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Naked-mole rats (NMRs; ) exhibit unique biological traits such as resistance to cancer, exceptional longevity, and high tolerance to low-oxygen environments. However, little is known about the lung structure of this eusocial species. Here, the lungs of adult NMRs were qualitatively examined using light and electron microscopy, followed by structural quantification of the alveolar region by means of stereology. One queen (>18 years) was also included in the study. The data normalized to body weight (BW) were furthermore compared to that of young and old mice () as well as the expression of genes of surfactant proteins. Qualitatively, NMRs showed larger conducting airways compared to mice. Additionally, alveolar septa with a double-layered capillary network were observed in NMRs, indicating microvascular maturation and late alveolarization. Stereological analysis of the lung parenchyma revealed a lower septal surface area and alveolar epithelial type II (AEII) cell number per BW in NMRs compared to mice. However, in NMRs, the AEII cells were larger with a higher content of lamellar bodies, resulting in more intracellular surfactant per BW. Furthermore, the expression of surfactant protein B () was prominently higher in NMRs. The queen showed a larger mean alveolar volume, but no other age-related structural alterations were observed. The results indicate that NMRs are capable of late alveolarization, which is in line with their good regenerative potential. Additionally, NMRs have more intracellular surfactant and higher expression of , suggesting functional alterations in their surfactant system possibly as an environmental adaptation. Naked mole-rats (NMRs) can adapt to hypoxic environments and are the longest-living rodents. Comparison of their lung structure with that of mice revealed that NMRs have a reduced alveolar surface area per body weight but an increased pool of intracellular surfactant. Additionally, the septa of NMRs were thicker with an occasional double-layered capillary network. These features indicate a high regenerative potential with late alveolarization and environmental adaptation, even in old animals (>18 years).
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http://dx.doi.org/10.1152/ajplung.00246.2024 | DOI Listing |
Nat Mater
September 2025
Department of Materials Science and Engineering, University of Michigan, Ann Arbor, MI, USA.
Within most tissues, the extracellular microenvironment provides mechanical cues that guide cell fate and function. Changes in the extracellular matrix such as aberrant deposition, densification and increased crosslinking are hallmarks of late-stage fibrotic diseases that often lead to organ dysfunction. Biomaterials have been widely used to mimic the mechanical properties of the fibrotic matrix and study pathophysiologic cell function.
View Article and Find Full Text PDFShanghai Kou Qiang Yi Xue
June 2025
Department of Stomatology, Fourth Affiliated Hospital of Nanchang University. Nanchang 330003, Jiangxi Province, China. E-mail:
Purpose: To evaluate the clinical efficacy of immediate replantation using simple taper fixed implants at failed implantation sites.
Methods: Patients with implant failure at the Department of Stomatology, Fourth Affiliated Hospital of Nanchang University from January 2018 to December 2022 were collected. Simple taper-retained implants were used for immediate replantation at implant failure sites.
Dev Cell
August 2025
Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Guangdong-Hong Kong Joint Laboratory for RNA Medicine, Breast Tumor Center, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou 510120, China; State Key Laboratory of Oncology in South China, Sun Yat
Tumor-antigen-specific CD8 T cells (CTLs) are the main effector immunocytes in anti-tumor immunity, but their systemic deployment against cancer metastasis remains uncharacterized. Here, we found that the abundance of tumor-specific CD103CD8 T cells in the tumor-draining lymph nodes (TDLNs) was associated with improved lung-metastasis-free survival in breast cancer patients. In mouse cancer models, CD103CD8 T cells were primed in TDLNs and recruited to the lungs via C-C motif chemokine ligand 5/receptor 9 (CCL25/CCR9) signaling to inhibit metastasis through antigen-specific immunity.
View Article and Find Full Text PDFAm J Transplant
August 2025
Departments of Surgery, St. Louis, MO, USA; Departments of Pathology & Immunology, St. Louis, MO, USA. Electronic address:
Tolerance after lung transplantation is associated with the induction of Foxp3 regulatory T cell-enriched bronchus-associated lymphoid tissue, which suppresses local and systemic alloimmune responses. How this tolerogenic graft environment shapes responses to respiratory viral infections, a known contributor to adverse outcomes after lung transplantation, remains unknown. Using a mouse model of a seasonally circulating parainfluenza virus, we found that acute infection of tolerant lung allografts results in temporary reductions of both bronchus-associated lymphoid tissue size and abundance of graft-resident Foxp3 cells, but doesn't trigger rejection.
View Article and Find Full Text PDFRespir Res
August 2025
Department of Pediatrics, University of Utah, Salt Lake City, UT, USA.
Background: AVR-48 is a small molecule that modulates toll-like receptor 4 (TLR4) activity, changing macrophage phenotype from pro- to anti-inflammatory and increasing the anti-inflammatory cytokine IL-10. Treatment with AVR-48 via intraperitoneal injection effectively prevented hyperoxia-induced pathology in a newborn mouse model of bronchopulmonary dysplasia (BPD).
Objective: To evaluate the early and late-stage efficacy of AVR-48 in preventing BPD and associated complications in a mechanically ventilated preterm lamb model that mimics human BPD.