We are defining what influences homeostasis, or balance, across scales in order to improve resilience.

We are exposed to a constant flux of external biochemical and physical stimuli. Despite variability in overall experience and exact constitution, our individual tissues typically manage to maintain functionality, though each can differ in its resilience to distinct stressors. We aim to understand how differences in cellular composition and communication impact tissue fitness, and identify responses and subsequent adaptations that drive chronic dysfunction.

We are also investigating how tissue-resident cellular subsets participate in, and are shaped by, environmental exposures at barrier tissues, and the functional consequences of these experiences. Our goal is to develop a more holistic appreciation for how different intra- and extracellular factors (e.g., genetics and integrated exposure history, respectively) influence barrier tissue function.

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 […]