Type 2 diabetes (T2D) is marked by insulin resistance together with the progressive failure of pancreatic β-cells. Increasing evidence suggests that this failure is shaped not only by β-cells themselves, but also by the local islet immune microenvironment, where resident and recruited macrophages can influence inflammation, islet architecture, and insulin secretion. Exercise is a cornerstone of diabetes management, yet how it acts within this islet microenvironment has remained unclear.

Ependymoma is a central nervous system tumor that occurs primarily in children and can arise in the supratentorial region, posterior fossa, or spinal cord. Although molecular classification has substantially improved disease stratification and prognostic assessment, the metabolic phenotypes associated with the major pediatric subtypes have remained poorly defined. Because pediatric ependymoma is rare, assembling a cohort that spans multiple molecularly defined subtypes for systematic metabolic comparison is itself challenging.

A robust method has been developed for producing human trophoblast stem cells (hTSCs) from late-gestation placentas, opening a new avenue for studying pregnancy complications using patient-derived cells.

Diabetes is a highly prevalent chronic condition and a major contributor to the global burden of disease, posing substantial challenges to health systems. Cardiovascular disease (CVD) remains its leading complication, and people with diabetes face a two- to four-fold higher risk of cardiovascular morbidity and mortality than the general population. Control of glycated hemoglobin (HbA1c), blood pressure, and low-density lipoprotein cholesterol (LDL-C), collectively referred to as ABC risk factors, is a cornerstone of cardiovascular prevention in diabetes.

Lysosomes were once viewed mainly as cellular waste disposers, but are now recognized as key hubs for nutrient sensing and metabolic signaling. Still, what lysosomes contribute metabolically inside high-demand neurons in the intact brain remains elusive.

Polycystic ovary syndrome (PCOS) affects 6%−20% of reproductive-aged women, and is commonly accompanied by irregular menstrual cycles and anovulatory infertility. The mechanisms underlying menstrual cycle irregularities associated with PCOS, and how they may change after pregnancy remain incompletely understood.

The intestinal epithelium undergoes rapid renewal every 3–5 days, a process driven by intestinal stem cells (ISCs) located at the base of crypts. While ISCs play an essential role in epithelial regeneration following injury, such as that induced by chemotherapy or radiation, the underlying regulatory mechanisms remain incompletely understood.

A peer-reviewed narrative review published in Brain Medicine draws anthropology, archival history, and comparative genomics into a single frame in order to reassess what industrialization actually did to human sleep. Field data from three hunter-gatherer societies place nightly sleep at roughly 6.4 to 7.1 hours, similar to or shorter than industrialized averages, which shifts the argument away from duration and toward timing, regularity, and circadian alignment. The synthesis reconsiders the segmented sleep hypothesis, follows conserved regulators such as DEC2 and hypocretin across lineages, and reviews evidence that urban noise, light, heat, and housing distribute sleep health unequally. Split sleep remains untested.

For decades, scientists have understood proteins primarily through two defining features: their amino acid sequence and their three-dimensional structure. This framework has driven major advances in biology, biotechnology, and medicine, culminating in recent artificial intelligence tools capable of predicting protein structures with remarkable accuracy. Yet a fundamental challenge remains: even when a protein's sequence and structure are known, predicting its function, interactions, and behavior often remains difficult. An international team of researchers from Japan, Finland, Italy, and the United States now reports evidence that part of this missing information may lie in an often-overlooked component of proteins: the highly organized water surrounding them. In a study accepted for publication in Nature Communications, the team provides the first direct three-dimensional visualization of sequence-dependent hydration architectures surrounding peptide assemblies at sub-nanometer resolution using advanced three-dimensional atomic force microscopy (3D-AFM). The findings reveal that water near peptide and protein surfaces is not simply a passive solvent. Instead, it forms highly organized, multilayered structures whose organization is dictated by the underlying amino acid sequence and surface chemistry. These hydration architectures extend multiple layers from the peptide surface and contain distinct structural signatures associated with hydrophobic, polar, aromatic, and charged amino acid residues.