Iron-dependent apoptosis causes embryotoxicity in inflamed and obese pregnancy
Language English Country England, Great Britain Media electronic
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
Grant support
R01 HD096863
NICHD NIH HHS - United States
K01 DK127004
NIDDK NIH HHS - United States
T32 GM065823
NIGMS NIH HHS - United States
UL1 TR000124
NCATS NIH HHS - United States
F31 HD097931
NICHD NIH HHS - United States
UL1 TR001881
NCATS NIH HHS - United States
PubMed
34188052
PubMed Central
PMC8242011
DOI
10.1038/s41467-021-24333-z
PII: 10.1038/s41467-021-24333-z
Knihovny.cz E-resources
- MeSH
- Apoptosis physiology MeSH
- Embryo, Mammalian pathology MeSH
- Human Umbilical Vein Endothelial Cells MeSH
- Ferritins analysis MeSH
- Hepcidins genetics MeSH
- Pregnancy Complications MeSH
- Cells, Cultured MeSH
- Humans MeSH
- Mice, Inbred C57BL MeSH
- Mice, Knockout MeSH
- Mice MeSH
- Obesity pathology MeSH
- Placenta pathology MeSH
- Pregnancy MeSH
- Tumor Necrosis Factor-alpha metabolism MeSH
- Iron metabolism toxicity MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Mice MeSH
- Pregnancy MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
- Names of Substances
- Ferritins MeSH
- Hepcidins MeSH
- Tumor Necrosis Factor-alpha MeSH
- Iron MeSH
Iron is essential for a healthy pregnancy, and iron supplementation is nearly universally recommended, regardless of maternal iron status. A signal of potential harm is the U-shaped association between maternal ferritin, a marker of iron stores, and risk of adverse pregnancy outcomes. However, ferritin is also induced by inflammation and may overestimate iron stores during inflammation or infection. In this study, we use mouse models to determine whether maternal iron loading, inflammation, or their interaction cause poor pregnancy outcomes. Only maternal exposure to both iron excess and inflammation, but not either condition alone, causes embryo malformations and demise. Maternal iron excess potentiates embryo injury during both LPS-induced acute inflammation and obesity-induced chronic mild inflammation. The adverse interaction depends on TNFα signaling, causes apoptosis of placental and embryo endothelium, and is prevented by anti-TNFα or antioxidant treatment. Our findings raise important questions about the safety of indiscriminate iron supplementation during pregnancy.
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Fisher AL, Nemeth E. Iron homeostasis during pregnancy. Am. J. Clin. Nutr. 2017;106:1567S–1574S. doi: 10.3945/ajcn.117.155812. PubMed DOI PMC
Sangkhae V, et al. Effects of maternal iron status on placental and fetal iron homeostasis. J. Clin. Invest. 2020;130:625–640. doi: 10.1172/JCI127341. PubMed DOI PMC
Breymann C. Iron deficiency anemia in pregnancy. Semin. Hematol. 2015;52:339–347. doi: 10.1053/j.seminhematol.2015.07.003. PubMed DOI
Le CHH. The prevalence of anemia and moderate-severe anemia in the US population (NHANES 2003-2012) PLoS ONE. 2016;11:e0166635. doi: 10.1371/journal.pone.0166635. PubMed DOI PMC
WHO. Iron Deficiency Anaemia: Assesment, Prevention and Control: a Guide for Programme Managers. (World Health Organization, 2001).
