中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2013年
42期
7356-7362
,共7页
黄长智%杨效宁%刘大诚%孙一公%戴醒明
黃長智%楊效寧%劉大誠%孫一公%戴醒明
황장지%양효저%류대성%손일공%대성명
生物材料%组织工程骨材料%复合支架材料%降钙素基因相关肽%脂肪干细胞%成骨分化%藻酸钙凝胶%三维培养
生物材料%組織工程骨材料%複閤支架材料%降鈣素基因相關肽%脂肪榦細胞%成骨分化%藻痠鈣凝膠%三維培養
생물재료%조직공정골재료%복합지가재료%강개소기인상관태%지방간세포%성골분화%조산개응효%삼유배양
biocompatible materials%calcitonin gene-related peptide%gels%stem cells
背景:降钙素基因相关肽已被证实具有诱导成骨细胞分化作用,但其是否可使三维培养下的脂肪干细胞向成骨细胞分化构建组织工程骨的相关报道少见。<br> 目的:探讨外源性降钙素基因相关肽诱导兔脂肪干细胞复合藻酸钙凝胶三维培养成骨分化的可行性。<br> 方法:取新西兰兔双侧腹股沟区皮下脂肪垫,Ⅰ型胶原酶消化离心贴壁法分离培养脂肪干细胞,取第3代与海藻酸钠混合制备凝胶,于24孔板分组培养:对照组加入含10-2 mol/Lβ-甘油磷酸钠、10-7 mol/L地塞米松、50 mg/L抗坏血酸、体积分数10%胎牛血清的DMEM/F-12骨诱导培养基,实验组在此基础上再加入1.5μg/L降钙素基因相关肽进行诱导培养。于诱导不同时间点MTT法检测细胞增殖,RT-PCR法检测诱导细胞Ⅰ型胶原和骨钙素mRNA的表达,并检测碱性磷酸酶及钙离子浓度。<br> 结果与结论:兔脂肪干细胞的增殖曲线呈“S”型,实验组诱导1,3,5,7,14,21 d 的 A 值高于对照组(P<0.05);诱导2周后两组细胞碱性磷酸酶、茜素红染色均阳性,但实验组钙结节较对照组明显增多。实验组诱导7,14 d的Ⅰ型胶原和骨钙素mRNA表达均强于对照组。实验组诱导1,2,3,4周的碱性磷酸酶活性及钙离子浓度均高于对照组(P<0.05)。结果表明降钙素基因相关肽能诱导复合藻酸钙凝胶的脂肪干细胞向成骨细胞分化。
揹景:降鈣素基因相關肽已被證實具有誘導成骨細胞分化作用,但其是否可使三維培養下的脂肪榦細胞嚮成骨細胞分化構建組織工程骨的相關報道少見。<br> 目的:探討外源性降鈣素基因相關肽誘導兔脂肪榦細胞複閤藻痠鈣凝膠三維培養成骨分化的可行性。<br> 方法:取新西蘭兔雙側腹股溝區皮下脂肪墊,Ⅰ型膠原酶消化離心貼壁法分離培養脂肪榦細胞,取第3代與海藻痠鈉混閤製備凝膠,于24孔闆分組培養:對照組加入含10-2 mol/Lβ-甘油燐痠鈉、10-7 mol/L地塞米鬆、50 mg/L抗壞血痠、體積分數10%胎牛血清的DMEM/F-12骨誘導培養基,實驗組在此基礎上再加入1.5μg/L降鈣素基因相關肽進行誘導培養。于誘導不同時間點MTT法檢測細胞增殖,RT-PCR法檢測誘導細胞Ⅰ型膠原和骨鈣素mRNA的錶達,併檢測堿性燐痠酶及鈣離子濃度。<br> 結果與結論:兔脂肪榦細胞的增殖麯線呈“S”型,實驗組誘導1,3,5,7,14,21 d 的 A 值高于對照組(P<0.05);誘導2週後兩組細胞堿性燐痠酶、茜素紅染色均暘性,但實驗組鈣結節較對照組明顯增多。實驗組誘導7,14 d的Ⅰ型膠原和骨鈣素mRNA錶達均彊于對照組。實驗組誘導1,2,3,4週的堿性燐痠酶活性及鈣離子濃度均高于對照組(P<0.05)。結果錶明降鈣素基因相關肽能誘導複閤藻痠鈣凝膠的脂肪榦細胞嚮成骨細胞分化。
배경:강개소기인상관태이피증실구유유도성골세포분화작용,단기시부가사삼유배양하적지방간세포향성골세포분화구건조직공정골적상관보도소견。<br> 목적:탐토외원성강개소기인상관태유도토지방간세포복합조산개응효삼유배양성골분화적가행성。<br> 방법:취신서란토쌍측복고구구피하지방점,Ⅰ형효원매소화리심첩벽법분리배양지방간세포,취제3대여해조산납혼합제비응효,우24공판분조배양:대조조가입함10-2 mol/Lβ-감유린산납、10-7 mol/L지새미송、50 mg/L항배혈산、체적분수10%태우혈청적DMEM/F-12골유도배양기,실험조재차기출상재가입1.5μg/L강개소기인상관태진행유도배양。우유도불동시간점MTT법검측세포증식,RT-PCR법검측유도세포Ⅰ형효원화골개소mRNA적표체,병검측감성린산매급개리자농도。<br> 결과여결론:토지방간세포적증식곡선정“S”형,실험조유도1,3,5,7,14,21 d 적 A 치고우대조조(P<0.05);유도2주후량조세포감성린산매、천소홍염색균양성,단실험조개결절교대조조명현증다。실험조유도7,14 d적Ⅰ형효원화골개소mRNA표체균강우대조조。실험조유도1,2,3,4주적감성린산매활성급개리자농도균고우대조조(P<0.05)。결과표명강개소기인상관태능유도복합조산개응효적지방간세포향성골세포분화。
