• 제목/요약/키워드: Alizarin red

검색결과 135건 처리시간 0.034초

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.

보생탕이 랫드의 모체와 태자에 미치는 영향에 대한 연구 (Effects of Bosaengtang Administration in Pregnant Rats and Fetuses)

  • 김창석;이선동;김판기;이장우;박해모
    • 대한예방한의학회지
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    • 제9권2호
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    • pp.59-75
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    • 2005
  • 한약은 오랫동안 사용하면서 경험적으로 안전성에 대한 검증이 이루어졌다고 생각하여 독성 문제에 관한 문제가 없는 것으로 판단되고 있다. 하지만, 최근 천연물의 성분들 중 변이원성, 염색체이상에 관한 문제점이 지적되어오고 있다. 특히 최근 임신중의 환경인자나, 약물복용에 따른 기형아 출산원인에 대한 연구가 행하여지고 있는데 임신 초기에 한약을 복용한 경우 기형아 발생률이 높았다는 보고가 있어 한약재의 임신중 사용의 안전성에 대한 과학적 조명이 필요한 실정이다. 임신과 분만에 관련된 한약재는 많이 보고되어 있고 실제로 환자에게 처방되고 있지만 이를 과학적으로 입증하고자 하는 연구는 많지 않았다. 따라서 본 실험은 임신유지, 성장 및 분만과 태아발생 및 그 영향과 관련된 한약재의 효능을 임신 랫드를 이용하여 간접적으로 확인하였다. 우선 임신 랫드를 임신 1일부터 20일까지 보생탕을 경구 투여하여 모체의 체중변화를 살펴보았다. 그리고 임신 20일에 부검하여 채혈을 하여 혈액분석을 하고 모체의 각 장기를 관찰하였다. 또 모체의 자궁을 적출하여 태자를 관찰하였다. 태자는 체중과 외형적 기형 그리고 alcian blue용액과 alizarin red S용액으로 염색하여 골격기형을 관찰하였다. 위와 같은 실험으로 다음과 같은 결과를 얻었다. 보생탕을 투여한 모체의 체중변화에서는 대조군보다 보생탕 투여군이 높은 증가율을 보였지만 전체적으로 두 군 모두 증가현상을 보였으므로 한약에 의한 체중 감소는 없는 것으로 사료되었다. 모체의 장기무게에서 절대중량은 대조군과 보생탕 투여군이 비슷한 결과가 나타났으며 상대중량은 간과 신장에서는 보생탕 투여군이 비장에서는 대조군이 높은 결과가 나타났으나 큰 차이가 나지 않았고 유의성도 나타나지 않았다. 혈액분석결과 백혈구, 적혈구 및 적혈구 관련지표 (MCV, MCH, MCHC), 헤모글로빈, 혈소판, 림프구, 중성구, 호산구, 호염기구, 단핵구등에서는 유의적인 차이가 나지 않았고, 모두 정상범위 이내에 속하였다. AST, ALT, BUN, Creatinine에서도 역시 큰 차이는 없었다. 이것도 역시 모두 정상범위였다. 모체의 황체수, 착상수, 착상율, 임신율, 초기소실율, 후기소실율, 출산자 수, 출산자의 성비를 보면 대조군보다 보생탕 투여군에서 약간 높은 결과를 보였으나 큰 차이는 없었다. 그리고 특히 초기소실율에서는 대조군보다 보생탕 투여군이 높은 결과를 보였다는 점에서 보생탕이 착상이나 임신유지에 유용한 영향이 있었다는 것을 볼 수 있었다. 태자에 대한 영향을 살펴본 결과 태자의 체중과 태자 수는 약간 증가한 것을 볼 수 있었으나 큰 차이는 나지 않았다. 그리고 태자 기형발생에서는 외형적인 기형은 관찰되지 않았고 골격검사에서도 관찰되지 않았다. 그러나 흉추와 흉골에서 변이가 다수 관찰되었다. 흉추에서는 대조군이 흉골에서는 보생탕 투여군이 약간씩 높았으나 대조군과 보생탕 투여군간의 변이는 큰 차이는 없었다. 그리고 천골과 미추에서는 수의 차이가 관찰되었으나 큰 차이는 없었고 미추에서는 유의성이 나타났다.(P<0.01) 그리고 늑골과 경추, 흉추, 요추는 그 수가 일정했다. 이상에서 보생탕 투여는 임신 모체와 태자의 체중 및 증체량의 증가를 촉진시키는 것으로 관찰되었으나, 기타 다른 모체 기능에 관한 지표, 즉 황체수, 착상수, 착상율, 임신율, 초기소실율, 후기소실율등에 영향을 주지 않는 점과 차세대 동물에 대한 검사에서 이상 소견이 관찰되지 않은 점으로 미루어 보생탕 투여는 랫드의 모체와 태자에 독성을 나타내지 않는 것으로 생각된다. 본 연구는 이러한 임신 중 한약의 안전성을 입증하는 연구 결과이며, 향후에도 이상의 결과와 국제 적 연구 경향을 참고하여 임신 중 한약의 안정성과 효과의 입증을 위한 지속적인 실험연구와 임상 보고들이 이루어져야 할 것으로 여겨진다.

