Fetal programming · Aging · Senescence

The beginning of life can shape the way we age.

We investigate how conditions during gestation program molecular mechanisms that accelerate cellular senescence and increase susceptibility to chronic disease.

Approach
Life course
Scale
From cell to organism
Purpose
Prevent future disease
ProgrammingSenescenceAging
FetalAge Lab

Fetal Programming, Aging & Cellular Senescence

Our question

A trajectory that begins before birth.

We connect gestational signals to cellular mechanisms and health outcomes that emerge years later.

01

Gestational environment

Hypoxia, nutrition, and other early signals shape the developmental trajectory.

02

Molecular programming

Epigenetic, metabolic, and mitochondrial changes persist after birth.

03

Cellular senescence

We study cell-cycle arrest, damage, inflammation, and the SASP secretory phenotype.

04

Biological aging

We link early-life mechanisms to organ dysfunction and chronic disease.

Research areas

Developmental biology through a life-course lens.

Our laboratory integrates physiology, molecular biology, and omics to understand the early origins of aging.

01DOHaD

Fetal programming

How adverse exposures during gestation alter development and future health.

02SASP

Cellular senescence

Mechanisms driving the accumulation of senescent cells and their inflammatory signaling.

03AGE

Systemic aging

Liver, metabolic, vascular, and brain aging trajectories across the life course.

04OMICS

Epigenetics and transcriptomics

Molecular signatures linking the prenatal environment to persistent offspring phenotypes.

Fondecyt Initiation Grant No. 11261218 · ANID

The fetal dilemma and accelerated liver senescence.

We study whether adverse prenatal exposure induces early hepatocyte senescence, a persistent SASP phenotype, and greater metabolic vulnerability in adulthood.

ModelGuinea pig
WindowGestation → adulthood
IntegrationFunction · Histology · Omics
View experimental approach

How we investigate

From integrative physiology to molecular signatures.

We combine experimental models and multiscale analyses to examine the same phenomenon from the whole organism to genes and proteins.

01Gestational hypoxia models02Molecular biology03Histology and immunodetection04Mitochondrial bioenergetics05RNA-seq and pathway analysis06Senescence biomarkers07Oxidative stress08Integrative physiology
Dr. Esteban Gabriel Figueroa Becerra, principal investigator of FetalAge Lab
Santiago · Chile

Principal investigator

Dr. Esteban Gabriel Figueroa Becerra

Engineer and MSc in Biotechnology from Universidad Andrés Bello, PhD in Nanosciences specializing in Nanopharmacotherapy from the University of Barcelona, with postdoctoral training at Universidad de O'Higgins.

He is currently a faculty researcher at the School of Midwifery, Universidad San Sebastián, and principal investigator of Fondecyt Initiation Grant No. 11261218. His work connects fetal programming, gestational hypoxia, oxidative stress, and cellular senescence to study the early origins of chronic disease.

Training
Biotechnology · Nanosciences
Affiliation
Universidad San Sebastián
ORCID
0000-0003-1316-738X
Scientific network
USSUOHUniversidad de ChileTranslational medicine
From left to right: Amanda Albornoz, Belén Pino, and Vanesa Uribe, fourth-year Midwifery students at Universidad San Sebastián

Research training

Student interns

Amanda Albornoz, Belén Pino, and Vanesa Uribe, fourth-year Midwifery students at Universidad San Sebastián.

  1. 01Amanda Albornoz
  2. 02Belén Pino
  3. 03Vanesa Uribe

Let's connect

Interested in research, a thesis, or collaboration?

FetalAge Lab is building a network to study the early origins of aging and chronic disease.

Email the laboratory