Liu Yanyan, Zhang Xuan, Zhang Lili, Zhu Hongmei, Chen Jiurong, Lin Ziyuan, Zhou Bin, Liu Shanling, Wang He, Sun Huaqin
Prenatal Diagnosis Center, Department of Obstetrics & Gynecologic, Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu 610041, People's Republic of China.
SCU-CUHK Joint Laboratory for Reproductive Medicine, Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, Department of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu 610041, People's Republic of China.
ACS Omega. 2022 Sep 28;7(40):35981-35992. doi: 10.1021/acsomega.2c05152. eCollection 2022 Oct 11.
Down syndrome (DS) is the most common chromosomal condition associated with intellectual disability and is characterized by a variety of additional clinical findings. The pathogenesis of DS and the differences between the sexes are not clear. In order to identify differentially expressed proteins that might be employed as potential biological markers and elucidate the difference in pathogenesis between different genders of T21 fetuses, providing clues for individualized detection and treatment is essential. Amniocyte samples of T21 males, T21 females, CN males, and CN females were collected by amniocentesis. The quantitative value of the peptide corresponding to each sample was determined through quantitative analysis by mass spectrometry. We identified many differentially expressed proteins between T21 fetuses and CN fetuses/T21 males and CN males/T21 females and CN females/and T21 males and T21 females. These differential proteins are associated with many important biological processes and affect the development of multiple systems, including the heart, hematopoietic, immune, reproductive, and nervous systems. Our results show sex-specific modulation of protein expression and biological processes and provide new insights into sex-specific differences in the pathogenesis of DS.
唐氏综合征(DS)是与智力残疾相关的最常见染色体疾病,其特征为伴有多种其他临床症状。DS的发病机制以及性别差异尚不清楚。为了鉴定可能用作潜在生物标志物的差异表达蛋白,并阐明T21胎儿不同性别之间发病机制的差异,为个体化检测和治疗提供线索至关重要。通过羊膜穿刺术收集T21男性、T21女性、染色体正常男性和染色体正常女性的羊水细胞样本。通过质谱定量分析确定每个样本对应肽段的定量值。我们鉴定出T21胎儿与染色体正常胎儿之间/T21男性与染色体正常男性之间/T21女性与染色体正常女性之间/以及T21男性与T21女性之间存在许多差异表达蛋白。这些差异蛋白与许多重要的生物学过程相关,并影响多个系统的发育,包括心脏、造血、免疫、生殖和神经系统。我们的结果显示了蛋白质表达和生物学过程的性别特异性调节,并为DS发病机制中的性别特异性差异提供了新的见解。