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10.1172/jci.insight.203698
1Department of Pediatrics, Yale University School of Medicine, New Haven, United States of America
2Department of Obstetrics, Gynecology and Reproductive Sciences, Yale University School of Medicine, New Haven, United States of America
3Department of Immunobiology, Yale University School of Medicine, New Haven, United States of America
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Phan, L.
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1Department of Pediatrics, Yale University School of Medicine, New Haven, United States of America
2Department of Obstetrics, Gynecology and Reproductive Sciences, Yale University School of Medicine, New Haven, United States of America
3Department of Immunobiology, Yale University School of Medicine, New Haven, United States of America
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1Department of Pediatrics, Yale University School of Medicine, New Haven, United States of America
2Department of Obstetrics, Gynecology and Reproductive Sciences, Yale University School of Medicine, New Haven, United States of America
3Department of Immunobiology, Yale University School of Medicine, New Haven, United States of America
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1Department of Pediatrics, Yale University School of Medicine, New Haven, United States of America
2Department of Obstetrics, Gynecology and Reproductive Sciences, Yale University School of Medicine, New Haven, United States of America
3Department of Immunobiology, Yale University School of Medicine, New Haven, United States of America
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1Department of Pediatrics, Yale University School of Medicine, New Haven, United States of America
2Department of Obstetrics, Gynecology and Reproductive Sciences, Yale University School of Medicine, New Haven, United States of America
3Department of Immunobiology, Yale University School of Medicine, New Haven, United States of America
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1Department of Pediatrics, Yale University School of Medicine, New Haven, United States of America
2Department of Obstetrics, Gynecology and Reproductive Sciences, Yale University School of Medicine, New Haven, United States of America
3Department of Immunobiology, Yale University School of Medicine, New Haven, United States of America
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Kliman, H.
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1Department of Pediatrics, Yale University School of Medicine, New Haven, United States of America
2Department of Obstetrics, Gynecology and Reproductive Sciences, Yale University School of Medicine, New Haven, United States of America
3Department of Immunobiology, Yale University School of Medicine, New Haven, United States of America
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Konnikova, L.
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Published October 13, 2026 - More info
Although 95% of serotonin in the human body is produced in the gastrointestinal tract, most prior research work has focused on the brain. Despite its abundance in the gut, serotonin’s role in early intestinal development remains poorly understood. Here we show that serotonin is detected in both the small intestine and large intestine as early as 14 to 15 weeks gestational age. Using single-cell transcriptomics with histological validation, we generated a spatiotemporal atlas of serotonin and serotonin-related genes in the human gut from first trimester to late adulthood. The serotonin synthesis gene, TPH1, was exclusively expressed in enteroendocrine cells at all time points analyzed, with the highest expression in the second trimester. The serotonin reuptake gene, SLC6A4, was largely restricted to mature absorptive enterocytes and increased postnatally. Serotonin receptors also displayed distinct cellular and developmental expression patterns. HTR1E was confined to the first trimester during highly proliferative stage. HTR4 was enriched for in crypt regions, suggesting a role in proliferation for serotonin. Finally, HTR3E was associated with tuft cells throughout development. Together, these findings reveal the dynamic, cell-type-specific regulation of serotonin in the developing human gut, suggesting its importance in early intestinal development, and provide a framework to study its roles in intestinal development and diseases.