bioRxiv Science⌕ Search

bioRxiv · 10.64898/2026.10.16.759678

KRT7 Marks an Airway Glandular Ductal Stem Cell Population That Supports Multilineage Development and Regeneration

Abstract

Airway submucosal glands (SMGs) play a central role in host defense through mucus secretion, airway hydration, and mucociliary clearance. However, the hierarchical organization of glandular progenitor populations remains poorly defined, largely because SMGs are sparse and restricted to the proximal trachea in murine models. Using the ferret, a model that closely recapitulates the gland-rich submucosal architecture of human cartilaginous airways, we identify KRT7+ glandular ductal epithelial cells as a progenitor population. In both adult ferret and healthy human airways, KRT7 expression is primarily restricted to the SMG duct epithelium, where it is co-expressed with KRT19 and CD166 but only partially overlaps with ALDH1A1. During early postnatal development, KRT7 expression becomes progressively restricted to glandular ductal epithelium and is ultimately excluded from mature acinar, myoepithelial cells, and KRT5+/KRT14+ basal lineages. Fate mapping in KRT7CreER;ROSAmTmG transgenic ferrets revealed that KRT7-lineage cells serve as multipotent progenitors during SMG morphogenesis, generating both serous and mucous epithelial cells. Following severe airway injury, KRT7-lineage cells survive within gland ducts and rapidly expand to repair the damaged surface epithelium by differentiating into ciliated and secretory cells but not KRT5+ basal cells. In organoid cultures, glandular KRT7-lineage cells acquired a KRT5+ basal-like phenotype and generated multilineage epithelia with functional CFTR-mediated transport. These findings identify the KRT7+ ductal niche as a critical progenitor reservoir for airway development, homeostasis, and regeneration, with implications for cystic fibrosis therapies.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Hu, Z., Wang, C., Ma, Y., Yi, Y., Yang, L., Jiang, L., Yan, Z., Sun, X., Liu, X., Engelhardt, J. F.. 2026-10-19. KRT7 Marks an Airway Glandular Ductal Stem Cell Population That Supports Multilineage Development and Regeneration. https://doi.org/10.64898/2026.10.16.759678

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

The Structural Basis of Genome Silencing: The Inactive X Chromosome Resolved by Electron Spectroscopic Imaging

The eukaryotic nucleus has a hierarchical organization that permits genomic regulation. The genome is packaged as chromatin, which is silenced conditionally as facultative heterochromatin, or more stably silenced as constitutive heterochromatin. The smaller fractions of the genome that contain gene-rich sequences are organized into open chromatin conformations known as euchromatin. The inactive X (Xi) chromosome territory presents a uniquely powerful model system to investigate chromosome-scale gene silencing, as the entire chromosome undergoes coordinated epigenetic repression. The unique chromosome-wide silencing event provides a tractable system for investigating how molecular mechanisms of gene repression are translated into mesoscale structural features. This work builds on previous structural studies of the Xi that have leveraged conventional electron microscopy (EM) and cryo-EM, which have led to remarkable insights into the structural underpinnings of genome silencing. These approaches, however, are unable to directly distinguish chromatin from RNA and protein features. To resolve the molecular composition of the Xi chromosome territory and to provide a model of the structural organization of the chromatin, RNA and protein we analyzed the Xi using Electron Spectroscopic Imaging (ESI). We are able to resolve structural features without the use of contrast enhancing stains, using the distinct elemental signatures of chromatin, RNA and protein and combining them into composite images. By coupling ESI and electron tomography, we can circumvent the projection limitation of EM and provide an unprecedented view of the spatial organization of chromatin fibres in relation to structural features including RNA and proteins in 3D. Additionally, we employed correlative light-microscopy with ESI in physical serial sections and computationally assembled a structural model of the entire Xi chromosome territory revealing an intricate spatial network with distinct chromatin domains, distributed RNA-protein clusters, and identified a large, and previously uncharacterized mesoscale non-chromatin structure. Together, these observations provide new insights into the architecture of the Xi chromosome territory and shed electrons on the structural basis of chromosome-scale genome organization.

cell biology↗

STRIPAK associates with Rabex5-Rabaptin5 to promote Rab5-dependent early endosome formation and EGFR transport

His Domain Protein Tyrosine Phosphatase (HD-PTP) is required for multivesicular body (MVB) formation and endosome maturation, with Rab5-GTP levels raised upon HD-PTP depletion (Parkinson et al., 2021. doi: 10/1242/jcs.259192). Mass Spectrometry-based interactomics revealed that HD-PTP depletion increased association of Rabaptin5, a component of the early endosome Rabex5-Rabaptin5 Rab5-GEF, with multiple components of STRIPAK (striatin-interacting phosphatase and kinase). Native IPs and co-expression studies confirmed association between STRIPAK and Rabex5-Rabaptin5, including Strip1-Rabex5 and SLMAP-Rabaptin5 interactions. Consistent with functional Rabaptin5-STRIPAK links, co-depletion of Strip1 or Rabaptin5 with HD-PTP restored normal early endosome positioning and Rab5 distribution. Strip1 depletion impaired formation of central, Rab5-positive early endosomes, reduced cellular Rab5-GTP levels, and prevented the accumulation of internalised EGF-EGFR into centrally located endosomes. SLMAP depletion accentuated the central clustering of early endosomes and other endosomal compartments while also retarding the generation of new, EGFR-containing endosomes and EGFR lysosomal transport. We conclude that STRIPAK is a novel co-assembly factor of Rabex5-Rabaptin5, exerting subunit-specific effects on early endosomes.

cell biology↗

Simvastatin Preserves Human Microvascular Endothelial Barrier Function Through Mevalonate-Dependent Regulation of RhoB Localization and Activation

Endothelial barrier failure contributes to edema, tissue hypoperfusion, and organ dysfunction during inflammatory critical illness. RhoB has emerged as a regulator of tight junction disruption in human microvascular endothelial cells, but whether clinically used drugs can modulate RhoB-dependent barrier failure remains unclear. We tested whether simvastatin preserves human dermal microvascular endothelial cell barrier function during TNF stimulation and examined the role of mevalonate-dependent RhoB localization and activation. Simvastatin pretreatment attenuated TNF-induced loss of transendothelial electrical resistance and preserved junctional ZO-1 and claudin-5 organization. Simvastatin reduced membrane-associated and increased nuclear RhoB, decreased active RhoB, and suppressed myosin light chain phosphorylation. RhoB silencing phenocopied the barrier-protective effect of simvastatin, and combined RhoB silencing and simvastatin did not provide additive protection. Mevalonate supplementation reversed simvastatin-mediated preservation of barrier function, restored peripheral RhoB localization, and restored MLC phosphorylation. These findings identify mevalonate-dependent RhoB spatial regulation as a statin-sensitive mechanism contributing to inflammatory microvascular barrier dysfunction.

cell biology↗