期刊
MOLECULAR GENETICS & GENOMIC MEDICINE
卷 9, 期 2, 页码 -出版社
WILEY
DOI: 10.1002/mgg3.1570
关键词
adiposity; choriodecidua; gene expression; human pregnancy; inflammation; leukocytes; maternal-fetal interface
资金
- Instituto Nacional de Perinatologia [21225002191]
- Consejo Nacional de Ciencia y Tecnologia [SALUD-2010-1-141144]
The study analyzed the relationship between maternal adiposity and inflammation-related gene expression in various types of leukocytes in six healthy pregnant women. The findings showed that increasing maternal adiposity correlated positively with genes related to activation, migration, infiltration, and proinflammation in maternal and placental leukocytes, but negatively with migration and infiltration genes in choriodecidual leukocytes. The results suggest that maternal adiposity may play a role in priming peripheral leukocytes and altering leukocyte recruitment and proinflammatory activity in pregnancy.
Background Human labor is associated with an inflammatory process that takes place at the maternal-fetal interface, where leukocytes infiltrate and contribute to the local production of effector molecules such as cytokines, chemokines, MMPs, etc. This process may be altered by a low-grade chronic inflammation, characteristic of obesity, resulting in adverse pregnancy outcomes. In this cross-sectional pilot study, we analyzed the relationship between maternal adiposity and inflammation-related gene expression in leukocytes from six healthy women with term pregnancies without labor. Methods We estimated maternal adiposity and examined the relative expression of 211 inflammation-related genes in maternal peripheral blood leukocytes (MAT), placental intervillous blood leukocytes (PLA), and choriodecidual leukocytes (CHD) by real-time qPCR. Finally, we analyzed the correlation between maternal adiposity and gene expression. Results Participants' adiposity ranged from 27.6% to 61.1% (n = 6). The expression of 23 genes significantly differed (p < 0.05) in MAT, PLA, and CHD leukocytes, most of which code for chemokines and proinflammatory cytokines. Importantly, increasing maternal adiposity correlated (r > 0.7) mostly positively with the expression of genes related to activation, migration, infiltration, and proinflammation in MAT (36 genes) and PLA (31 genes). In contrast, in CHD leukocytes maternal adiposity correlated only negatively with seven genes, involved in migration and infiltration. Conclusion Our findings suggest that during term pregnancy, increased maternal adiposity may enhance the priming of peripheral leukocytes, while in choriodecidua it may alter leukocyte recruitment and proinflammatory activity. Maternal adiposity must be considered an important variable in further studies that analyze inflammation-related gene expression in pregnant women.
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