中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2014年
21期
3329-3333
,共5页
赵刚%李京玲%王丹%于静%赵艳宇%满大鹏
趙剛%李京玲%王丹%于靜%趙豔宇%滿大鵬
조강%리경령%왕단%우정%조염우%만대붕
生物材料%纳米材料%NBD/RADA16%多肽水凝胶%三维培养%成骨细胞分化
生物材料%納米材料%NBD/RADA16%多肽水凝膠%三維培養%成骨細胞分化
생물재료%납미재료%NBD/RADA16%다태수응효%삼유배양%성골세포분화
hydrogel%peptides%osteoblasts
背景:RADA16是较成熟的自组装纳米短肽材料,在亲水面往复形成互补离子键,可组装为纳米纤维,并且能够促MC3T3 E1细胞的黏附、伸展和增殖。<br> 目的:观察新型自组装多肽水凝胶NBD/RADA16对小鼠前成骨细胞MC3T3 E1成骨分化能力的影响。<br> 方法:将MC3T3 E1细胞分别接种于自组装多肽水凝胶NBD/RADA16与RADA16水凝胶中,进行成骨诱导培养,以单纯成骨诱导培养的细胞为对照。诱导培养1,3,6 d检测细胞碱性磷酸酶活性;诱导培养7 d后, Western Blot检测细胞骨形态发生蛋白2的表达;诱导培养21 d后,茜素红染色观察细胞钙化结节。<br> 结果与结论:MC3T3 E1细胞在NBD/RADA16多肽水凝胶上生长状态良好,优于在RADA16上生长的细胞。自组装多肽水凝胶NBD/RADA16上MC3T3 E1细胞的碱性磷酸酶活性高于RADA16水凝胶上及单纯成骨诱导培养的细胞(P<0.01)。自组装多肽水凝胶NBD/RADA16上MC3T3 E1细胞的矿化基质沉积、骨形态发生蛋白2表达高于RADA16水凝胶上的细胞(P<0.01)。结果提示NBD/RADA16自组装多肽水凝胶较RADA16水凝胶更能促进MC3T3 E1细胞的成骨分化。
揹景:RADA16是較成熟的自組裝納米短肽材料,在親水麵往複形成互補離子鍵,可組裝為納米纖維,併且能夠促MC3T3 E1細胞的黏附、伸展和增殖。<br> 目的:觀察新型自組裝多肽水凝膠NBD/RADA16對小鼠前成骨細胞MC3T3 E1成骨分化能力的影響。<br> 方法:將MC3T3 E1細胞分彆接種于自組裝多肽水凝膠NBD/RADA16與RADA16水凝膠中,進行成骨誘導培養,以單純成骨誘導培養的細胞為對照。誘導培養1,3,6 d檢測細胞堿性燐痠酶活性;誘導培養7 d後, Western Blot檢測細胞骨形態髮生蛋白2的錶達;誘導培養21 d後,茜素紅染色觀察細胞鈣化結節。<br> 結果與結論:MC3T3 E1細胞在NBD/RADA16多肽水凝膠上生長狀態良好,優于在RADA16上生長的細胞。自組裝多肽水凝膠NBD/RADA16上MC3T3 E1細胞的堿性燐痠酶活性高于RADA16水凝膠上及單純成骨誘導培養的細胞(P<0.01)。自組裝多肽水凝膠NBD/RADA16上MC3T3 E1細胞的礦化基質沉積、骨形態髮生蛋白2錶達高于RADA16水凝膠上的細胞(P<0.01)。結果提示NBD/RADA16自組裝多肽水凝膠較RADA16水凝膠更能促進MC3T3 E1細胞的成骨分化。
배경:RADA16시교성숙적자조장납미단태재료,재친수면왕복형성호보리자건,가조장위납미섬유,병차능구촉MC3T3 E1세포적점부、신전화증식。<br> 목적:관찰신형자조장다태수응효NBD/RADA16대소서전성골세포MC3T3 E1성골분화능력적영향。<br> 방법:장MC3T3 E1세포분별접충우자조장다태수응효NBD/RADA16여RADA16수응효중,진행성골유도배양,이단순성골유도배양적세포위대조。유도배양1,3,6 d검측세포감성린산매활성;유도배양7 d후, Western Blot검측세포골형태발생단백2적표체;유도배양21 d후,천소홍염색관찰세포개화결절。<br> 결과여결론:MC3T3 E1세포재NBD/RADA16다태수응효상생장상태량호,우우재RADA16상생장적세포。자조장다태수응효NBD/RADA16상MC3T3 E1세포적감성린산매활성고우RADA16수응효상급단순성골유도배양적세포(P<0.01)。자조장다태수응효NBD/RADA16상MC3T3 E1세포적광화기질침적、골형태발생단백2표체고우RADA16수응효상적세포(P<0.01)。결과제시NBD/RADA16자조장다태수응효교RADA16수응효경능촉진MC3T3 E1세포적성골분화。
BACKGROUND:RADA16 is a mature amphiphilic self-assembling peptide, which can be assembled into nanofibers, and promote MC3T3 E1 cellattachment, spreading and proliferation. <br> OBJECTIVE:To observe the effects of the new-type self-assembling peptide hydrogel NBD/RADA16 on osteogenic differentiation of mouse preosteoblasts MC3T3 E1. <br> METHODS:The MC3T3 E1 cells were inoculated in NBD/RADA16 self-assembling peptide hydrogel and RADA16 hydrogel for osteogenic induction. cells undergoing simple osteogenic induction served as controls. After culture for 1, 3, 6 days, the activity of alkaline phosphatase was detected. After 7 days, western blot assay was used to determine the expression of bone morphogenetic protein-2. After 21 days, alizarin red staining was used to observe calcified nodules. <br> RESULTS AND CONCLUSION:MC3T3 E1 cells grew wel on the NBD/RADA16 peptide hydrogel, which were superior to those on the RADA16 hydrogel. The activity of alkaline phoshpatase was higher in the NBD/RADA16 group than the RADA16 and control groups (P<0.01). Compared with the RADA16 hydrogel, mineralized matrix deposition and expression of bone morphogenetic protein-2 were higher on the NBD/RADA16 peptide hydrogel (P<0.01). These findings indicate that the NBD/RADA16 peptide hydrogel is superior to the RADA16 hydrogel for promoting the osteogenic differentiation of MC3T3 E1 cells.