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Updated: Jun 18, 2025

A Murine Model of Fetal Exposure to Maternal Inflammation to Study the Effects of Acute Chorioamnionitis on Newborn Intestinal Development
Published on: June 24, 2020
CD71 + erythroid cells promote intestinal symbiotic microbial communities in pregnancy and neonatal period
Petya Koleva1, Jia He1, Garett Dunsmore1
1School of Dentistry, Division of Foundational Sciences, Faculty of Medicine and Dentistry, Edmonton, Canada.
Insights
CD71+ erythroid cells (CECs) are crucial for maintaining immune homeostasis in newborns. Their depletion disrupts the gut microbiome and immune responses, with lasting effects and sex-dependent differences, impacting human infant health.
Area of Science:
- Immunology
- Microbiology
- Neonatal Health
Background:
- Neonatal microbial community establishment is vital for immune development.
- CD71+ erythroid cells (CECs) influence immune responses to microbes.
- Previous work linked CEC depletion to inflammatory responses in newborn mice.
Purpose of the Study:
- To investigate the role of CECs in neonatal immune homeostasis and microbiome modulation.
- To determine the impact of CEC depletion on the developing immune system and gut microbiota.
- To explore potential implications for human neonatal health.
Main Methods:
- Systemic testing of CEC depletion using anti-CD71 antibody in neonatal mice.
- Analysis of immune markers including antimicrobial peptides (AMPs) and toll-like receptors (TLRs).
- Assessment of microbial community composition and diversity.
- Studies in pregnant mice and analysis of cord blood from preterm human newborns.
Main Results:
- Neonatal small intestinal lamina propria shows high CEC frequency due to erythropoiesis.
- CEC removal disrupts immune homeostasis, altering AMPs, TLRs, and cytokines, leading to microbial dysbiosis.
- Microbial alterations persist for at least 5 weeks post-treatment, with sex-dependent effects.
- CEC modulation impacts microbial communities in pregnant mice.
- Preterm newborns exhibit lower CEC proportions in cord blood.
Conclusions:
- CECs play a critical role in neonatal immune homeostasis and microbiome adaptation.
- CECs are key mediators in the host-microbiota dialogue within the neonatal gut.
- Findings suggest CECs have significant implications for human neonatal health and immune development.
Background:
The establishment of microbial communities in neonatal mammals plays a pivotal role in shaping their immune responses to infections and other immune-related conditions. This process is influenced by a combination of endogenous and exogenous factors. Previously, we reported that depletion of CD71 + erythroid cells (CECs) results in an inflammatory response to microbial communities in newborn mice.
Results:
Here, we systemically tested this hypothesis and observed that the small intestinal lamina propria of neonatal mice had the highest frequency of CECs during the early days of life. This high abundance of CECs was attributed to erythropoiesis niches within the small intestinal tissues. Notably, the removal of CECs from the intestinal tissues by the anti-CD71 antibody disrupted immune homeostasis. This disruption was evident by alteration in the expression of antimicrobial peptides (AMPs), toll-like receptors (TLRs), inflammatory cytokines/chemokines, and resulting in microbial dysbiosis. Intriguingly, these alterations in microbial communities persisted when tested 5 weeks post-treatment, with a more notable effect observed in female mice. This illustrates a sex-dependent association between CECs and neonatal microbiome modulation. Moreover, we extended our studies on pregnant mice, observing that modulating CECs substantially alters the frequency and diversity of their microbial communities. Finally, we found a significantly lower proportion of CECs in the cord blood of pre-term human newborns, suggesting a potential role in dysregulated immune responses to microbial communities in the gut.
Conclusions:
Our findings provide novel insights into pivotal role of CECs in immune homeostasis and swift adaptation of microbial communities in newborns. Despite the complexity of the cellular biology of the gut, our findings shed light on the previously unappreciated role of CECs in the dialogue between the microbiota and immune system. These findings have significant implications for human health. Video Abstract.
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