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한약재 추출물의 에스트로겐 유사활성 및 조골세포 증식과 분화에 미치는 영향 (The Effects of Medicinal Herbs Extracts on Estrogen-like Activities and Osteoblast Proliferation and Differentiation)

  • 김미향;김보경;김재덕;강아람;이창은;서정민;이동근;조정권;김육용;유기환;이상현
    • 생명과학회지
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    • 제27권4호
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    • pp.456-463
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    • 2017
  • 본 연구는 3종의 한약재(감초(Glycyrrhizae radix), 황기(Astragali radix) 및 산약(Dioscorea rhizome)) 추출물의 에스트로겐 유사활성 및 조골세포 증식과 분화에 미치는 영향을 검토하고자 실험을 진행하였다. 에스트로겐 유사활성 측정을 위하여 인체 유방암 세포주인 MCF7 세포를 luciferase 유전자를 리포터로 사용하는 에스트로겐 반응성 리포터 시스템을 가지는 세포로 형질전환하여 사용하였다. 상기 세포를 이용하여 추출물의 에스트로겐 유사활성을 측정한 결과, 한약재 추출물이 음성대조군과 비교하여 1.11배~5.73배 높은 에스트로겐 유사활성을 나타내었다. 그 중 감초 추출물이 가장 높은 에스트로겐 유사활성을 보였다. 감초 추출물의 에스트로겐 유사활성은 추출물의 농도가 $50{\mu}g/ml$$500{\mu}g/ml$ 일 때 각각 $10^{-8}M$$10^{-7}M$ $17{\beta}-estradiol$과 거의 유사한 활성을 나타내었다. 조골세포주인 MC3T3-E1 세포를 이용한 실험에서는 감초 추출물의 농도가 $1{\sim}1,000{\mu}g/ml$ 범위일 때 독성을 나타내지 않았다. 황기 추출물은 조골세포에 있어서 유의적인 세포 증식률을 보이지 않았다. 그러나, 감초 및 산약 추출물은 각각 148% 및 133%의 최대 증식률을 보였다. 또한, 감초 추출물은 대조군과 비교하여 alkaline phosphatase(ALP) 활성이 증가하였으며, 추출물의 농도가 $100{\mu}g/ml$ 일 때 최대 122%의 ALP 활성을 나타내었다. 또한, Alizarin red S 염색법을 이용한 석회화 형성능 측정에서도 대조군과 비교하여 석회화가 증가하였다. 이러한 결과로 미루어 보아 감초 추출물이 골 형성 및 골다공증 예방 효과가 우수한 식품 소재인 것으로 사료된다.

