Multiple plasma membrane reporters discern LHFPL5 region that blocks trafficking to the plasma membrane

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作者
David C. Soler
Angela Ballesteros
Andrew E. Sloan
Thomas S. McCormick
Ruben Stepanyan
机构
[1] University Hospitals Cleveland Medical Center,Department of Neurosurgery
[2] University Hospitals Cleveland Medical Center,Brain Tumor and Neuro
[3] Case Western Reserve University School of Medicine,Oncology Center
[4] National Institutes of Health,University Hospitals
[5] Case Western Reserve University,Cleveland Medical Center and the Case Comprehensive Cancer Center
[6] University Hospitals Case Medical Center,National Institute on Deafness and Other Communication Disorders
[7] Case Western Reserve University,Department of Dermatology
[8] Case Western Reserve University,Murdough Family Center for Psoriasis
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摘要
The mechano-electrical transduction (MET) channel of the inner ear receptor cells, termed hair cells, is a protein complex that enables our senses of hearing and balance. Hair cell MET requires an elaborate interplay of multiple proteins that form the MET channel. One of the MET complex components is the transmembrane protein LHFPL5, which is required for hair cell MET and hearing. LHFPL5 is thought to form a multi-protein complex with other MET channel proteins, such as PCDH15, TMIE, and TMC1. Despite localizing to the plasma membrane of stereocilia, the mechanosensing organelles of hair cells, LHFPL5 requires its binding partner within the MET complex, PCDH15, to localize to the stereocilia tips in hair cells and to the plasma membrane in heterologous cells. Using the Aquaporin 3-tGFP reporter (AGR) for plasma membrane localization, we found that a region within extracellular loop 1, which interacts with PCDH15, precludes the trafficking of AGR reporter to the plasma membrane in heterologous cell lines. Our results suggest that the presence of protein partners may mask endoplasmic reticulum retention regions or enable the proper folding and trafficking of the MET complex components, to facilitate expression of the MET complex at the stereocilia membrane.
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