中华创伤骨科杂志
中華創傷骨科雜誌
중화창상골과잡지
CHINESE JOURNAL OF ORTHOPAEDIC TRAUMA
2010年
5期
463-466
,共4页
韩长旭%贾长青%刘振宁%梁峰%佟浩%柏树令
韓長旭%賈長青%劉振寧%樑峰%佟浩%柏樹令
한장욱%가장청%류진저%량봉%동호%백수령
成体干细胞%骨形态发生蛋白质类%转染%细胞分化
成體榦細胞%骨形態髮生蛋白質類%轉染%細胞分化
성체간세포%골형태발생단백질류%전염%세포분화
Adult stem cells%Bone morphogenetic proteins%Transfection%Cell differentiation
目的 探讨人骨形态发生蛋白-7(hBMP-7)基因修饰对兔脂肪干细胞(ADSCs)成骨能力的影响. 方法 原代培养兔脂肪干细胞,免疫组织化学方法检测细胞表面抗原CD44、CD49d、CD106的表达,对细胞进行鉴定;阳离子脂质体介导hBMP-7基因转染ADSCs,绿色荧光蛋白表达观察转染效率、逆转录-聚合酶链反应(RT-PCR)检测目的基因hBMP-7的表达;ALP定量测定,Western blot检测Ⅰ型胶原、骨钙素的表达,以评价转基因ADSCs向成骨细胞分化的情况. 结果 从兔脂肪组织中分离出来的ADSCs CD44、CD49d表达呈阳性,CD106表达呈阴性.RT-PCR检测筛选后的ADSCs稳定表达hBMP-7.转染后7、10、14 d ALP定量测定转染组明显高于未转染组,差异有统计学意义(P<0.05);成骨标志物Ⅰ型胶原、骨钙素的表达转染组明显高于未转染组.结论 从脂肪组织中分离出的ADSCs是一种较好的组织工程种子细胞.hBMP-7重组质粒转染ADSCs后表达目的蛋白,并诱导ADSCs向成骨细胞分化.
目的 探討人骨形態髮生蛋白-7(hBMP-7)基因脩飾對兔脂肪榦細胞(ADSCs)成骨能力的影響. 方法 原代培養兔脂肪榦細胞,免疫組織化學方法檢測細胞錶麵抗原CD44、CD49d、CD106的錶達,對細胞進行鑒定;暘離子脂質體介導hBMP-7基因轉染ADSCs,綠色熒光蛋白錶達觀察轉染效率、逆轉錄-聚閤酶鏈反應(RT-PCR)檢測目的基因hBMP-7的錶達;ALP定量測定,Western blot檢測Ⅰ型膠原、骨鈣素的錶達,以評價轉基因ADSCs嚮成骨細胞分化的情況. 結果 從兔脂肪組織中分離齣來的ADSCs CD44、CD49d錶達呈暘性,CD106錶達呈陰性.RT-PCR檢測篩選後的ADSCs穩定錶達hBMP-7.轉染後7、10、14 d ALP定量測定轉染組明顯高于未轉染組,差異有統計學意義(P<0.05);成骨標誌物Ⅰ型膠原、骨鈣素的錶達轉染組明顯高于未轉染組.結論 從脂肪組織中分離齣的ADSCs是一種較好的組織工程種子細胞.hBMP-7重組質粒轉染ADSCs後錶達目的蛋白,併誘導ADSCs嚮成骨細胞分化.
목적 탐토인골형태발생단백-7(hBMP-7)기인수식대토지방간세포(ADSCs)성골능력적영향. 방법 원대배양토지방간세포,면역조직화학방법검측세포표면항원CD44、CD49d、CD106적표체,대세포진행감정;양리자지질체개도hBMP-7기인전염ADSCs,록색형광단백표체관찰전염효솔、역전록-취합매련반응(RT-PCR)검측목적기인hBMP-7적표체;ALP정량측정,Western blot검측Ⅰ형효원、골개소적표체,이평개전기인ADSCs향성골세포분화적정황. 결과 종토지방조직중분리출래적ADSCs CD44、CD49d표체정양성,CD106표체정음성.RT-PCR검측사선후적ADSCs은정표체hBMP-7.전염후7、10、14 d ALP정량측정전염조명현고우미전염조,차이유통계학의의(P<0.05);성골표지물Ⅰ형효원、골개소적표체전염조명현고우미전염조.결론 종지방조직중분리출적ADSCs시일충교호적조직공정충자세포.hBMP-7중조질립전염ADSCs후표체목적단백,병유도ADSCs향성골세포분화.
Objective To explore the osteogenic potential of adipose-derived stem cells (ADSCs)when exposed to the cDNA of human bone morphogenetic protein-7 (hBMP-7) during osteoblast-differentiation in vitro. Methods The ADSCs were primarily cultured from rabbit fat tissue. CD44, CD49d and CD106 were detected and identified by immunohistochemistry. ADSCs were inducted with the method of stable transfection of pcDNA3. 1-GFP-hBMP-7 by Liprofectamine2000. The green fluorescent protein (GFP) expression was observed to access transfection efficiency of the transfected cells. RT-PCR was used to detect the expression of hBMP-7 gene in the induced ADSCs. The transform of ADSCs was assessed by detecting the ALP and expressions of collagen Ⅰ and osteocalcin. Results ADSCs were successfully isolated from rabbit adipose tissue. The isolated ADSCs expressed CD44 and CD49d but CD106 was absent. The pcDNA3. 1-GFP-hBMP-7 transfected ADSCs expressed hBMP-7. The intracellular ALP spectrophotometry in the hBMP-7 group was higher than in the control group after transfection. The expressions of collagen Ⅰ and osteocalcin in the hBMP-7 group were higher than in the control group. Conclusion ADSCs isolated from rabbit adipose tissue may be an excellent seeding cell for tissue engineering because they can differentiate into osteoblasts in vitro by hBMP-7 gene transfection.