미역취(Solidago virga-aurea var. gigantea Miq.) 뿌리 추출물이 MC3T3-E1 조골세포의 활성과 분화에 미치는 영향 (Effects of Solidago virga-aurea var. gigantea Miq. Root Extracts on the Activity and Differentiation of MC3T3- E1 Osteoblastic Cell)

  • 박정현;이지원;김현정;이인선
    • 한국식품영양과학회지
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    • 제34권7호
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    • pp.929-936
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    • 2005
  • 골조직은 골아세포, 파골세포, 골세포 등으로 구성되며, 골개조시 여러 인자가 세포증식, 분화, 활성화 및 골대사 조절에 관여한다. 이 때 조골세포의 활성은 골형 성 에 중요하므로, 본 연구에서는 MC3T3-E1 조골세포주를 이용하여 식용자원인 미역취뿌리의 조골세포의 증식과 분화활성에 미치는 영향을 조사하였다. 미역취뿌리 메탄을 추출물 및 분획물이 조골세포의 성장에 미치는 영향을 MTT검색법으로 조사한 결과, 미 역 취 뿌리 메탄을 추출물 10, 100${\mu}g/mL$ 처리시 대조군과 비교하여 각각 140, $120\%$ 증가하여 조골세포의 높은 성장률을 보였다. 미역취 뿌리 추출물 및 순차 분획물 시료가 ALP 효소 활성에 미치는 영향을 3일 간격으로 배지교환 및 시료처 리를 하면서 27일 동안 배양시간에 따른 변화를 측정하여 조사하였다 그 결과, 농도 1, 10, 100${\mu}g/mL$ 처리시 n-hexane과 chloroform분획을 제외한 나머지 분획물들이 시간이 지남에 따라 약간의 ALP활성을 증가시켰고, 메탄올 추출물은 27일째에 대조군에 비해 약 4.4배 이상, 양성 대조군에 비해 약 2배 이상 ALP 활성을 증가시켰다. 미 역취뿌리 메탄올추출물은 다시 ALP효소 염색법과 alizarin red 염색으로 조골세포의 ALP활성유도, 분화와 석회화 형성능을 재확인하였다. 따라서 미역취뿌리 추출물중 골세포의 활성을 촉진시키는 물질은 극성 에 따른 분획물보다 mothanol추출물에서 활성이 높게 나타나는 결과로 미뤄볼 때, 단일성 분에 의한 것보다 복합적 성분들의 상승 작용에 의하여 조골세포의 증식과 분화를 증진시킬 수 있다고 할 수 있다. 아울러 종래의 골질환에 좋다고 알려 진 식품과 양성 대조군에 비해 빠르게 유도하고 있어 앞으로 미역취뿌리에 대한 분자생물학 수준 등의 구체적인 연구들과 기작연구가 지속적으로 이루어져야 할 것이다.

Comparative study on the cellular activities of osteoblast-like cells and new bone formation of anorganic bone mineral coated with tetra-cell adhesion molecules and synthetic cell binding peptide

  • Yu, Hyeon-Seok;Noh, Woo-Chang;Park, Jin-Woo;Lee, Jae-Mok;Yang, Dong-Jun;Park, Kwang-Bum;Suh, Jo-Young
    • Journal of Periodontal and Implant Science
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    • 제41권6호
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    • pp.293-301
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    • 2011
  • Purpose: We have previously reported that tetra-cell adhesion molecule (T-CAM) markedly enhanced the differentiation of osteoblast-like cells grown on anorganic bone mineral (ABM). T-CAM comprises recombinant peptides containing the Arg- Gly-Asp (RGD) sequence in the tenth type III domain, Pro-His-Ser-Arg-Asn (PHSRN) sequence in the ninth type III domain of fibronectin (FN), and the Glu-Pro-Asp-Ilu-Met (EPDIM) and Tyr-His (YH) sequence in the fourth fas-1 domain of ${\beta}$ig-h3. Therefore, the purpose of this study was to evaluate the cellular activity of osteoblast-like cells and the new bone formation on ABM coated with T-CAM, while comparing the results with those of synthetic cell binding peptide (PepGen P-15). Methods: To analyze the cell viability, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay was performed, andto analyze gene expression, northernblot was performed. Mineral nodule formations were evaluated using alizarin red stain. The new bone formations of each group were evaluated using histologic observation and histomorphometrc analysis. Results: Expression of alkaline phosphatase mRNA was similar in all groups on days 10 and 20. The highest expression of osteopontin mRNA was observed in the group cultured with ABM/P-15, followed by those with ABM/T-CAM and ABM on days 20 and 30. Little difference was seen in the level of expression of collagen type I mRNA on the ABM, ABM/T-CAM, and ABM/P-15 cultured on day 20. There were similar growth and proliferation patterns for the ABM/T-CAM and ABM/P-15. The halo of red stain consistent with $Ca^{2+}$ deposition was wider and denser around ABM/T-CAM and ABM/P-15 particles than around the ABM particles. The ABM/T-CAM group seemed to have bone forming bioactivity similar to that of ABM/P-15. A complete bony bridge was seen in two thirds of the defects in the ABM/T-CAM and ABM/P-15 groups. Conclusions: ABM/T-CAM, which seemed to have bone forming bioactivity similar to ABM/P-15, was considered to serve as effective tissue-engineered bone graft material.

