Fasciani Alessandro, Bocci Guido, Xu Jing, Bielecki Ryszard, Greenblatt Ellen, Leyland Nicholas, Casper Robert F
Department of Obstetrics and Gynecology, Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada.
Fertil Steril. 2003 Nov;80(5):1137-43. doi: 10.1016/s0015-0282(03)02164-2.
To reproduce the earliest phases of endometriosis using a new in vitro model in which cells from a cultured endometrial fragment can proliferate, invade, reconstitute new endometrial-like tissue, and generate blood vessels.
Experimental in vitro study.
A hospital-based academic research institute.
PATIENT(S): Five normal ovulating women undergoing surgery for various benign gynecological indications.
INTERVENTION(S): Endometrial samples obtained from the fundus of the uterine cavity were placed in a three-dimensional fibrin matrix culture system.
MAIN OUTCOME MEASURE(S): Degree of proliferation of stromal cells and invasion of the fibrin matrix, gland, and stroma formation, vessel sprouting, and immunohistochemical characterization of various cellular components.
RESULT(S): During the first week of culture, an endometrial cell outgrowth was observed from the original fragments in 120 of 144 wells (83.3%). Subsequently, cell outgrowths could be quantified in 132 (91.6%), 129 (89.5%), and 127 (88.1%) of the wells after 15, 60, and 90 days, respectively. An invasion of the matrix by the human endometrial cells led to the formation of tubular structures that coalesced into tissue, architecturally resembling endometrium and in which the glands were immunohistochemically positive for cytokeratin. New capillaries, immunohistochemically positive for CD31 and vimentin, sprouted from the endometrial outgrowths at the beginning of the fifth week of culture.
CONCLUSION(S): These data show that cells from endometrial explants can proliferate and invade a fibrin matrix in vitro generating new glands, stroma, and vessels consistent with endometriosis. The three-dimensional fibrin matrix used in the present study provides an opportunity to observe the earliest biological events of endometriosis in a quantifiable way.
使用一种新的体外模型重现子宫内膜异位症的最早阶段,在该模型中,来自培养的子宫内膜片段的细胞能够增殖、侵袭、重构新的子宫内膜样组织并生成血管。
体外实验研究。
一家医院的学术研究机构。
五名因各种良性妇科指征接受手术的正常排卵女性。
从子宫腔底部获取的子宫内膜样本被置于三维纤维蛋白基质培养系统中。
基质细胞的增殖程度、纤维蛋白基质的侵袭情况、腺体和基质形成、血管芽生以及各种细胞成分的免疫组织化学特征。
在培养的第一周,144个孔中有120个(83.3%)观察到来自原始片段的子宫内膜细胞生长。随后,分别在培养15天、60天和90天后,132个孔(91.6%)、129个孔(89.5%)和127个孔(88.1%)中的细胞生长情况可被量化。人子宫内膜细胞对基质的侵袭导致形成管状结构,这些结构融合成组织,在结构上类似于子宫内膜,其中腺体对细胞角蛋白免疫组织化学呈阳性。在培养第五周开始时,从子宫内膜生长物中长出了对CD31和波形蛋白免疫组织化学呈阳性的新毛细血管。
这些数据表明,子宫内膜外植体的细胞能够在体外增殖并侵袭纤维蛋白基质,生成与子宫内膜异位症一致的新腺体、基质和血管。本研究中使用的三维纤维蛋白基质提供了以可量化的方式观察子宫内膜异位症最早生物学事件的机会。