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Separate tissues connect through adjoining basement membranes to carry out molecular barrier, exchange, and organ support functions. Cell adhesion at these connections must be robust and balanced to withstand independent tissue movement. Yet, how cells achieve synchronized adhesion to connect tissues is unknown. Here, we have investigated this question using the utse-seam tissue connection that supports the uterus during egg-laying. Through genetics, quantitative fluorescence, and cell-specific molecular disruption, we show that type IV collagen, which fastens the linkage, also activates the collagen receptor discoidin domain receptor-2 (DDR-2) in both the utse and seam. RNAi depletion, genome editing, and photobleaching experiments revealed that DDR-2 signals through LET-60/Ras to coordinately strengthen an integrin adhesion in the utse and seam that stabilizes their connection. These results uncover a synchronizing mechanism for robust adhesion during tissue connection, where collagen both affixes the linkage and signals to both tissues to bolster their adhesion.
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http://dx.doi.org/10.7554/eLife.87037 | DOI Listing |
Nat Commun
August 2025
Shanghai Frontiers Science Center of Drug Target Identification and Delivery, School of Pharmaceutical Sciences, Shanghai Jiao Tong University, Shanghai, China.
The clinical effectiveness of immunotherapies for lung cancers has been greatly hindered by the immune-excluded and immunosuppressive tumor microenvironment (TME) and limited pulmonary accessibility of therapeutics. Here, we develop an inhalable lipid nanoparticle (LNP) system that enables simultaneous delivery of mRNA encoding anti-discoidin domain receptor 1 (DDR1) single-chain variable fragments (mscFv) and siRNA targeting PD-L1 (siPD-L1) into pulmonary cancer cells. The secreted anti-DDR1 scFv blocks the binding of DDR1 extracellular domain to collagen, disrupting collagen fiber alignment and reducing tumor stiffness, thereby facilitating T cell infiltration.
View Article and Find Full Text PDFInt J Mol Sci
August 2025
School of Pharmacy & Laboratory of Drug Discovery from Natural Resources and Industrialization, Macau University of Science and Technology, Macau SAR, China.
Discoidin domain receptor 1 (DDR1), a collagen-binding receptor tyrosine kinase, plays a key role in extracellular matrix remodeling, tumor progression, and immune evasion. However, DDR1's comprehensive role across diverse cancers and its therapeutic potential in immune-resistant tumors remain poorly defined. We performed a pan-cancer analysis integrating bulk transcriptomic datasets, single-cell RNA sequencing, and pathway enrichment to evaluate expression, genetic alterations, and its associations with immune cell infiltration and clinical outcomes.
View Article and Find Full Text PDFJ Mol Med (Berl)
September 2025
Department of Biochemistry and Molecular Biology, School of Basic Medicine, Hebei Medical University, Shijiazhuang, Hebei Province, China, 050017.
The internalization of vascular endothelial growth factor receptor-2 (VEGFR-2) occurs in response to VEGF treatment, and it is eventually transported to the plasma membrane by several endosomes such as Rab5 and Rab11, which are responsible for transporting vesicles from the cytoplasm to plasma membrane. Therefore, the homeostasis of VEGFR-2 internalization and recycling is critical for maintaining the normality of the VEGF signaling pathway and regulates angiogenesis. Previous studies have shown that discoidin, CUB and LCCL domain containing 2 (DCBLD2) can promote the proliferation and migration of vascular endothelial cells (ECs) by promoting the VEGF signaling pathway, but the potential role of DCBLD2 on VEGFR-2 endocytosis remains unclear.
View Article and Find Full Text PDFHum Cell
August 2025
Department of Ear-Nose-Throat, The Second People's Hospital of Huai'an, Huai'an Affiliated Hospital of Xuzhou Medical University, No. 60, Huaihai South Road, Qingjiangpu District, Huai'an, 223000, Jiangsu, People's Republic of China.
The expression of collagen receptors by cancer cells serves a vital function in the regulation of cell behavior. These receptors are capable of sensing the signals generated by alterations in the collagen state, thereby contributing to the maintenance of cellular homeostasis. The discoidin domain receptor (DDR)1 functions as a critical sensor of collagen fiber state and composition, regulating tumor cell growth, response to therapy, and patient survival.
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
Department of Gastroenterology, The Second Hospital & Clinical Medical School, Lanzhou University, Lanzhou, Gansu Province, China. Electronic address:
Discoidin domain receptors (DDRs) are a family of tyrosine kinase transmembrane receptors composed of discoidin domain receptor 1 (DDR1) and discoidin domain receptor 2 (DDR2) that interact with components of the extracellular matrix. They are involved in a broad range of important physiological processes, such as extracellular matrix signaling, cell adhesion, cell migration, and tissue fibrosis. DDR1 and DDR2 are expressed in a variety of cell and tissue types, but their expression patterns are variable and dependent on receptor type and physiological environment.
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