Alam S M Khorshed, Konno Toshihiro, Soares Michael J
Department of Pathology and Laboratory MedicineInstitute for Reproductive Health and Regenerative Medicine, University of Kansas Medical Center, Kansas City, Kansas 66160, USA.
Department of Pathology and Laboratory MedicineInstitute for Reproductive Health and Regenerative Medicine, University of Kansas Medical Center, Kansas City, Kansas 66160, USA
Reproduction. 2015 Jun;149(6):625-32. doi: 10.1530/REP-15-0107.
Prolactin family 8, subfamily a, member 2 (PRL8A2; also called decidual prolactin-related protein; dPRP) is a member of the expanded prolactin family. PRL8A2 is expressed in the uterine decidua and contributes to pregnancy-dependent adaptations to hypoxia. The purpose of this study was to identify gene targets for PRL8A2 action within the uteroplacental compartment. Affymetrix DNA microarray analysis was performed for RNA samples from WT and Prl8a2 null tissues. Validation of the DNA microarray was performed using quantitative RT-PCR. Nine genes were confirmed with decreased expression in Prl8a2 null tissues (e.g., Klk7, Rimklb, Arhgef6, Calm4, Sprr2h, Prl4a1, Ccl27, Lipg, and Htra3). These include potential decidual, endothelial and trophoblast cell targets positively regulated by PRL8A2. A significant upregulation of Derl3, Herpud1, Creld2, Hsp90b1, Ddit3 and Hspa5 was identified in Prl8a2 null tissues, reflecting an increased endoplasmic reticulum (ER) stress response. ER stress genes were prominently expressed in the uterine decidua. We propose that PRL8A2 is a mediator of progesterone-dependent modulation of intrauterine responses to physiological stressors.
催乳素家族8,a亚家族,成员2(PRL8A2;也称为蜕膜催乳素相关蛋白;dPRP)是扩展的催乳素家族的成员。PRL8A2在子宫蜕膜中表达,并有助于孕期对缺氧的适应性变化。本研究的目的是确定PRL8A2在子宫胎盘区室作用的基因靶点。对野生型和Prl8a2基因敲除组织的RNA样本进行了Affymetrix DNA微阵列分析。使用定量RT-PCR对DNA微阵列进行验证。在Prl8a2基因敲除组织中,9个基因的表达被证实降低(例如,Klk7、Rimklb、Arhgef6、Calm4、Sprr2h、Prl4a1、Ccl27、Lipg和Htra3)。这些包括受PRL8A2正向调控的潜在蜕膜、内皮和滋养层细胞靶点。在Prl8a2基因敲除组织中,Derl3、Herpud1、Creld2、Hsp90b1、Ddit3和Hspa5显著上调,反映内质网(ER)应激反应增加。ER应激基因在子宫蜕膜中显著表达。我们提出PRL8A2是孕酮依赖性调节子宫对生理应激源反应的介质。