In treated cells, CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) is produced primarily in the endoplasmic reticulum (ER) and then transported to the plasma membrane. The CFTR protein undergoes post-translational modifications in the ER and Golgi apparatus before being folded correctly and sent to the cell surface, where it functions as a chloride channel. Proper trafficking and expression at the plasma membrane are crucial for its function in regulating ion transport.
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