 제29권3호
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    • pp.197-205
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    • 2007
  • Angiogenesis is a essential part for bone formation and bone fracture healing. Vascular endothelial growth factor (VEGF), one of the most important molecules among many angiogenic factors, is a specific mitogen for vascular endothelial cells. VEGF-mediated angiogenesis is required for bone formation and repair. However, the effect of VEGF on osteoblastic cells during osteogenesis is still controversial. In recent days, substantial progress have been made toward developing tissue-engineered alternatives to autologous bone grafting for maxillofacial bony defects. Periosteum has received considerable interest as a better source of adult stem cells. Periosteum has the advantage of easy harvest and contains various cell types and progenitor cells that are able to differentiate into a several mesenchymal lineages, including bone. Several studies have reported the bone formation potential of periosteal cells, however, the correlation between VEGF signaling and cultured human periosteal cell-derived osteogenesis has not been fully investigated yet. The purpose of this study was to examine the correlation between VEGF signaling and cultured human periosteal-derived cells osteogenesis. Periosteal tissues of $5\;{\times}\;20\;mm$ were obtained from mandible during surgical extraction of lower impacted third molar from 3 patients. Periosteal-derived cells were introduced into the cell culture and were subcultured once they reached confluence. After passage 3, the periosteal-derived cells were further cultured for 42 days in an osteogenic inductive culture medium containing dexamethasone, ascorbic acid, and ${\beta}-glycerophosphate$. We evaluated the alkaline phosphatase (ALP) activity, the expression of Runx2 and VEGF, alizarin red S staining, and the quantification of osteocalcin and VEGF secretion in the periosteal-derived cells. The ALP activity increased rapidly up to day 14, followed by decrease in activity to day 35. Runx2 was expressed strongly at day 7, followed by decreased expression at day 14, and its expression was not observed thereafter. Both VEGF 165 and VEGF 121 were expressed strongly at day 35 and 42 of culture, particularly during the later stages of differentiation. Alizarin red S-positive nodules were first observed on day 14 and then increased in number during the entire culture period. Osteocalcin and VEGF were first detected in the culture medium on day 14, and their levels increased thereafter in a time-dependent manner. These results suggest that VEGF secretion from cultured human periosteal-derived cells increases along with mineralization process of the extracellular matrix. The level of VEGF secretion from periosteal-derived cells might depend on the extent of osteoblastic differentiation.

톳 분획물이 조골세포의 증식 및 분화에 미치는 영향 (Effect of Hijikia fusiforme Fractions on Proliferation and Differentiation in Osteoblastic MC3T3-E1 Cells)

  • 전민희;김미향
    • 생명과학회지
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    • 제21권2호
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    • pp.300-308
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    • 2011
  • 톳은 새로운 생리활성 물질을 생산할 수 있는 소재로 각광받고 있으며, mouse calvaria 유래의 MC3T3-E1 세포는 골세포의 세포 활성과 관련된 연구에서 유용하게 이용되어 왔다. 따라서 본 연구에서는 MC3T3-E1 세포를 이용하여 톳 분획물이 세포 증식에 미치는 영향과 ALP 활성, 조골세포의 골 형성을 위한 필수 인자인 collagen 합성 및 조골세포의 표식인자인 골 석회화 형성능에 미치는 영향에 대해 검토하였다. 각 분획물의 수율은 aqueous 분획물이 47.4%로 가장 높은 수율을 나타내었으며 다음으로 butanol 분획물, methanol 분획물 순으로 나타났으며, hexane 분획물이 4.7%로 가장 낮은 수율을 나타내어 극성 성분의 함유량이 더 높은 것으로 확인되었다. 톳분획물의 농도(1, 10 50, 100 ${\mu}g$/ml)에 따른 조골세포 성장에 미치는 영향을 MTT assay로 분석한 결과, 모든 분획물에서 대조군과 비교하여 120% 정도의 증식률을 나타내었다. 이는 선행연구자에 의한 대두 에탄올 추출물 실험 결과인 최고 117%의 세포 증식률과 비슷한 조골세포 증식유도 결과임을 확인할 수 있었다. 톳 분획물이 ALP 활성에 미치는 영향을 조사한 결과, 톳 분획물 중 hexane 분획물과 butanol 분획물이 조골세포의 ALP 활성을 증가시켰으며, 특히 butanol 분획물은 120% 이상의 ALP 활성을 증가시켜 조골세포의 분화에 영향을 줄 가능성이 제시 되었다. 톳 분획물이 조골세포의 collagen 합성에 미치는 실험결과에서 모든 분획물에서 유의적인 collagen 합성능력을 나타내었다. 또한 조골세포의 골 석회화 형성에 미치는 영향은 methanol 분획물을 제외한 다른 분획물에서 유의적인 형성능을 보였으며, 특히 butanol 분획물을 100 ${\mu}g$/ml 첨가하였을 때는 281.25%, aqueous 분획물을 100 ${\mu}g$/ml 첨가하였을 때는 240.46%로 높은 골 석회화 형성능을 나타냈다. 따라서 톳 분획물이 조골세포의 증식, ALP 활성, collagen 합성 및 골 석회화 형성을 촉진하여 골 생성에 영향을 줄 수 있는 것이 확인되었으며, 구체적인 기작 연구와 in vivo 연구가 병행된다면 골다공증 예방과 관련된 기능성 식품의 천연소재로 개발이 가능하리라 사료된다.

