We are studying how immune responses affect tissue function with the aim to devise countermeasures.

While several perturbations (e.g., allergens, pathogens, dietary factors, self-reactive immune cells) are restricted in their direct cellular targets, they can still radically impact non-target cells via the inflammation they induce. In some cases, this alters overall tissue structure and function, and results in chronic diseases that can persist even after the original perturbation is contained or eliminated, limiting the efficacy of current intervention strategies. We aim to identify how immune and non-immune tissue-resident cellular subsets participate in inflammation and its memory, as well as how these responses affect tissue function across disease contexts. Our goal is to develop a working knowledge of biological memory across scales (e.g., cellular-level, tissue-level) so that we can overwrite it to restore tissue health or leverage it to enhance resilience.

Highlights

Hepatic adaptation to chronic metabolic stress primes tumorigenesis

Tzouanas et al., Cell, 2026

During chronic stress, cells must support both tissue function and their own survival. Hepatocytes perform metabolic, synthetic, and detoxification roles, but chronic nutrient imbalances can induce hepatocyte death and precipitate metabolic dysfunction-associated steatohepatitis (MASH, formerly NASH). Despite prior work identifying stress-induced drivers of hepatocyte death, chronic stress’ functional impact on surviving cells remains unclear. Through cross-species longitudinal single-cell multi-omics, we show that ongoing stress drives prognostic developmental and cancer-associated programs in non-transformed hepatocytes while reducing their mature functional identity. Creating integrative computational methods, we identify and then experimentally validate master […]