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Updated: Feb 27, 2026

Quantitating Iron Transport Across the Mouse Placenta In Vivo Using Nonradioactive Iron Isotopes
Published on: May 10, 2022
The transferrin receptor: the cellular iron gate.
Elena Gammella1, Paolo Buratti, Gaetano Cairo
1Department of Biomedical Sciences for Health, University of Milan, Via Mangiagalli 31, 20133 Milano, Italy. gaetano.cairo@unimi.it.
The transferrin receptor (TfR1) controls cellular iron uptake, a vital process for preventing iron overload. This review details the latest molecular regulation of TfR1 expression and its functions beyond iron delivery.
Area of Science:
- Molecular Biology
- Cell Biology
- Physiology
Background:
- The transferrin receptor (TfR1) is crucial for cellular iron uptake via clathrin-dependent endocytosis.
- TfR1 expression levels dictate the rate of cellular iron entry, impacting iron homeostasis.
- Precise control of TfR1 expression is essential to prevent cellular iron overload.
Purpose of the Study:
- To review recent advancements in the molecular regulation of transferrin receptor 1 (TfR1) expression.
- To explore the multifaceted functions of TfR1 beyond its established role in iron supply.
- To provide a comprehensive overview of TfR1's significance in cellular iron metabolism.
Main Methods:
- Literature review of recent studies on TfR1 molecular regulation.
- Analysis of current research on TfR1 function and expression control.
- Synthesis of data on TfR1's role in cellular iron homeostasis.
Main Results:
- TfR1 expression is regulated at multiple molecular levels.
- Recent advances have elucidated novel mechanisms controlling TfR1 transcription, translation, and protein stability.
- Emerging evidence highlights TfR1's involvement in cellular processes independent of iron transport.
Conclusions:
- Understanding TfR1 regulation is key to managing iron homeostasis and related disorders.
- TfR1 possesses diverse functions critical for various cell types and physiological conditions.
- Further research into TfR1's non-canonical roles may reveal new therapeutic targets.
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