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Updated: Aug 13, 2026

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Published on: March 6, 2010
Langerin/CD207 sheds light on formation of birbeck granules and their possible function in Langerhans cells
Jenny Valladeau1, Colette Dezutter-Dambuyant, Sem Saeland
1INSERM U346, Hôpital Edouard Herriot, Lyon, France. valladeau@lyon.inserm.fr
Insights
Langerhans cells utilize Langerin (CD207) to form Birbeck granules, crucial for antigen capture and immune response initiation. This research deciphers Langerin's role in granule formation and function.
Area of Science:
- Immunology
- Cell Biology
- Dermatology
Background:
- Langerhans cells (LCs) are key immune sentinels in the epidermis and epithelia.
- LCs capture antigens and migrate to lymphoid tissues to initiate adaptive immunity.
- Birbeck granules (BGs) are unique structures within LCs, implicated in their function.
Purpose of the Study:
- To elucidate the role of Langerin (CD207) in the formation and function of Birbeck granules.
- To understand the molecular mechanisms underlying BG biogenesis.
Main Methods:
- Identification and characterization of Langerin/CD207.
- Transfection of Langerin cDNA into non-LCs (fibroblasts).
- Engineering of mutated and deleted Langerin forms to map functional domains.
Main Results:
- Langerin/CD207 is essential for Birbeck granule formation.
- Transfected Langerin induces BG-like membrane structures in fibroblasts.
- Specific domains of Langerin are critical for membrane zippering and superimposition.
Conclusions:
- Langerin acts as a specific regulator of membrane organization, driving BG formation.
- Langerin is a vital molecule for tracing LCs and investigating BG functions in immunity.
Abstract:
Langerhans cells (LCs) are immature dendritic cells of epidermis and epithelia, playing a sentinel role through their specialized function in antigen capture, and their capacity to migrate to secondary lymphoid tissue to initiate specific immunity. A unique feature of LCs is the presence of Birbeck granules (BGs), which are disks of two limiting membranes, separated by leaflets with periodic "zipperlike" striations. The recent identification of Langerin/CD207 has allowed researchers to decipher the mechanism of BG formation and approach an understanding of their function. Langerin is a type II lectin with mannose specificity expressed by LCs in epidermis and epithelia. Remarkably, transfection of Langerin cDNA into fibroblasts creates a dense network of membrane structures with features typical of BGs. Furthermore, mutated and deleted forms of Langerin have been engineered to map the functional domains essential for BG formation. Langerin is a potent LC-specific regulator of membrane superimposition and zippering, representing a key molecule to trace LCs and to probe BG function.
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