Betageri, Kalpana R.

Abstract Pulmonary fibrosis is increasingly understood to involve dysfunction within and across multiple cellular compartments, with recent attention highlighting the involvement of pulmonary vascular dysfunction in failed repair and progression of fibrosis. Formulation and delivery of lung-targeting lipid nanoparticles (LNPs) may provide a means to selectively target the lung but not systemic vasculature. However, the feasibility and efficacy of such approaches in the fibrotic lung are unknown. We sought to test whether intravenously administered lung-targeting LNPs can safely deliver mRNA to the healthy and fibrotic lung vasculature in young and aged mice and whether delivery of mRNA encoding a matricellular protein could promote fibrosis resolution. We used a selective organ targeting LNP formulation and characterized cell-specificity of delivery after bleomycin-induced lung fibrosis. We then delivered Ccn3 mRNA (encoding cellular communication network factor 3) to aged mice in the setting of established lung fibrosis and evaluated fibrotic regression and vascular repair. The matricellular protein encoded by Ccn3 was previously identified by our group as an important regulator of lung endothelial function. We found that LNP delivery was lung specific and predominantly endothelial targeting in the setting of lung fibrosis. Delivery of Ccn3 mRNA to aged mice via LNPs modestly reduced fibrosis and improved microvascular density in the lungs. Our results support the concept that cell-specific and repair-promoting cargos delivered via lung-targeting LNPs may have utility for treatment of established fibrosis.

Piezo2 is a mechanically gated ion channel most commonly expressed by specialized mechanoreceptors, such as the enteroendocrine cells (EECs) of the gastrointestinal epithelium. A subpopulation of EECs expresses Piezo2 and functionally resembles the skin’s touch sensors, called Merkel cells. Low-magnitude mechanical stimuli delivered to the mucosal layer are primarily sensed by mechanosensitive EECs in a process we term “gut touch.” Piezo2 transduces cellular forces into ionic currents, a process that is sensitive to bilayer tension and cytoskeletal depolymerization. E-cadherin is a widely expressed protein that mediates cell–cell adhesion in epithelia and interacts with scaffold proteins that anchor it to actin fibers. E-cadherin was shown to interact with Piezo2 in immortalized cell models. We hypothesized that the Piezo2–E-cadherin interaction is important for EEC mechanosensitivity. To test this, we used super-resolution imaging, co-immunoprecipitation, and functional assays in primary tissues from mice and gut organoids. In tissue EECs and intestinal organoids, we observed multiple Piezo2 cellular pools, including one that overlaps with actin and E-cadherin at the cells’ lateral walls. Further, E-cadherin co-immunoprecipitated with Piezo2 in the primary colonic epithelium. We found that E-cadherin knockdown decreases mechanosensitive calcium responses in mechanically stimulated primary EECs. In all, our results demonstrate that Piezo2 localizes to the lateral wall of EECs, where it physically interacts with E-cadherin and actin. They suggest that the Piezo2–E-cadherin–actin interaction is important for mechanosensitivity in the gut epithelium and possibly in tissues where E-cadherin and Piezo2 are co-expressed in epithelial mechanoreceptors, such as skin, lung, and bladder.

Aberrant vascular remodeling contributes to the progression of many aging-associated diseases, including idiopathic pulmonary fibrosis (IPF), where heterogeneous capillary density, endothelial transcriptional alterations, and increased vascular permeability correlate with poor disease outcomes. Thus, identifying disease-driving mechanisms in the pulmonary vasculature may be a promising strategy to limit IPF progression. Here, we identified Ccn3 as an endothelial-derived factor that is upregulated in resolving but not in persistent lung fibrosis in mice, and whose function is critical for vascular homeostasis and repair. Loss and gain of function experiments were carried out to test the role of CCN3 in lung microvascular endothelial function in vitro through RNAi and the addition of recombinant human CCN3 protein, respectively. Endothelial migration, permeability, proliferation, and in vitro angiogenesis were tested in cultured human lung microvascular endothelial cells (ECs). Loss of CCN3 in lung ECs resulted in transcriptional alterations along with impaired wound-healing responses, in vitro angiogenesis, barrier integrity as well as an increased profibrotic activity through paracrine signals, whereas the addition of recombinant CCN3 augmented endothelial function. Altogether, our results demonstrate that the matricellular protein CCN3 plays an important role in lung endothelial function and could serve as a promising therapeutic target to facilitate vascular repair and promote lung fibrosis resolution.

Enteric glia are important components of the enteric nervous system (ENS) that control critical functions of the alimentary canal including motility, fluid and ion transport, and immune barrier. Anatomical assessments of enteric glia to date have utilized microdissected whole‐mount tissue or thin sections to visualize cells in the optically dense matrix of the bowel. The aim of this study was to assess the morphological features of enteric glia throughout the small and large intestines of the mouse in intact full‐thickness preparations. B6.Cg‐Polr2atm1(CAG‐GCaMP5g,‐tdTomato)Tvrd/J mice were bred to homozygosity with B6.Cg‐Tg(SOX10‐cre/ERT2)Vpa mice which were maintained as hemizygous. Mice received a gavage of tamoxifen (5mg in 0.2ml corn oil) for five days at seven to eight weeks of age to induce tdTomato (tdT) expression in glia. Mice were euthanized by CO2 inhalation at 10–20 weeks of age. Jejunum and mid colon segments were opened on the mesenteric border, fixed in 4% paraformaldehyde, immunostained for anti‐S100β, and cleared with Ce3D solution. Tissues were imaged using confocal microscopy and 3D reconstructions were made using Analyze. SOX10‐tdT cells were found in the bowel throughout all layers. In the muscularis externa of both the jejunum and colon, there were extensive networks within myenteric ganglia, intraganglionic fiber tracts, within the circular muscle layer, along fiber tracts ascending through the circular muscle, and rare cells were observed in the longitudinal muscle layer. In the submucosal layer of both the jejunum and colon, SOX‐tdT cells were in submucosal ganglia, along intraganglionic fibers and formed a regular network of processes that extended within the lamina propria surrounding the base of intestinal crypts. In the mucosa, SOX10‐tdT distribution differed between the jejunum and colon. In the colonic mucosa, there were two distinct bands of SOX10‐tdT networks oriented perpendicular to and surrounding all colonic glands which were approximately 120μm in height. These bands were located approximately 20μm and 60μm from the base of the glands. SOX10‐tdT cells were very rarely observed near the luminal surface of the colonic glands. In the jejunal mucosa, there were extensive SOX10‐tdT networks throughout the lamina propria surrounding crypts and extending to the tips of villi. Overlap of SOX10‐tdT and S100β immunoreactivity was nearly 100% throughout all glial populations with two exceptions, only 10–20% of SOX10‐tdT cells had S100β immunoreactivity in the jejunum mucosa and there were submucosal neurons that expressed S100β that did not contain SOX10‐tdT. Collectively, these data demonstrate significant complexity of the glial networks of the intestines with distinct morphological differences between mucosal glia of the colon and jejunum that may implicate different functions of enteric glia in the small and large intestines. Support or Funding Information Supported by NIH grants R01DK106011, P30DK084567 and DP2AT010875 and Department of Defense grant W81XWH‐18‐1‐0218. Representative SOX10‐tdT fluorescence in projections of 409 or 139 1.22μm‐thick confocal images through the full thickness of either jejunum (left) or colon (right), respectively. Figure 1