CAJ | 학술논문

背景：干细胞培养基，尤其是乳腺干细胞培养基现阶段尚无有效的制备方法。目的：利用Sca-1+乳腺细胞验证自制乳腺干细胞培养基的有效性。<br>　　方法：用BM培养基培养乳腺器官样小体，6 d后以免疫荧光方法监测成纤维细胞Sca-1和vimentin的表达。筛选出MaECM培养基，培养乳腺细胞6 d后，免疫磁珠筛选Sca-1+和Sca-1-细胞群，流式细胞术分析Sca-1阳性细胞的纯度，1×104 Sca-1+或Sca-1-细胞种植在4只鼠双侧乳腺脂肪垫上，6-8周后取出乳腺脂肪垫，以卡红整体染色和苏木精-伊红染色分析长出乳腺的结构数量。<br>　　结果与结论：乳腺器官样小体用BM培养基培养6 d后，检测到大量Sca-1和vimentin阳性的成纤维细胞，说明BM培养基不适合分离Sca-1+乳腺干细胞。筛选出的MaECM培养基能够抑制成纤维的生长。磁珠筛选后，流式细胞术检测Sca-1+细胞在Sca-1+和Sca-1-细胞群的纯度分别是92%和5%。移植实验显示在8个种植Sca-1+细胞的脂肪垫生长出6个乳腺结构；而在8个种植Sca-1-细胞的脂肪垫中除1只鼠死亡，其余脂肪垫中均未长出乳腺结构。提示MaECM培养基适用于培养鼠乳腺干细胞。
배경：간세포배양기，우기시유선간세포배양기현계단상무유효적제비방법。목적：이용Sca-1+유선세포험증자제유선간세포배양기적유효성。<br>　　방법：용BM배양기배양유선기관양소체，6 d후이면역형광방법감측성섬유세포Sca-1화vimentin적표체。사선출MaECM배양기，배양유선세포6 d후，면역자주사선Sca-1+화Sca-1-세포군，류식세포술분석Sca-1양성세포적순도，1×104 Sca-1+혹Sca-1-세포충식재4지서쌍측유선지방점상，6-8주후취출유선지방점，이잡홍정체염색화소목정-이홍염색분석장출유선적결구수량。<br>　　결과여결론：유선기관양소체용BM배양기배양6 d후，검측도대량Sca-1화vimentin양성적성섬유세포，설명BM배양기불괄합분리Sca-1+유선간세포。사선출적MaECM배양기능구억제성섬유적생장。자주사선후，류식세포술검측Sca-1+세포재Sca-1+화Sca-1-세포군적순도분별시92%화5%。이식실험현시재8개충식Sca-1+세포적지방점생장출6개유선결구；이재8개충식Sca-1-세포적지방점중제1지서사망，기여지방점중균미장출유선결구。제시MaECM배양기괄용우배양서유선간세포。
BACKGROUND:Now in mammary stem cellresearch, no proper mammary stem cellmedium is provided to culture mammary stem cells. OBJECTIVE:To create a mammary stem cellmedium and validate its application by isolating Sca-1+mammary stem cells. METHODS:We first used BM medium to culture mammary organoids, and after 6 days, the expression of Sca-1 and vimentin was detected in fibroblasts by immunofluoresence method. Then, we established MaECM medium which arrested fibroblasts growth. After 6 days culture of mammary organoids by MaECM medium, Sca-1+and Sca-1-cellpopulations were sorted out by magnetic sorting and the purity was analyzed by flow cytometry. Sorted 1×104 Sca-1+or Sca-1-cells were transplanted into the bilateral mammary fat pads of four mice, and after 6-8 weeks, the fat pads were harvested for whole-mount immunohistochemical analysis and hematoxylin-eosin staining. RESULTS AND CONCLUSION:After 6 days culture of mammary organoids under BM medium, smal-sized colonies were generated around lots of fibroblasts. Immunofluoresence staining detected strong expression of vimentin and Sca-1 in fibroblasts, indicating that the BM medium is not suitable to isolate Sca-1+mammary stem cell. The MaECM medium promoted the proliferation of mammary epithelial cells whereas arrested fibroblasts growth. After 6 days culture of mammary organoids under MaECM medium and magnetic sorting, the flow cytometry showed that the purity of Sca-1+cellreached 92%and 5%in the Sca-1+and Sca-1-population, respectively. The results from transplantation test showed that six mammary outgrowths were regenerated out of eight injected fat pads in the Sca-1+cells transplantation, but in the Sca-1-transplantation population, one mouse died and the other transplants failed to produce outgrowths. We developed the MaECM medium which promoted the proliferation of mammary epithelial cells whereas arrested Sca-1+fibroblasts growth. Using the medium, we confirmed that Sca-1+mammary cells have capacity of isolating mammary stem cells.