den Hollander Lianne, Han HongMei, de Winter Matthijs, Svensson Lennart, Masich Sergej, Daneholt Bertil, Norlén Lars
Department of Cell and Molelcular Biology, Karolinska Institutet, 17177 Stockholm, Sweden.
Acta Derm Venereol. 2016 Mar;96(3):303-8. doi: 10.2340/00015555-2249.
Improved knowledge of the topology of lamellar bodies is a prerequisite for a molecular-level understanding of skin barrier formation, which in turn may provide clues as to the underlying causes of barrier-deficient skin disease. The aim of this study was to examine the key question of continuity vs. discreteness of the lamellar body system using 3 highly specialized and complementary 3-dimensional (3D) electron microscopy methodologies; tomography of vitreous sections (TOVIS), freeze-substitution serial section electron tomography (FS-SET), and focused ion beam scanning electron microscopy (FIB-SEM) tomography. We present here direct evidence that lamellar bodies are not discrete vesicles, but are part of a tubuloreticular membrane network filling out the cytoplasm and being continuous with the plasma membrane of stratum granulosum cells. This implies that skin barrier formation could be regarded as a membrane folding/unfolding process, but not as a lamellar body fusion process.
深入了解板层小体的拓扑结构是从分子水平理解皮肤屏障形成的前提条件,而这反过来又可能为屏障缺陷性皮肤病的潜在病因提供线索。本研究的目的是使用3种高度专业化且互补的三维(3D)电子显微镜方法,即玻璃切片断层扫描(TOVIS)、冷冻置换连续切片电子断层扫描(FS-SET)和聚焦离子束扫描电子显微镜(FIB-SEM)断层扫描,来研究板层小体系统的连续性与离散性这一关键问题。我们在此提供直接证据表明,板层小体不是离散的囊泡,而是构成管状网状膜网络的一部分,该网络填充细胞质并与颗粒层细胞的质膜相连。这意味着皮肤屏障形成可被视为一个膜折叠/展开过程,而非板层小体融合过程。