RBP7
RBP7 or Retinol Binding Protein 7 is a protein that in humans is encoded by the RBP7 gene. It is a member of the lipocalin family and plays a significant role in the transport of retinol (vitamin A) from the liver storage site to peripheral tissues.
Function[edit | edit source]
RBP7 is a newly identified member of the retinol binding protein (RBP) family. It is known to be highly expressed in the epidermis and is believed to play a role in the cellular uptake and metabolism of retinol, which is crucial for skin homeostasis.
Structure[edit | edit source]
The RBP7 protein has a molecular weight of approximately 21 kDa and is composed of a single polypeptide chain. It shares a high degree of structural similarity with other members of the RBP family, including a hydrophobic pocket that is responsible for binding retinol.
Clinical Significance[edit | edit source]
While the exact role of RBP7 in human health and disease is still under investigation, it is believed to play a role in skin health due to its high expression in the epidermis and its involvement in retinol metabolism. Abnormalities in retinol metabolism have been linked to a variety of skin conditions, including psoriasis and acne.
Research[edit | edit source]
Current research is focused on further elucidating the role of RBP7 in retinol metabolism and skin health, as well as investigating potential therapeutic applications of modulating RBP7 activity.
See Also[edit | edit source]
References[edit | edit source]
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Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.Contributors: Prab R. Tumpati, MD