Lumican

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Ideogram human chromosome 12

Lumican

Lumican is a protein that in humans is encoded by the LUM gene. It is a member of the small leucine-rich proteoglycan (SLRP) family. Lumican is a key component of the extracellular matrix in various tissues, including the cornea, skin, and heart.

Structure[edit | edit source]

Lumican consists of a core protein with attached glycosaminoglycan chains. It contains leucine-rich repeats that are involved in protein-protein interactions and binding to other extracellular matrix components.

Function[edit | edit source]

Lumican plays a crucial role in regulating collagen fibril assembly and organization. It interacts with collagen fibers, contributing to the structural integrity and mechanical properties of tissues. Additionally, lumican has been implicated in cell adhesion, migration, and proliferation processes.

Clinical Significance[edit | edit source]

Mutations in the LUM gene can lead to various connective tissue disorders, affecting the integrity of tissues where lumican is abundant. Deficiencies in lumican have been associated with corneal dystrophies and skin abnormalities.

Role in the Cornea[edit | edit source]

In the cornea, lumican is essential for maintaining transparency and proper refractive properties. It interacts with collagen fibrils to ensure the cornea's structural stability and optical clarity.

Role in the Skin[edit | edit source]

In the skin, lumican contributes to the organization of collagen fibers, influencing the skin's elasticity and strength. Alterations in lumican levels can impact skin aging and wound healing processes.

Role in the Heart[edit | edit source]

Lumican is also present in the heart, where it modulates the extracellular matrix composition and cardiac function. Changes in lumican expression have been linked to cardiac fibrosis and remodeling.

References[edit | edit source]

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Contributors: Prab R. Tumpati, MD