Zhou Hong, Ohno Nobuhiko, Terada Nobuo, Saitoh Sei, Fujii Yasuhisa, Ohno Shinichi
Department of Anatomy, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, 1110 Shimokato, Chuo-City, Yamanashi 409-3898, Japan.
Reproduction. 2007 Aug;134(2):307-17. doi: 10.1530/REP-07-0062.
The molecular sieve with size- and charge selectivity in ovarian follicles, the so-called blood-follicle barrier (BFB), was examined during follicular development under physiological conditions to reveal ovarian structures responsible for the BFB by using our 'in vivo cryotechnique' (IVCT). Mouse ovary specimens were prepared with different methods including IVCT, immersion, or perfusion chemical fixation and quick-freezing following resection or perfusion. Their paraffin sections or cryosections were stained with hematoxylin-eosin or immunostained for serum proteins with different molecular weights: albumin, immunoglobulin (Ig) G1 heavy chain, inter-alpha-trypsin inhibitor (I alpha I), fibrinogen, and IgM. Their immunoreactivity was better preserved with IVCT. The immunostaining for albumin was clearly observed in blood vessels, interstitium, and developing follicles, but that of IgG1, I alpha I, or fibrinogen was significantly decreased inside the follicles. IgM was immunohistochemically decreased throughout the interstitium outside blood vessels. The immunoreactivities of IgG1 and IgM, as compared with albumin, were clearly changed along follicular basement membranes and around vascular endothelial cells respectively. These findings indicate that BFB functions throughout follicular development, and the follicular basement membrane and the vascular endothelium could play some significant roles in the permselectivity for such soluble proteins with intermediate and high molecular weight respectively.
利用我们的“体内冷冻技术”(IVCT),在生理条件下研究卵泡发育过程中具有大小和电荷选择性的分子筛,即所谓的血卵泡屏障(BFB),以揭示负责BFB的卵巢结构。采用包括IVCT、浸泡或灌注化学固定以及切除或灌注后快速冷冻等不同方法制备小鼠卵巢标本。对其石蜡切片或冷冻切片进行苏木精-伊红染色或用不同分子量的血清蛋白进行免疫染色:白蛋白、免疫球蛋白(Ig)G1重链、α-胰蛋白酶抑制剂(IαI)、纤维蛋白原和IgM。IVCT能更好地保存它们的免疫反应性。在血管、间质和发育中的卵泡中可清楚观察到白蛋白的免疫染色,但卵泡内IgG1、IαI或纤维蛋白原的免疫染色显著降低。IgM在血管外的整个间质中免疫组化降低。与白蛋白相比,IgG1和IgM的免疫反应性分别沿卵泡基底膜和血管内皮细胞周围明显改变。这些发现表明,BFB在卵泡发育过程中发挥作用,卵泡基底膜和血管内皮细胞可能分别在对中等和高分子量可溶性蛋白的通透选择性中发挥重要作用。