BACKGROUND:Calcitonin gene-related peptide has been confirmed to induce osteogenic differentiation, but whether it can induce the osteogenic differentiation of adipose-derived stem cells under three-dimensional culture to construct tissue-engineered bone is rarely reported. <br> OBJECTIVE:To investigate the feasibility of exogenous calcitonin gene-related peptide to induce osteogenic differentiation of adipose-derived stem cells combined with calcium alginate gel in three-dimensional condition. <br> METHODS:Adipose-derived stem cells were gained by col agenase I digestion of the subcutaneous adipose tissue of both inguinal regions of New Zealand rabbits. Passage 3 cells were mixed with sodium alginate to prepare calcium alginate gel, and then the cells were assigned into two groups and cultured in 24-wel plates. Adipose-derived stem cells in the control group were cultured in Dulbecco’s modified Eagle’s medium/Ham’s nutrient mixture F-12 supplemented with 10-2 mol/Lβ-glycerophosphate sodium, 10-7 mol/L dexamethasone, 50 mg/L ascorbic acid, 10%fetal bovine serum. While, adipose-derived stem cells in the experimental group were incubated with the same medium as above, but 1.5 μg/L calcitonin gene-related peptide was added. The cells proliferation and the mRNA expressions of col agen I and osteocalcin were detected by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide and reverse transcription-PCR respectively, and alkaline phosphatase and calcium concentration were detected at different induction time. <br> RESULTS AND CONCLUSION:The cellproliferation curves were S shaped. The absorbance values of the experimental group were higher than those of the control group at1, 3, 5, 7, 14, 21 days after osteogenic induction (P<0.05). Alkaline phosphatase and alizarin red staining of adipose-derived stem cells was al positive, but golden round nodes became more and bigger in the experimental group compared with the control group after 2 weeks. At 7 and 14 days, col agen I and osteocalcin mRNA expressions were higher in the experimental group than in the control group. Alkaline phosphatase activity and calcium concentration of the experimental group were higher than those of the control group at 1, 2, 3, 4 weeks after osteogenic induction (P<0.05). Results showed that the calcitonin gene-related peptide can induce the osteogenic differentiation of adipose-derived stem cells combined with calcium alginate gel.