
Heterochronic myeloid cell replacement reveals the local brain environment as key driver of microglia aging ↗
Young replacement microglia, the brain's immune cells, aged fast in old brains. Old ones looked young in young brains.
From the brain, into the dish, and back into the brain: genome-wide CRISPR screens, Perturb-seq, Cell Painting, in vivo immune cell replacement, and 2-photon imaging.

Young replacement microglia, the brain's immune cells, aged fast in old brains. Old ones looked young in young brains.

We profiled 15 mouse brain regions across 7 ages. Glial aging runs faster in white matter than cortex.

CoolMPS sequencing reproduced standard Illumina results on single-nucleus RNA from young and old mouse hippocampus.

Organs hit the same aging hallmarks on different schedules. Immune activation shows first in white fat.

In 800 mice, stopping dietary restriction at 24 months raised mortality fast. Starting it late helped only weakly.

Dietary restriction, rapamycin and dwarf genetics each add methylation inside gene bodies in mouse liver.

Dietary restriction delayed age-related epigenetic changes in mouse liver and added methylation at lipid genes.

A microRNA atlas of 15 mouse brain regions. miR-155-5p rises with age in both sexes, driven by microglia.

Replacing immune cells by transplant improved neurological deficits in a mouse model of multiple sclerosis.

A noncoding RNA map of 16 organs. miR-29c-3p tracks aging and returns to young levels in liver with young blood.

RNA polymerase speeds up with age in five species. Dietary restriction reverses most of this, and slowing polymerase extends lifespan.

Klotho raises platelet factors in blood. One of them, PF4, improves cognition in young and old mice.

Young cerebrospinal fluid improved memory in old mice. Fgf17 alone did too.

Plasma from running mice reduced brain inflammation in sedentary mice, through proteins including clusterin.

Brains from COVID-19 patients showed no molecular trace of virus but broad changes in barrier cells and microglia.

Microglia fill with lipid droplets as brains age. These cells clear debris poorly and drive inflammation.

A single-cell atlas of aging across 23 mouse tissues and organs.

Mice that lost smell neurons resisted diet-induced obesity. Losing smell after obesity reduced fat mass.

A community challenge scored over 2,000 networks for causal links in cancer cell signaling.