Hatzirodos Nicholas, Hummitzsch Katja, Irving-Rodgers Helen F, Rodgers Raymond J
Discipline of Obstetrics and Gynaecology, School of Paediatrics and Reproductive Health, Robinson Research Institute, University of Adelaide, Adelaide, South Australia, 5005, Australia.
School of Medical Science, Griffith University, Gold Coast, 4222, Queensland, Australia.
PLoS One. 2015 Mar 16;10(3):e0119800. doi: 10.1371/journal.pone.0119800. eCollection 2015.
In studies using isolated ovarian granulosa and thecal cells it is important to assess the degree of cross contamination. Marker genes commonly used for granulosa cells include FSHR, CYP19A1 and AMH while CYP17A1 and INSL3 are used for thecal cells. To increase the number of marker genes available we compared expression microarray data from isolated theca interna with that from granulosa cells of bovine small (n = 10 for both theca and granulosa cells; 3-5 mm) and large (n = 4 for both theca and granulosa cells, > 9 mm) antral follicles. Validation was conducted by qRT-PCR analyses. Known markers such as CYP19A1, FSHR and NR5A2 and another 11 genes (LOC404103, MGARP, GLDC, CHST8, CSN2, GPX3, SLC35G1, CA8, CLGN, FAM78A, SLC16A3) were common to the lists of the 50 most up regulated genes in granulosa cells from both follicle sizes. The expression in theca interna was more consistent than in granulosa cells between the two follicle sizes. Many genes up regulated in theca interna were common to both sizes of follicles (MGP, DCN, ASPN, ALDH1A1, COL1A2, FN1, COL3A1, OGN, APOD, COL5A2, IGF2, NID1, LHFP, ACTA2, DUSP12, ACTG2, SPARCL1, FILIP1L, EGFLAM, ADAMDEC1, HPGD, COL12A1, FBLN5, RAMP2, COL15A1, PLK2, COL6A3, LOXL1, RARRES1, FLI1, LAMA2). Many of these were stromal extracellular matrix genes. MGARP, GLDC, CHST8, GPX3 were identified as new potential markers for granulosa cells, while FBLN5, OGN, RAMP2 were significantly elevated in the theca interna.
在使用分离的卵巢颗粒细胞和卵泡膜细胞的研究中,评估交叉污染程度很重要。常用于颗粒细胞的标记基因包括促卵泡激素受体(FSHR)、细胞色素P450 19A1(CYP19A1)和抗缪勒管激素(AMH),而细胞色素P450 17A1(CYP17A1)和胰岛素样肽3(INSL3)用于卵泡膜细胞。为了增加可用标记基因的数量,我们比较了来自牛小(卵泡膜细胞和颗粒细胞均为n = 10;3 - 5毫米)和大(卵泡膜细胞和颗粒细胞均为n = 4,> 9毫米)窦状卵泡的分离的卵泡膜内层与颗粒细胞的表达微阵列数据。通过定量逆转录聚合酶链反应(qRT-PCR)分析进行验证。已知标记如CYP19A1、FSHR和核受体亚家族5,A组成员2(NR5A2)以及另外11个基因(LOC404103、MGARP、甘氨酸脱羧酶(GLDC)、糖胺聚糖硫酸转移酶8(CHST8)、β-酪蛋白(CSN2)、谷胱甘肽过氧化物酶3(GPX3)、溶质载体家族35,成员G1(SLC35G1)、碳酸酐酶8(CA8)、claudin(CLGN)、家族性肿瘤78A(FAM78A)、溶质载体家族16,成员3(SLC16A3))在两种卵泡大小的颗粒细胞中上调最多的50个基因列表中是共有的。卵泡膜内层的表达在两种卵泡大小之间比颗粒细胞更一致。许多在卵泡膜内层上调的基因在两种大小的卵泡中是共有的(基质Gla蛋白(MGP)、双调蛋白聚糖(DCN)、抑半胱氨酸蛋白酶蛋白(ASPN)、视黄醛脱氢酶1A1(ALDH1A1)、Ⅰ型胶原蛋白α2链(COL1A2)、纤连蛋白1(FN1)、Ⅲ型胶原蛋白α1链(COL3A1)、骨桥蛋白(OGN)、载脂蛋白D(APOD)、Ⅴ型胶原蛋白α2链(COL5A2)、胰岛素样生长因子2(IGF2)、巢蛋白1(NID1)、促黄体生成素结合蛋白(LHFP)、平滑肌肌动蛋白α2(ACTA2)、双特异性磷酸酶12(DUSP12)、肌动蛋白γ2(ACTG2)、富含半胱氨酸的分泌蛋白1(SPARCL1)、含Filamin样结构域蛋白1(FILIP1L)、表皮生长因子样黏附分子(EGFLAM)、含去整合素和金属蛋白酶结构域蛋白12(ADAMDEC1)、15-羟基前列腺素脱氢酶(HPGD)、Ⅻ型胶原蛋白α1链(COL12A1)、纤维连接蛋白5(FBLN5)、受体活性修饰蛋白2(RAMP2)、ⅩⅤ型胶原蛋白α1链(COL15A1)、丝氨酸/苏氨酸蛋白激酶2(PLK2)、Ⅵ型胶原蛋白α3链(COL6A3)、赖氨酰氧化酶样1(LOXL1)、视黄酸应答蛋白1(RARRES1)、Fli-1原癌基因(FLI1)、层粘连蛋白α2(LAMA2))。其中许多是基质细胞外基质基因。MGARP、GLDC、CHST8、GPX3被鉴定为颗粒细胞的新潜在标记,而FBLN5、OGN、RAMP2在卵泡膜内层中显著升高。