임플란트의 표면처리 유형에 따른 골 치유 양상 (Bone Healing around Screw - shaped Titanium Implants with Three Different Surface Topographies)

  • 고영한;김영준;정현주
    • Journal of Periodontal and Implant Science
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    • 제31권1호
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    • pp.41-57
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    • 2001
  • It is well known that the apposition of bone at implant surface would be influenced by the microstructure of titanium implants. The purpose of this study was to compare bone healing around the screw-shaped titanium implant with three different surface topographies in the canine mandibles by histological and biomechanical evaluation. All mandibular premolars of six mongrel dogs were extracted and implants were placed one month later. The pure titanium implants had different surface topographies: smooth and machined ($Steri-OSS^{(R)}$: Group II); sandblasted and acid-etched ($ITI^{(R)}$, SLA: Group III) surface. The fluorescent dyes were injected on the 2nd (calcein), 4th (oxytetracycline HCI) and 12th (alizarin red) weeks of healing. Dogs were sacrificed at 4 and 12 weeks after implantation. The decalcified and undecalcified specimens were prepared for histological and histo-metrical evaluation of implant-bone contact. Some specimens at 12 weeks after implantation were used for removal torque testing. Histologically, direct bone apposition to implant surface was found in all of the treated groups. More mature and dense bone was observed at the implant-bone interface at 12 weeks than that at 4 weeks after implantation. Under the fluorescent microscope, thick regular green fluorescent lines which mean early bone apposition were observed at the implant-bone interface in Group III, while yellow and red fluorescent areas were found at the implant-bone interface in Group I and II. The average implant-bone contact ratios at 4 weeks of healing were 54.3% in Group I, 57.7% in Group II and 66.2% in Group III. In Group I, implant-bone contact ratio was significantly lower than Group II and III(p<0.05). The average implant-to-bone contact ratios at 12 weeks after implantation were 64.3% in Group I, 66.7% in Group II and 71.2% in Group III. There was no significant difference among the three groups. In Group I and II, the implant-bone contact ratio at 12 weeks increased significantly in comparison to ratio at 4 weeks(p<0.05). The removal torque values at 12 weeks after implantation were 90.9 Ncm in Group I, 81.6 Ncm in Group II and 77.1 Ncm in Group III, which were significantly different(p<0.05). These results suggest that bone healing begin earlier and be better around the surface-treated implants compared to the smooth surface implants. The sandblasted and acid-etched implants showed the most favorable bone response among the three groups during the early healing stage and could reduce the waiting period prior to implant loading.

