Human corpora lutea undergo an extremely rapid period of growth, developmen
t and regression during the course of non-fertile cycles. The tissue consis
ts of steroidogenic (parenchymal) and non-steroidogenic (stromal) cells. In
women and other primates, steroid hormone production by corpora lutea depe
nds on the presence of pituitary-derived LH. Nevertheless, there is also in
tra-luteal regulation of steroid synthesis. Steroidogenic luteal cells and
non-steroidogenic cells interact via endocrine and paracrine pathways, and
by contact-dependent pathways (gap junctions). Thus, hormones and locally p
roduced factors including steroids, growth factors, cytokines, reactive oxy
gen species and nitric oxide may modulate luteal lifespan. The factors regu
lating regression and rescue of the corpus luteum are not understood comple
tely. This review describes the expression of two representative intragonad
al peptides that may influence luteal regression (interleukin 1 beta) and l
uteal rescue (steroidogenic acute regulatory protein).