Developmental Glycobiology Section, NIDCR, National Institutes of Health, Bethesda, MD 20892-4370.
NIDCR Imaging Core, NIDCR, National Institutes of Health, Bethesda, MD 20892-4370.
Proc Natl Acad Sci U S A. 2022 Oct 25;119(43):e2209750119. doi: 10.1073/pnas.2209750119. Epub 2022 Oct 17.
Mucins are large, highly glycosylated transmembrane and secreted proteins that line and protect epithelial surfaces. However, the details of mucin biosynthesis and packaging in vivo are largely unknown. Here, we demonstrate that multiple distinct mucins undergo intragranular restructuring during secretory granule maturation in vivo, forming unique structures that are spatially segregated within the same granule. We further identify temporally-regulated genes that influence mucin restructuring, including those controlling pH (), Ca ions () and Cl ions ( and ). Finally, we show that altered mucin glycosylation influences the dimensions of these structures, thereby affecting secretory granule morphology. This study elucidates key steps and factors involved in intragranular, rather than intergranular segregation of mucins through regulated restructuring events during secretory granule maturation. Understanding how multiple distinct mucins are efficiently packaged into and secreted from secretory granules may provide insight into diseases resulting from defects in mucin secretion.
黏蛋白是一类富含糖基的跨膜和分泌型蛋白,排列于上皮细胞表面并起到保护作用。然而,黏蛋白在体内的生物合成和包装细节在很大程度上仍是未知的。在这里,我们证明了在体内分泌颗粒成熟过程中,多种不同的黏蛋白会发生颗粒内重排,形成独特的结构,这些结构在同一颗粒内被空间分隔开。我们进一步鉴定了影响黏蛋白重排的受时调控基因,包括控制 pH 值的基因 ()、钙离子 () 和氯离子 ()。最后,我们表明,黏蛋白糖基化的改变会影响这些结构的尺寸,从而影响分泌颗粒的形态。本研究阐明了在分泌颗粒成熟过程中通过有调控的重排事件发生的颗粒内而非颗粒间黏蛋白分隔的关键步骤和因素。了解多种不同的黏蛋白如何被有效地包装到分泌颗粒中并从其中分泌出来,可能有助于深入理解由于黏蛋白分泌缺陷而导致的疾病。