Breuer W, et al. The assessment of serum nontransferrin-bound iron in chelation therapy and iron supplementation. Blood. 2000;95:2975–2982. doi: 10.1182/blood.V95.9.2975.009k03_2975_2982. PubMed DOI
Emerit J, Beaumont C, Trivin F. Iron metabolism, free radicals, and oxidative injury. Biomed. Pharmacother. 2001;55:333–339. doi: 10.1016/S0753-3322(01)00068-3. PubMed DOI
Tuck SM, Jensen CE, Wonke B, Yardumian A. Pregnancy management and outcomes in women with thalassaemia major. J. Pediatr. Endocrinol. Metab. 1998;11:923–928. PubMed
Fozza C, et al. Pregnancy outcome among women with beta-thalassemia major in North Sardinia. Acta Haematol. 2017;138:166–167. doi: 10.1159/000480450. PubMed DOI
Baron J, Ben-David G, Hallak M. Changes in non-transferrin-bound iron (NTBI) in pregnant women on iron supplements. Eur. J. Obstet. Gynecol. Reprod. Biol. 2008;140:281–282. doi: 10.1016/j.ejogrb.2008.01.002. PubMed DOI
Rawal S, et al. A longitudinal study of iron status during pregnancy and the risk of gestational diabetes: findings from a prospective, multiracial cohort. Diabetologia. 2017;60:249–257. doi: 10.1007/s00125-016-4149-3. PubMed DOI PMC
Scholl TO. Iron status during pregnancy: setting the stage for mother and infant. Am. J. Clin. Nutr. 2005;81:1218S–1222S. doi: 10.1093/ajcn/81.5.1218. PubMed DOI
Scholl TO, Reilly T. Anemia, iron and pregnancy outcome. J. Nutr. 2000;130:443S–447S. doi: 10.1093/jn/130.2.443S. PubMed DOI
Khambalia AZ, et al. High maternal iron status, dietary iron intake and iron supplement use in pregnancy and risk of gestational diabetes mellitus: a prospective study and systematic review. Diabet. Med. 2016;33:1211–1221. doi: 10.1111/dme.13056. PubMed DOI
Guo W, et al. Analysis of the correlation of gestational diabetes mellitus and peripheral ferritin with iron levels in early pregnancy. Minerva Endocrinol. 2019;44:91–96. PubMed
Lao TT, Chan PL, Tam KF. Gestational diabetes mellitus in the last trimester—a feature of maternal iron excess? Diabet. Med. 2001;18:218–223. doi: 10.1046/j.1464-5491.2001.00453.x. PubMed DOI
Hou J, Cliver SP, Tamura T, Johnston KE, Goldenberg R. Maternal serum ferritin and fetal growth. Obstet. Gynecol. 2000;95:447–452. PubMed
Gonzales GF, Steenland K, Tapia V. Maternal hemoglobin level and fetal outcome at low and high altitudes. Am. J. Physiol. Regulatory, Integr. Comp. Physiol. 2009;297:R1477–R1485. doi: 10.1152/ajpregu.00275.2009. PubMed DOI PMC
Knottnerus JA, Delgado LR, Knipschild PG, Essed GG, Smits F. Haematologic parameters and pregnancy outcome. A prospective cohort study in the third trimester. J. Clin. Epidemiol. 1990;43:461–466. doi: 10.1016/0895-4356(90)90134-B. PubMed DOI
Mamun AA, Padmadas SS, Khatun M. Maternal health during pregnancy and perinatal mortality in Bangladesh: evidence from a large-scale community-based clinical trial. Paediatr. Perinat. Epidemiol. 2006;20:482–490. doi: 10.1111/j.1365-3016.2006.00752.x. PubMed DOI
Scanlon KS, Yip R, Schieve LA, Cogswell ME. High and low hemoglobin levels during pregnancy: differential risks for preterm birth and small for gestational age. Obstet. Gynecol. 2000;96:741–748. PubMed
Stephansson O, Dickman PW, Johansson A, Cnattingius S. Maternal hemoglobin concentration during pregnancy and risk of stillbirth. JAMA. 2000;284:2611–2617. doi: 10.1001/jama.284.20.2611. PubMed DOI
Khambalia AZ, et al. High maternal serum ferritin in early pregnancy and risk of spontaneous preterm birth. Br. J. Nutr. 2015;114:455–461. doi: 10.1017/S0007114515001932. PubMed DOI
