Modulation of gene expression through altered transcription regulates stell
ate cell behavior in normal liver and following hepatic injury. Transcripti
on factors are generally classified according to conserved motifs within ei
ther the activation- or DNA-binding domains of the molecules. Transcription
al activity in stellate cells represents a delicate fine tuning of multiple
inputs. Activities of these transcription factors are modified by their in
tracellular localization, rate and pathway of degradation, oligomerization,
and interactions with heterologous factors and chromatin, as well as by po
sttranslational modifications, including phosphorylation, glycosylation, an
d acetylation. General paradigms of transcriptional control are increasingl
y being validated in hepatic stellate cells, particularly involving the tra
nscription factors CCAAT/enhancer-binding proteins, c-myb, CREB, nuclear fa
ctor kappaB, peroxisome proliferator-activated receptor, and Kruppel-like z
inc finger factors. Although there are no simple rules that govern mechanis
ms of transcriptional regulation in stellate cells, continued advances win
yield new insights into their role in normal liver homeostasis and in the r
esponse to injury.