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사람 연골하골 중간엽 줄기세포의 효율적인 골형성 유도 (Induction of Effective Osteogenesis by Mesenchymal Stem Cells from the Human Subchondral Bone)

  • 허정은;조윤제;유명철;백용현;이재동;최도영;박동석
    • Journal of Acupuncture Research
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    • 제23권5호
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    • pp.69-77
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    • 2006
  • Background : Mesenchymal stem cells (MSCs) are present in most of the tissue matrix, taking part in their regeneration when injury or damage occurs. The aim of this study was to investigate the presence of cells with pluripotential characteristics in human subchondral bone and the capacity of these cells to differentiate to osteoblast. Methods : Human subchondral bone were digested with collagenase. Isolated cells were cultured with a-MEM, 15% FBS, 10-8M dexamethasone and 50 ng/mL ascoric acid. Cells from 0 day(isolated cells), 7 day (first subculture) and 14 days (third subculture) were used to carry out phenotypic characterization experiments flowcytometry analysis with 11 monoclonal antibodies) and osteogenic differentiation experiments. Osteogenic differentiation of cells was assessment by quantification of bone extracellular matrix components by following analysis: alkaline phosphatase(ALP) stains to detect ALP activity, RT-PCR and western blot to detect osteocalcin (OCN), osteopontin (OPN) and type I collagen(Col I), and Alizarin red stains to detect calcium deposition. Results : Flowcytometry analyses showed that in our population more than 98% of cells were positive for MSC markers: SH-2(CD105, 99%), CD29 (95%), CD73 (95%). Cells were negative for hematopoietic markers (CD11b, CD34, and CD45). Furthermore, cells showed positive stain to multipotent markers such as CDl17 (c-kit) (15.1%), and CD166 (74.9%), and cell adhesion molecules such as CD54 (78.1%) and CD106 (63.5%). The osteogenic specific marker analyses showed that the culture of these cells for 7 and 14 days stimulates ALP, OCN, OPN and Col I synthesis by RT-PCR and Western blot analysis. Also, after 14 days in the culture of MSCs induces mineralization by Arizarin red stain. Conclusion : In this work, we demonstrated a new and efficient method for osteoblastic differentiation of human subchondral bone stem cells. As MSCs takes part in reparative processes of adult tissues, these cells could play an important role in osteogenesis.

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골수유래줄기세포에서 분화된 골유사세포에서 ${\beta}-TCP$와 rhBMP-2의 골형성 효과에 관한 연구 (THE EFFECTS OF ${\beta}-TCP$/rhBMP-2 ON BONE FORMATION IN OSTEOBLAST-LIKE CELLS INDUCED FROM BONE MARROW-DERIVED MESENCHYMAL STEM CELLS)

  • 최용수;황경균;이재선;박창주;심광섭
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
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    • 제34권4호
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    • pp.419-427
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    • 2008
  • The present study aimed to investigate the osteogenic potentials of differentiated osteoblast-like cells (DOCs) induced from bone marrow-derived mesenchymal stem cells (MSCs) on ${\beta}-tricalcium$ phosphate (${\beta}-TCP$) with recombinant human bone morphogenetic protein (rhBMP-2) in vitro. Osteoblast differentiation was induced in confluent cultures by adding 100 nM dexamethasone, 10 mM ${\beta}$-glycerophosphate, 50 mM L-ascorbic acid. The Alizarin red S staining and reverse transcriptase-polymerase chain reaction (RT-PCR) were perfomed to examine the mRNA expression of alkaline phosphatase (ALP), bone sialoprotein (BSP), osteocalcin (OCN), receptor activator for nuclear factor ${\kappa}B$ ligand (RANKL), runt-related transcription factor 2 (RUNX2), collagen-Ⅰ (COL-Ⅰ). There were no significant differences in the osteogenic potentials of DOCs induced from MSCs on ${\beta}-TCP(+/-)$. According to the incubation period, there were significant increasing of Alizadin red S staining in the induction 3 weeks. The mRNA expression of ALP, RUNX2, and RANKL were higher in DOCs/${\beta}-TCP(-)$ than DOCs/${\beta}-TCP(+)$. According to rhBMP-2 concentrations, the mRNA expression of BSP was significantly increased in DOCs/${\beta}-TCP(+)$ compared to that of DOCs/${\beta}-TCP(-)$ on rhBMP 10 ng/ml. Our study presented the ${\beta}-TCP$ will have the possibility that calcium phosphate directly affect the osteoblastic differentiation of the bone marrowderived MSCs.