Xiao R, et al. Maternal second-trimester serum ferritin concentrations and subsequent risk of preterm delivery. Paediatr. Perinat. Epidemiol. 2002;16:297–304. doi: 10.1046/j.1365-3016.2002.00448.x. PubMed DOI
Lao TT, Tam K-F, Chan LY. Third trimester iron status and pregnancy outcome in non-anaemic women; pregnancy unfavourably affected by maternal iron excess. Hum. Reprod. 2000;15:1843–1848. doi: 10.1093/humrep/15.8.1843. PubMed DOI
Jones KL, et al. Autism with intellectual disability is associated with increased levels of maternal cytokines and chemokines during gestation. Mol. Psychiatry. 2017;22:273–279. doi: 10.1038/mp.2016.77. PubMed DOI PMC
Allswede, D. M., Yolken, R. H., Buka, S. L. & Cannon, T. D. Cytokine concentrations throughout pregnancy and risk for psychosis in adult offspring: a longitudinal case-control study. Lancet Psychiatry, 10.1016/S2215-0366(20)30006-7 (2020). PubMed PMC
Ginsberg Y, et al. Maternal infection requiring hospitalization during pregnancy and attention-deficit hyperactivity disorder in offspring: a quasi-experimental family-based study. J. Child Psychol. Psychiatry. 2019;60:160–168. doi: 10.1111/jcpp.12959. PubMed DOI
Atladottir HO, et al. Maternal infection requiring hospitalization during pregnancy and autism spectrum disorders. J. Autism Dev. Disord. 2010;40:1423–1430. doi: 10.1007/s10803-010-1006-y. PubMed DOI
Catalano PM, Shankar K. Obesity and pregnancy: mechanisms of short term and long term adverse consequences for mother and child. BMJ. 2017;356:j1. doi: 10.1136/bmj.j1. PubMed DOI PMC
Sanchez CE, et al. Maternal pre-pregnancy obesity and child neurodevelopmental outcomes: a meta-analysis. Obes. Rev. 2018;19:464–484. doi: 10.1111/obr.12643. PubMed DOI PMC
Choi GB, et al. The maternal interleukin-17a pathway in mice promotes autism-like phenotypes in offspring. Science. 2016;351:933–939. doi: 10.1126/science.aad0314. PubMed DOI PMC
Hsiao EY, Patterson PH. Activation of the maternal immune system induces endocrine changes in the placenta via IL-6. Brain Behav. Immun. 2011;25:604–615. doi: 10.1016/j.bbi.2010.12.017. PubMed DOI PMC
Wu W-L, Hsiao EY, Yan Z, Mazmanian SK, Patterson PH. The placental interleukin-6 signaling controls fetal brain development and behavior. Brain, Behav., Immun. 2017;62:11–23. doi: 10.1016/j.bbi.2016.11.007. PubMed DOI PMC
Garay PA, Hsiao EY, Patterson PH, McAllister AK. Maternal immune activation causes age- and region-specific changes in brain cytokines in offspring throughout development. Brain Behav. Immun. 2013;31:54–68. doi: 10.1016/j.bbi.2012.07.008. PubMed DOI PMC
Gücer F, et al. Maternal serum levels of tumor necrosis factor-α and interleukin-2 receptor in threatened abortion: a comparison with normal and pathologic pregnancies. Fertil. Steril. 2001;76:707–711. doi: 10.1016/S0015-0282(01)02002-7. PubMed DOI
Kaislasuo, J. et al. IL-10 to TNFalpha ratios throughout early first trimester can discriminate healthy pregnancies from pregnancy losses. Am. J. Reprod. Immunol. 83, e13195 (2019). PubMed PMC
Brown AS, et al. Elevated maternal interleukin-8 levels and risk of schizophrenia in adult offspring. Am. J. Psychiatry. 2004;161:889–895. doi: 10.1176/appi.ajp.161.5.889. PubMed DOI
Buka SL, et al. Maternal cytokine levels during pregnancy and adult psychosis. Brain Behav. Immun. 2001;15:411–420. doi: 10.1006/brbi.2001.0644. PubMed DOI
