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Flower dependent trafficking of lamellar bodies facilitates maturation of the epidermal barrier

Author

Listed:
  • Justin C. Rudd

    (Creighton University School of Medicine)

  • Jos P. H. Smits

    (Radboud Research Institute for Medical Innovation
    Heinrich Heine University)

  • Patrick T. Kuwong

    (Creighton University School of Medicine)

  • Rachel E. Johnson

    (Creighton University School of Medicine)

  • Louise M. N. Monga

    (Creighton University School of Medicine)

  • Ivonne M. J. J. Vlijmen-Willems

    (Radboud Research Institute for Medical Innovation)

  • Greer L. Porter

    (Creighton University School of Medicine)

  • Peter O. Halloran

    (Creighton University School of Medicine)

  • Kanika Sharma

    (University of Nebraska Medical Center)

  • Karina N. Schmidt

    (University of Washington)

  • Vikas Kumar

    (University of Nebraska Medical Center
    University of Nebraska Medical Center
    UMass Chan Medical School)

  • Justin G. Madson

    (Midwest Dermatology)

  • Mrinal K. Sarkar

    (University of Michigan)

  • Ellen H. Bogaard

    (Radboud Research Institute for Medical Innovation)

  • James A. Grunkemeyer

    (Creighton University School of Medicine)

  • Johann E. Gudjonsson

    (University of Michigan)

  • Sunny Y. Wong

    (University of Michigan
    University of Michigan)

  • Cory L. Simpson

    (University of Washington
    University of Washington)

  • Laura A. Hansen

    (Creighton University School of Medicine)

Abstract

Specialized secretory cells, including keratinocytes in the last viable layers of mammalian epidermis, utilize lysosome-related organelles (LROs) to exocytose distinct cargoes vital for tissue function. Here, we demonstrate that the Flower isoform, hFWE4, a putative Ca2+ channel that permits endocytic retrieval of presynaptic vesicles and lytic granules, also resides on epidermal lamellar bodies (LBs), an LRO that extrudes a proteinaceous lipid-rich matrix to finalize the epidermal barrier. In differentiated keratinocyte cultures, we show that hFWE4-positive LB-like vesicles associate with a distinct ensemble of LRO trafficking mediators and demonstrate that hFWE4 liberates Ca2+ from intracellular stores to enable the surface presentation of cargo contained within these vesicles. Finally, supporting a critical role for hFWE4-dependent trafficking in establishing the epidermal barrier, we demonstrate that this process is dysregulated in genetic diseases of cornification that are driven by impairments in keratinocyte Ca2+ handling. Our results provide new insight into the biogenesis and trafficking of epidermal LBs and more broadly suggest that hFWE4 may serve as a core component of LRO trafficking machinery that endows Ca2+ dependency to distinct stages of the transport process depending on the cell of origin.

Suggested Citation

  • Justin C. Rudd & Jos P. H. Smits & Patrick T. Kuwong & Rachel E. Johnson & Louise M. N. Monga & Ivonne M. J. J. Vlijmen-Willems & Greer L. Porter & Peter O. Halloran & Kanika Sharma & Karina N. Schmid, 2025. "Flower dependent trafficking of lamellar bodies facilitates maturation of the epidermal barrier," Nature Communications, Nature, vol. 16(1), pages 1-19, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-62105-1
    DOI: 10.1038/s41467-025-62105-1
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    References listed on IDEAS

    as
    1. Hankum Park & Frances V. Hundley & Qing Yu & Katherine A. Overmyer & Dain R. Brademan & Lia Serrano & Joao A. Paulo & Julia C. Paoli & Sharan Swarup & Joshua J. Coon & Steven P. Gygi & J. Wade Harper, 2022. "Spatial snapshots of amyloid precursor protein intramembrane processing via early endosome proteomics," Nature Communications, Nature, vol. 13(1), pages 1-21, December.
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    4. Xin Chen & Sarah M. Lloyd & Junghun Kweon & Giovanni M. Gamalong & Xiaomin Bao, 2021. "Epidermal progenitors suppress GRHL3-mediated differentiation through intronic polyadenylation promoted by CPSF-HNRNPA3 collaboration," Nature Communications, Nature, vol. 12(1), pages 1-15, December.
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