자기 활성 세포 분리법과 군체 분리법으로 분리된 건 줄기세포의 자가 재생 능력 및 분화능 효율 비교 (Comparison of Efficiency of Self-renewal and Differentiation Potential in Tendon-derived Mesenchymal Stem Cells Isolated by Magnetic-activated Cell Sorting Method or Colony Picking Method)

  • 이모세;최유림;윤동석;이진우;윤길성;최우진;한승환
    • 대한족부족관절학회지
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    • 제18권3호
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    • pp.100-107
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    • 2014
  • Purpose: The purpose of this study is to evaluate the efficacy of mesenchymal stem cell (MSC) isolation by the magnetic-activated cell sorting (MACS) method in tendon tissue-derived cells compared to the colony picking method for isolation of MSCs by picking colony-forming cells. Materials and Methods: Human tendon-derived cells were isolated by enzyme digestion using normal tendon tissues from three donors. We used the magnetic kit and well-known MSC markers (CD90 or CD105) to isolate MSCs in tendon-derived cells using MACS. Cloning cylinders were used to isolate colony-forming cells having MSC characteristics in tendon-derived cells. Colony-forming unit-fibroblast (CFU-F) assay was used to evaluate the self-renewal capacity of cells isolated using the colony picking method or MACS. For comparison of differentiation potentials into osteogenic or adipogenic lineage between two groups, alizarin red S and oil red O staining were performed at 14 days after induction of differentiation in vitro. Results: Flow cytometry results showed that early passage tendon-derived cells expressed CD44 in 99.13%, CD90 in 56.51%, and CD105 in 86.19%. In the CFU-F assay, CD90+ or CD105+ cells isolated with MACS showed larger colony formation in size than cells isolated using the colony picking method. We also observed that CD90+ or CD105+ cells were constantly differentiated into both osteogenic and adipogenic lineages in cells from all donors, whereas cells isolated using the colony picking method were heterogeneous in differentiation potentials to the osteogenic and adipogenic lineages. Conclusion: CD90+ or CD105+ cells isolated using MACS showed superior MSC characteristics in the self-renewal and multi-differentiation capacities compared with cells isolated using the colony picking method.

Comparison of Gene Expression Levels of Porcine Satellite Cells from Postnatal Muscle Tissue during Differentiation

  • Jeong, Jin Young;Kim, Jang Mi;Rajesh, Ramanna Valmiki;Suresh, Sekar;Jang, Gul Won;Lee, Kyung-Tai;Kim, Tae Hun;Park, Mina;Jeong, Hak Jae;Kim, Kyung Woon;Cho, Yong Min;Lee, Hyun-Jeong
    • Reproductive and Developmental Biology
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    • 제37권4호
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    • pp.219-224
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    • 2013
  • Muscular satellite cell (SC), which is stem cell of postnatal pig, is an important for study of differentiation into adipogenesis, myogenesis, and osteoblastogenesis. In this study, we isolated and examined from pig muscle tissue to determine capacity in proliferate, differentiate, and expression of various genes. Porcine satellite cells (PSC) were isolated from semimembranosus (SM) muscles of 90~100 days old pigs according to standard conditions. The cell proliferation increased in multi-potent cell by Masson's, oil red O, and Alizarin red staining respectively. We performed the expression levels of differentiation related genes using real-time PCR. We found that the differentiation into adipocyte increased expression levels of both fatty acid binding protein 4 (FABP4) and peroxisome proliferator-activated receptor gamma ($PPAR{\gamma}$) genes (p<0.01). Myocyte increased the expression levels of the myosin heavy chain (MHC), myogenic factor 5 (Myf5), myogenic regulatory factor (MyoD), and Myogenic factor 4 (myogenin) (p<0.01). Osteoblast increased the expression levels of alkaline phosphatase (ALP) (p<0.01). Finally, porcine satellite cells were induced to differentiate towards adipogenic, myogenic, and osteoblastogenic lineages. Our results suggest that muscle satellite cell in porcine may influence cell fate. Understanding the progression of PSC may lead to improved strategies for augmenting meat quality.