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
2期
183-186
,共4页
赵广%荆吉峰%张治宇%朱佳俊%崔岩
趙廣%荊吉峰%張治宇%硃佳俊%崔巖
조엄%형길봉%장치우%주가준%최암
组织构建%软骨组织构建%胰岛素样生长因子1%种子细胞%软骨细胞%创伤性关节炎%兔
組織構建%軟骨組織構建%胰島素樣生長因子1%種子細胞%軟骨細胞%創傷性關節炎%兔
조직구건%연골조직구건%이도소양생장인자1%충자세포%연골세포%창상성관절염%토
insulin-like growth factor I%arthritis%model,animals%chondrocytes%cell proliferation
背景:早期受损的软骨细胞在体外培养时容易产生去分化,表型不稳,常需添加一定的生长因子。<br> 目的:观察胰岛素样生长因子1对成年兔创伤性关节炎早期关节软骨细胞体外增殖的促进作用。<br> 方法:采用改良Hulth法制备成兔创伤性关节炎模型,造模成功后无菌条件下片状切取股骨远端及胫骨近端,用消化培养法培养软骨细胞。将软骨细胞随机分为2组,对照组加入含体积分数10%胎牛血清因子的DMEM培养液培养;实验组在对照组的基础上加入100μg/L的胰岛素样生长因子1。通过细胞形态学、细胞计数、细胞活性检测胰岛素样生长因子1对创伤性关节炎关节软骨细胞增殖的影响。<br> 结果与结论:成功培养出早期创伤性关节炎兔软骨细胞,细胞多数为小细胞,形态有小梭形、小圆形及小多边形。苏木精-伊红染色显示实验组细胞数量多于对照组,MTT 实验证实实验组细胞的吸光度值大于对照组(P<0.01)。结果提示,胰岛素样生长因子1能促进早期创伤性关节炎模型兔软骨细胞的体外增殖。
揹景:早期受損的軟骨細胞在體外培養時容易產生去分化,錶型不穩,常需添加一定的生長因子。<br> 目的:觀察胰島素樣生長因子1對成年兔創傷性關節炎早期關節軟骨細胞體外增殖的促進作用。<br> 方法:採用改良Hulth法製備成兔創傷性關節炎模型,造模成功後無菌條件下片狀切取股骨遠耑及脛骨近耑,用消化培養法培養軟骨細胞。將軟骨細胞隨機分為2組,對照組加入含體積分數10%胎牛血清因子的DMEM培養液培養;實驗組在對照組的基礎上加入100μg/L的胰島素樣生長因子1。通過細胞形態學、細胞計數、細胞活性檢測胰島素樣生長因子1對創傷性關節炎關節軟骨細胞增殖的影響。<br> 結果與結論:成功培養齣早期創傷性關節炎兔軟骨細胞,細胞多數為小細胞,形態有小梭形、小圓形及小多邊形。囌木精-伊紅染色顯示實驗組細胞數量多于對照組,MTT 實驗證實實驗組細胞的吸光度值大于對照組(P<0.01)。結果提示,胰島素樣生長因子1能促進早期創傷性關節炎模型兔軟骨細胞的體外增殖。
배경:조기수손적연골세포재체외배양시용역산생거분화,표형불은,상수첨가일정적생장인자。<br> 목적:관찰이도소양생장인자1대성년토창상성관절염조기관절연골세포체외증식적촉진작용。<br> 방법:채용개량Hulth법제비성토창상성관절염모형,조모성공후무균조건하편상절취고골원단급경골근단,용소화배양법배양연골세포。장연골세포수궤분위2조,대조조가입함체적분수10%태우혈청인자적DMEM배양액배양;실험조재대조조적기출상가입100μg/L적이도소양생장인자1。통과세포형태학、세포계수、세포활성검측이도소양생장인자1대창상성관절염관절연골세포증식적영향。<br> 결과여결론:성공배양출조기창상성관절염토연골세포,세포다수위소세포,형태유소사형、소원형급소다변형。소목정-이홍염색현시실험조세포수량다우대조조,MTT 실험증실실험조세포적흡광도치대우대조조(P<0.01)。결과제시,이도소양생장인자1능촉진조기창상성관절염모형토연골세포적체외증식。
BACKGROUND:The early damaged chondrocytes are susceptible to de-differentiate and exert unstable phenotype during the in vitro culture, thus needing some growth factors. <br> OBJECTIVE:To observe the promotion effect of insulin-like growth factor 1 on the in vitro proliferation of chondrocytes in adult rabbits with traumatic arthritis. <br> METHODS:Traumatic arthritis models of adult rabbits were established by using the modified Hulth method. After the models were successful y established, the distal femur and proximal tibia were harvested under sterile conditions, the chondrocytes were cultured. The cultured cells were divided into two groups:control group was cultured with Dulbecco’s modified Eagle’s medium containing 10%fetal bovine serum, while experimental group was cultured with Dulbecco's modified Eagle’s medium containing 100μg/L insulin-like growth factor 1. The effect of insulin-like growth factor 1 on the proliferation of chondrocytes in adult rabbits with traumatic arthritis was determined through the cytomorphology, cellcounting, and cellactivity. <br> RESULTS AND CONCLUSION:The chondrocytes in adult rabbits with traumatic arthritis were successful y cultured, the majority of cells were mini-cells, presenting smal fusiform, round or polygonal shape. Hematoxylin-eosin staining showed that the number of cells in experimental group was higher than that in control group. MTT assay found that the absorbance of cells in experimental group was greater than that in control group (P<0.01). Our findings indicate that, insulin-like growth factor 1 can promote the in vitro proliferation of chondrocytes in adult rabbits with traumatic arthritis.