Canetta S, et al. Elevated maternal C-reactive protein and increased risk of schizophrenia in a national birth cohort. Am. J. Psychiatry. 2014;171:960–968. doi: 10.1176/appi.ajp.2014.13121579. PubMed DOI PMC
Racicot K, Mor G. Risks associated with viral infections during pregnancy. J. Clin. Investig. 2017;127:1591–1599. doi: 10.1172/JCI87490. PubMed DOI PMC
Adams Waldorf KM, McAdams RM. Influence of infection during pregnancy on fetal development. Reproduction. 2013;146:R151–R162. doi: 10.1530/REP-13-0232. PubMed DOI PMC
Ilievski V, Lu S-J, Hirsch E. Activation of toll-like receptors 2 or 3 and preterm delivery in the mouse. Reprod. Sci. 2007;14:315–320. doi: 10.1177/1933719107302959. PubMed DOI
Dudley DJ, Branch DW, Edwin SS, Mitchell MD. Induction of preterm birth in mice by RU486. Biol. Reprod. 1996;55:992–995. doi: 10.1095/biolreprod55.5.992. PubMed DOI
Elmore S. Apoptosis: a review of programmed cell death. Toxicol. Pathol. 2007;35:495–516. doi: 10.1080/01926230701320337. PubMed DOI PMC
Aronson D, et al. Obesity is the major determinant of elevated C-reactive protein in subjects with the metabolic syndrome. Int J. Obes. Relat. Metab. Disord. 2004;28:674–679. doi: 10.1038/sj.ijo.0802609. PubMed DOI
Katsuki A, et al. Serum levels of tumor necrosis factor-α are increased in obese patients with noninsulin-dependent diabetes mellitus1. J. Clin. Endocrinol. Metab. 1998;83:859–862. PubMed
Roytblat L, et al. Raised interleukin-6 levels in obese patients. Obes. Res. 2000;8:673–675. doi: 10.1038/oby.2000.86. PubMed DOI
WHO. WHO Recommendations on Antenatal Care for a Positive Pregnancy Experience. (World Health Organization, 2016). PubMed
Siu AL, U.S. Preventive Services Task Force Screening for iron deficiency anemia and iron supplementation in pregnant women to improve maternal health and birth outcomes: U.S. Preventive Services Task Force Recommendation Statement. Ann. Intern. Med. 2015;163:529–536. doi: 10.7326/M15-1707. PubMed DOI
Stoffel NU, von Siebenthal HK, Moretti D, Zimmermann MB. Oral iron supplementation in iron-deficient women: How much and how often? Mol. Asp. Med. 2020;75:100865. doi: 10.1016/j.mam.2020.100865. PubMed DOI
WHO. Daily iron and folic acid supplementation during pregnancy, http://www.who.int/elena/titles/daily_iron_pregnancy/en/ (2016).
USDA Agricultural Research Group Food Surveys Research Group. What We Eat in America, NHANES 2011-2012, Day 1 Food and Supplement Intake Data, https://www.ars.usda.gov/northeast-area/beltsville-md/beltsville-human-nutrition-research-center/food-surveys-research-group/ (2014).
Wang X, Garrick MD, Collins JF. Animal models of normal and disturbed iron and copper metabolism. J. Nutr. 2019;149:2085–2100. doi: 10.1093/jn/nxz172. PubMed DOI PMC
Domellof M. Benefits and harms of iron supplementation in iron-deficient and iron-sufficient children. Nestle Nutr. Workshop Ser. Pediatr. Program. 2010;65:153–162. discussion 162-155. doi: 10.1159/000281159. PubMed DOI
Uemura M, et al. Alpha-tocopherol prevents apoptosis of vascular endothelial cells via a mechanism exceeding that of mere antioxidation. Eur. J. Pharm. 2002;456:29–37. doi: 10.1016/S0014-2999(02)02639-0. PubMed DOI
Wu D, et al. Vitamin E reversed apoptosis of cardiomyocytes induced by exposure to high dose formaldehyde during mice pregnancy. Int Heart J. 2017;58:769–777. doi: 10.1536/ihj.16-279. PubMed DOI
Wu D, et al. Effects of vitamin E on reproductive protection in pregnant mice infected with pseudorabies virus (PRV) via regulating expression of Toll-like receptors (TLRs) and cytokine balance. J. Nutr. Sci. Vitaminol. (Tokyo) 2010;56:353–363. doi: 10.3177/jnsv.56.353. PubMed DOI