Mynol cement에 대한 치근단주위조직 반응에 관한 연구 (Periapical Tissue Reactions to Root Canal Filling with Mynol Cement)

  • 박상진
    • 대한치과의사협회지
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    • 제21권2호통권165호
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    • pp.167-172
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    • 1983
  • This study was to investigate the effects of mynol cement on the periapical tissues of 40 molars in ten dogs. Root canal fillings were placed with mynol cement and the animals were killed at different post operative periods ranging from 1 to 5 weeks. The teeth examined on the basis of microscipic findings. The following results may be drawn; 1. 1 week after root canal fillings, the necrosis of cementum and dentin including alveolar bone was to be seen. There were severe inflammatory changes in the periodontal ligament. 2. 2 weeks after root canal fillings, edematous changes and fibrosis in the periodontal ligament were revealed. 3. After 3-4 weeks, fibrosis was more prominent than 2 weeks. 4. 5 weeks after root canal fillings, the osteoblastic activity was found abundantly surrounding the alveolar bone.

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Mesenchymal stem cells and osteogenesis

  • Jung, Cho-Rok;Kiran, Kondabagil R.;Kwon, Byoung S.
    • IMMUNE NETWORK
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    • 제1권3호
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    • pp.179-186
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    • 2001
  • Bone marrow stroma is a complex tissue encompassing a number of cell types and supports hematopiesis, differentiation of erythreid, nyel and lymphoid lineages, and also maintains undifferentiated hematopoietic stem cells. Marrow-derived stem cells were composed of two populations, namely, hematopoietic stem cells that can differentiate into blood elements and mesenchymal stem cells that can give rise to connective tissues such as bone, cartilage, muscle, tendon, adipose and stroma. Differentiation requires environmental factors and unique intracellular signaling. For example, $TGF-{\beta}$ or BMP2 induces osteoblastic differentiation of mesenchymal stem are very exciting. However, the intrinsic controls involved in differentiation of stem cells are yet to be understood properly in order to exploit the same. This review presents an overview of the recent developments made in mesenchymal stem cell research with respect to osteogenesis.

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우슬 추출물이 골아세포 증식과 분화에 미치는 효과 (Effects of Radix Achyranthis Bidentatae Extract on Proliferation and Differentiation in Human Osteoblast-like Cells)

  • 서은아;문형철
    • 동의생리병리학회지
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    • 제18권6호
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    • pp.1821-1824
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    • 2004
  • In order to investigate the effects of Radix Achyranthis Bidentatae (RAB) on the growth and differentiation of human osteoblast-like cells, we supplemented the culture medium of MG-63 cells with various concentrations of RAB water extracts. RAB extracts significantly stimulated cell growth, as confirmed by the colorimetric MTT (3-dimethylthiazol-2,5-diphenyltetrazolium bromide) assay. RAB extracts also increased the alkaline phosphatase (ALP) activity, which is a osteoblast differentiation marker. These results suggest that RAB can stimulate osteoblastic activity and may represent new pharmacological tools for the treatment of osteoporosis.

슬관절 주위 거대세포종의 치료 (Surgical treatment of Giant Cell Tumor in Knee Joint)

  • 배대경
    • 대한골관절종양학회지
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    • 제1권1호
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    • pp.1-6
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    • 1995
  • Giant cell tumors are primary bone tumors originating from non-osteoblastic connective tissue. The sites of involvement were commonly distal femur, proximal tibia, proximal humerus, distal radius and others (including os calcis, ilium and sacrum). Giant cell tumor located around knee joint has been difficult to treat because of local recurrence following curettage with or without bone graft. Although primary resections reduce recurrence of the lesion, the joint function will be markedly impaired. Marginal excision was very often complicated by a loss of joint integrity since all the giant cell tumors occupy juxtaarticular positions. Techniques involving physical adjuncts(high speed burr and electric cauterization) have been used in the hope of decreasing the rate of local recurrence and avoiding the morbidity of primary resection. A meticulous clinical, radiological and histological evaluation is needed to choose the correct treatment, keeping in mind the possibility of recurrence after each treatment modality.

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근관충전제가 치근단위조직에 미치는 영향에 관한 실험적 연구

  • 최호영
    • 대한치과의사협회지
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    • 제18권9호통권136호
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    • pp.739-745
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    • 1980
  • The histologic responses of periapical tissues to root canal fillings with Grossman sealer were studied 10 dogs. Root canal fillings were performed on the 20 lower and upper teeth. The animals were sacrificed 1,2,3,4 and 5 weeks after the completion of operation. The following results were based on histopathologic studies; 1) After 1 week, the necrosis of dentin and cementum surrounding root apex was found in the root canal fillings. 2) After 2 weeks, the necrosis of cementum and surrounding alveolar bone were revealed. The resorption of dentin was appeared partially. 3) After 2 weeks, newly formed dentin was appeared surrounding necrotic dentin. 4) After 4-5 weeks, the osteoblastic activity was revealed abundantly surrounding the alveolar bone. 5) Fibrosis was prominantly appeared surrounding over-filled area, and fibrous encapsulation was performed.

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