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作 者:凡孝菊[1,2] 陆伟[2] 余春艳[3] 徐军军[1,2] 李裕强[1] 金岩[2]
机构地区:[1]西北农林科技大学动物医学学院,陕西杨陵712100 [2]第四军医大学口腔医学院病理教研室,第四军医大学组织工程研发中心,陕西西安710032 [3]第四军医大学唐都医院,陕西西安710032
出 处:《中国皮肤性病学杂志》2008年第6期321-324,共4页The Chinese Journal of Dermatovenereology
基 金:国家高新技术发展规划(863计划)组织工程皮肤重大专项资助项目(2002AA205041)
摘 要:目的了解SD大鼠毛乳头细胞(DPCs)体外培养的生长特性,并用其构建组织工程双层皮肤。方法分离大鼠触须部获取完整毛囊,胶原酶消化获取毛乳头组织,组织块法培养毛乳头细胞并传代。以Ⅰ型胶原、α-平滑肌肌动蛋白(smooth muscle actin-α,SMA-α)、CK抗体免疫组化法鉴定细胞,MTT法检测并绘制细胞生长曲线。将第二代DPCs作为真皮种子细胞,角质形成细胞作为表皮种子细胞,用气-液面培养制备组织工程双层皮肤,HE染色观察其组织学结构。结果成功培养DPCs并传代,Ⅰ型胶原、SMA-α染色阳性;成功构建出含表皮与真皮层的组织工程双层皮肤。结论体外培养得到的DPCs与表皮结合较好,可作为组织工程皮肤的种子细胞。Objective To study the growth ability and characteristics in vitro of SD rat dermal papilla cells, and use them to construct tissue engineered skin. Methods The follicles were isolated from rat whiskers and were digested by collagenase to obtain dermal papillas, dermal papilla cells were cultured by the method of tissue culture and were passaged. The biological features of cultured cells were investigated by immunohistochemical method to detect the expression of α - smooth muscle actin, collagen I and CK, and the cell cycle was detected by MTT. The second passage DPCs were seeded in collagen and the keratinocytes were seeded on the surface to constructed tissue full - thickness engineered skin by the air - liquid interface method, stained by HE. Results DPCs were cultivated and passaged successfully, collagen I and SMA - α were expressed; The full - thickness tissue engineered skin was constructed successfully. Conclusion The DPCs cultivated in vitro were beneficial for connecting with epidermis, and DPCs could act as seed cells of tissue engineered skin.
分 类 号:R318[医药卫生—生物医学工程] R813.1[医药卫生—基础医学]
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