The potential for aquatic gastropods to display phenotypic plasticity in response to predator cues is well documented. However, long-term phenotypic responses to predator exposure are difficult to evaluate at large scales in the field. Thus, the extent to which comparatively dilute predator cues experienced by natural snail populations influence morphometric development and whether energetic costs associated with defensive morphology have allometric impacts on other life-history characteristics is unclear. The 2013 sea star wasting disease outbreak in central California, USA provided a unique framework for a large-scale natural predator removal experiment, comparing the shell morphometrics and gonadosomatic index of subtidal turban snail populations at kelp forest sites where local predatory sea stars were completely absent or nearly so (SS-), with paired sites maintaining low predator densities (SS+). All three snail species displayed higher proportional allocation to shell mass at SS+ locations and concomitantly higher reproductive allocation with predators absent (SS-). Dietary stable isotope analysis suggests this may be partially an energetic consequence of behavioural grazing shifts displayed by snails following predator release. Interestingly, morphometric shifts in shell structure differed among the three species and appeared closely related to species-specific predator avoidance strategies.
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http://dx.doi.org/10.1098/rspb.2024.1378 | DOI Listing |
Geroscience
January 2025
Buck Institute for Research On Aging, Novato, CA, 94945, USA.
Cells are subjected to dynamic mechanical environments which impart forces and induce cellular responses. In age-related conditions like pulmonary fibrosis, there is both an increase in tissue stiffness and an accumulation of senescent cells. While senescent cells produce a senescence-associated secretory phenotype (SASP), the impact of physical stimuli on both cellular senescence and the SASP is not well understood.
View Article and Find Full Text PDFClin Exp Med
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Department of Thoracic Surgery, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, China.
Introduction Recently, immune cells within the tumor microenvironment (TME) have become crucial in regulating cancer progression and treatment responses. The dynamic interactions between tumors and immune cells are emerging as a promising strategy to activate the host's immune system against various cancers. The development and progression of hepatocellular carcinoma (HCC) involve complex biological processes, with the role of the TME and tumor phenotypes still not fully understood.
View Article and Find Full Text PDFCell Mol Life Sci
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Department of Oncology, The Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Hypoxia, or a state of low tissue oxygenation, has been characterized as an important feature of solid tumors that is related to aggressive phenotypes. The cellular response to hypoxia is controlled by Hypoxia-inducible factors (HIFs), a family of transcription factors. HIFs promote the transcription of gene products that play a role in tumor progression including proliferation, angiogenesis, metastasis, and drug resistance.
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Department of Cardiothoracic Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.
Background: Esophageal squamous cell carcinoma (ESCC) is one of the most prevalent and lethal malignancies worldwide. Despite progress in immunotherapy for cancer treatment, its application and efficacy in ESCC remain limited. Therefore, there is an ongoing need to explore potential molecules and therapeutic strategies related to tumor immunity in ESCC.
View Article and Find Full Text PDFBMC Public Health
January 2025
Department of Dermatology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Background: Chronic respiratory diseases (CRD) represents a series of lung disorders and is posing a global health burden. Systemic inflammation and phenotypic ageing have been respectively reported to associate with certain CRD. However, little is known about the co-exposures and mutual associations of inflammation and ageing with CRD.
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