Li C-J, Li RW, Kahl S, Elsasser TH. Alpha-tocopherol alters transcription activities that modulates tumor necrosis factor alpha (TNF-α) Induced inflammatory response in bovine cells. Gene Regul. Syst. Bio. 2012;6:1–14. PubMed PMC
Devaraj S, Jialal I. Alpha-tocopherol decreases tumor necrosis factor-alpha mRNA and protein from activated human monocytes by inhibition of 5-lipoxygenase. Free Radic. Biol. Med. 2005;38:1212–1220. doi: 10.1016/j.freeradbiomed.2005.01.009. PubMed DOI
Huey KA, Fiscus G, Richwine AF, Johnson RW, Meador BM. In vivo vitamin E administration attenuates interleukin-6 and interleukin-1beta responses to an acute inflammatory insult in mouse skeletal and cardiac muscle. Exp. Physiol. 2008;93:1263–1272. doi: 10.1113/expphysiol.2008.043190. PubMed DOI PMC
Rumbold, A., Ota, E., Hori, H., Miyazaki, C. & Crowther, C. A. Vitamin E supplementation in pregnancy. Cochrane. Database. Syst. Rev.10.1002/14651858.CD004069.pub3 (2015). PubMed PMC
Aggarwal BB, Gupta SC, Kim JH. Historical perspectives on tumor necrosis factor and its superfamily: 25 years later, a golden journey. Blood. 2012;119:651–665. doi: 10.1182/blood-2011-04-325225. PubMed DOI PMC
Tzanavari T, Giannogonas P, Karalis KP. TNF-alpha and obesity. Curr. Dir. Autoimmun. 2010;11:145–156. doi: 10.1159/000289203. PubMed DOI
Berns M, Hommes DW. Anti-TNF-alpha therapies for the treatment of Crohn’s disease: the past, present and future. Expert Opin. Investig. Drugs. 2016;25:129–143. doi: 10.1517/13543784.2016.1126247. PubMed DOI
Dretzke J, et al. A systematic review and economic evaluation of the use of tumour necrosis factor-alpha (TNF-alpha) inhibitors, adalimumab and infliximab, for Crohn’s disease. Health Technol. Assess. 2011;15:1–244. doi: 10.3310/hta15060. PubMed DOI PMC
Mahadevan U, et al. Placental transfer of anti-tumor necrosis factor agents in pregnant patients with inflammatory bowel disease. Clin. Gastroenterol. Hepatol. 2013;11:286–292. doi: 10.1016/j.cgh.2012.11.011. PubMed DOI PMC
Kane SV, Acquah LA. Placental transport of immunoglobulins: a clinical review for gastroenterologists who prescribe therapeutic monoclonal antibodies to women during conception and pregnancy. Am. J. Gastroenterol. 2009;104:228–233. doi: 10.1038/ajg.2008.71. PubMed DOI
Julsgaard M, et al. Concentrations of adalimumab and infliximab in mothers and newborns, and effects on infection. Gastroenterology. 2016;151:110–119. doi: 10.1053/j.gastro.2016.04.002. PubMed DOI
Esteve-Solé, A. et al. Immunological changes in blood of newborns exposed to anti-TNF-α during Pregnancy. Front. Immunol.10.3389/fimmu.2017.01123 (2017). PubMed PMC
Mahadevan, U. et al. 1 Achievement of developmental milestones among offspring of women with inflammatory bowel disease: The PIANO Registry. Gastroenterology146, S–1 (2014).
Lesbordes-Brion JC, et al. Targeted disruption of the hepcidin 1 gene results in severe hemochromatosis. Blood. 2006;108:1402–1405. doi: 10.1182/blood-2006-02-003376. PubMed DOI
Fisher, A. L. et al. Fetal and amniotic fluid iron homeostasis in healthy and complicated murine, macaque, and human pregnancy. JCI Insight10.1172/jci.insight.135321 (2020). PubMed PMC
Edgar R, Domrachev M, Lash AE. Gene Expression Omnibus: NCBI gene expression and hybridization array data repository. Nucleic Acids Res. 2002;30:207–210. doi: 10.1093/nar/30.1.207. PubMed DOI PMC