Secretory ferritins mediate iron delivery during magnetite tooth formation in chitons

Iron is essential to most organisms, yet unbound iron is toxic, necessitating tight regulation of its storage and transport. Chitons concentrate extraordinary amounts of iron in radular tissue to form magnetite-mineralized teeth, but how iron is supplied to developing teeth remains unclear. Here, synchrotron radiation X-ray fluorescence mapping resolved the spatiotemporal redistribution of iron from the radular epithelium toward developing teeth. Integrated transcriptomic and proteomic analyses identified secretory ferritin subunits in radular tissue whose genes were highly expressed in the midgut gland and whose proteins were also present in the hemolymph. In vivo fluorescence tracking showed that circulating ferritin was selectively taken up by the radular epithelium, and following injection of Ag-loaded hemolymph ferritin, Ag was detected in developing teeth. Together, these findings support a model in which secretory ferritins produced in the midgut gland transport iron through the hemolymph to the radula, enabling the pronounced iron accumulation required for tooth mineralization.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-10-27
DOI
https://doi.org/10.64898/2026.10.23.761458
Primary Topic
Iron Metabolism and Disorders
Type
preprint

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preprint

Secretory ferritins mediate iron delivery during magnetite tooth formation in chitons

Masahiro Shimizu, Yuki Fujii, David Kisailus, Tsukasa Nakamura et al.
1 links
bioRxiv (Cold Spring Harbor Laboratory)
Iron Metabolism and Disorders
preprint

Secretory ferritins mediate iron delivery during magnetite tooth formation in chitons

Masahiro Shimizu, Yuki Fujii, David Kisailus, Tsukasa Nakamura, Kiori Obuse, Michiko Nemoto, Kenji Okoshi, Toshiya Senda, Shino Homma‐Takeda, Rui Onishi, Koki Okada, Akira Satoh, Nicole Angeline Robles Vizconde
preprint en

Abstract

Iron is essential to most organisms, yet unbound iron is toxic, necessitating tight regulation of its storage and transport. Chitons concentrate extraordinary amounts of iron in radular tissue to form magnetite-mineralized teeth, but how iron is supplied to developing teeth remains unclear. Here, synchrotron radiation X-ray fluorescence mapping resolved the spatiotemporal redistribution of iron from the radular epithelium toward developing teeth. Integrated transcriptomic and proteomic analyses identified secretory ferritin subunits in radular tissue whose genes were highly expressed in the midgut gland and whose proteins were also present in the hemolymph. In vivo fluorescence tracking showed that circulating ferritin was selectively taken up by the radular epithelium, and following injection of Ag-loaded hemolymph ferritin, Ag was detected in developing teeth. Together, these findings support a model in which secretory ferritins produced in the midgut gland transport iron through the hemolymph to the radula, enabling the pronounced iron accumulation required for tooth mineralization.

bioRxiv (Cold Spring Harbor Laboratory)
Toho University (JP), High Energy Accelerator Research Organization (JP), Okayama University (JP), University of California, Irvine (US), Kyoto University (JP), National Institutes for Quantum Science and Technology (JP)
Japan Agency for Medical Research and Development, Ministry of Education, Culture, Sports, Science and Technology, Japan Society for the Promotion of Science, Japan Science and Technology Agency, Institute of Genetics, Fusion Oriented REsearch for disruptive Science and Technology
Iron Metabolism and Disorders
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