华西医科大学学报
華西醫科大學學報
화서의과대학학보
JOURNAL OF WEST CHINA UNIVERSITY OF MEDICAL SCIENCES
2001年
1期
1-4
,共4页
杨志明%余希杰%黄富国%解慧琪
楊誌明%餘希傑%黃富國%解慧琪
양지명%여희걸%황부국%해혜기
成骨细胞%细胞外基质%Ⅰ型胶原%组织工程
成骨細胞%細胞外基質%Ⅰ型膠原%組織工程
성골세포%세포외기질%Ⅰ형효원%조직공정
目的 研究Ⅰ型胶原对人胚骨膜来源成骨细胞生物学特性的影响,为Ⅰ型胶原在组织工程人工骨中的应用提供依据。方法 [HTSS在不同浓度Ⅰ型胶原涂层上培养成骨细胞,用细胞计数法研究成骨细胞粘附情况,3H-TdR掺入实验观察成骨细胞增殖能力,通过检测成骨细胞胶原、骨钙素和碱性磷酸酶的合成情况,以不涂层Ⅰ型胶原为对照组,比较骨膜来源成骨细胞成骨能力的改变。结果 Ⅰ型胶原对成骨细胞发挥以下作用:①增加粘附细胞数量,且在25μg/ml浓度达最大效应;②减弱成骨细胞增殖能力,且以12.5μg/ml以上浓度作用显著(P<0.05);③轻度减弱成骨细胞Ⅰ型胶原合成能力,以25μg/ml以上浓度作用显著(P<0.05);④增加骨钙素合成,以6.25μg/ml以上浓度作用显著(P<0.05),25μg/ml浓度达最大效应;⑤增加成骨细胞碱性磷酸酶活性,以12.5μg/ml以上浓度作用显著(P<0.05)。结论 Ⅰ型胶原能促进成骨细胞的粘附与分化;支架材料上复合Ⅰ型胶原涂层可增强成骨细胞的成骨能力;Ⅰ型胶原最佳复合浓度为25μg/ml。
目的 研究Ⅰ型膠原對人胚骨膜來源成骨細胞生物學特性的影響,為Ⅰ型膠原在組織工程人工骨中的應用提供依據。方法 [HTSS在不同濃度Ⅰ型膠原塗層上培養成骨細胞,用細胞計數法研究成骨細胞粘附情況,3H-TdR摻入實驗觀察成骨細胞增殖能力,通過檢測成骨細胞膠原、骨鈣素和堿性燐痠酶的閤成情況,以不塗層Ⅰ型膠原為對照組,比較骨膜來源成骨細胞成骨能力的改變。結果 Ⅰ型膠原對成骨細胞髮揮以下作用:①增加粘附細胞數量,且在25μg/ml濃度達最大效應;②減弱成骨細胞增殖能力,且以12.5μg/ml以上濃度作用顯著(P<0.05);③輕度減弱成骨細胞Ⅰ型膠原閤成能力,以25μg/ml以上濃度作用顯著(P<0.05);④增加骨鈣素閤成,以6.25μg/ml以上濃度作用顯著(P<0.05),25μg/ml濃度達最大效應;⑤增加成骨細胞堿性燐痠酶活性,以12.5μg/ml以上濃度作用顯著(P<0.05)。結論 Ⅰ型膠原能促進成骨細胞的粘附與分化;支架材料上複閤Ⅰ型膠原塗層可增彊成骨細胞的成骨能力;Ⅰ型膠原最佳複閤濃度為25μg/ml。
목적 연구Ⅰ형효원대인배골막래원성골세포생물학특성적영향,위Ⅰ형효원재조직공정인공골중적응용제공의거。방법 [HTSS재불동농도Ⅰ형효원도층상배양성골세포,용세포계수법연구성골세포점부정황,3H-TdR참입실험관찰성골세포증식능력,통과검측성골세포효원、골개소화감성린산매적합성정황,이불도층Ⅰ형효원위대조조,비교골막래원성골세포성골능력적개변。결과 Ⅰ형효원대성골세포발휘이하작용:①증가점부세포수량,차재25μg/ml농도체최대효응;②감약성골세포증식능력,차이12.5μg/ml이상농도작용현저(P<0.05);③경도감약성골세포Ⅰ형효원합성능력,이25μg/ml이상농도작용현저(P<0.05);④증가골개소합성,이6.25μg/ml이상농도작용현저(P<0.05),25μg/ml농도체최대효응;⑤증가성골세포감성린산매활성,이12.5μg/ml이상농도작용현저(P<0.05)。결론 Ⅰ형효원능촉진성골세포적점부여분화;지가재료상복합Ⅰ형효원도층가증강성골세포적성골능력;Ⅰ형효원최가복합농도위25μg/ml。
Objective To study the influence of type Ⅰ coll agen(COL Ⅰ) onthe cell behavior of human periosteous osteoblasts(OB) and the application of type Ⅰ collagen in constructing bioactive artifical bone.Methods OB were cultured on dishes coated with bovine type Ⅰ collage n in different final concentrations. The cell adhesion was examined by the meth o ds of cell count, the proliferation of OB was studied by 3H-TdR, and the ost eoblastic ability was assessed by the synthesis of collagen, osteocalcin and alk aline phosphatase (ALP). Results OB cultured on type Ⅰ collage n layer had the following characteristicis: ① The amounts of adhesive cells we re maximal top in 25 μg/ml final concentration; ② The proliferation of OB was decreased above 12.5 μg/ml final concentration (P<0.05); ③ The synthesis of type Ⅰ collagen was reduced slightly (above 25 μg/ml,P<0.05); ④ The secretion of osteocalcin was increased markedly (above 6.25 μg/ml,P<0.05, w hich reached maximally in 25μg/ml); ⑤ The ALP activity was also increased (ab ove 12.5μg/ml, P<0.05). Conclusion Type Ⅰ collagen promot es the expression of osteoblastic phenotype and cell adhesion. When the scaffold materials for bone tissue engineering are coated with type Ⅰ collagen, the ost eogenesis of OB is enhanced to accelerate the tranformation course from artifici al bone to biological bone, the best final concentration is 25μg/ml.