Clonogenic assays have been established in hematology for 30 years. They ha
ve been widely used in fundamental studies on hematopoiesis and they are al
so routinely used in clinical hematology to confirm diagnosis or to predict
time to recovery in cases of bone marrow failure. Their use in toxicologic
al studies is more recent. Adverse effects of xenobiotics can induce hemato
logical problems and pathologies such as neutropenia, thrombocytopenia, ane
mia, and aplastic anemia. Three clonogenic assays are proposed for granulop
oiesis, megakaryopoieisis and erythropoieisis. Hematopoietic progenitors fr
om murine or human origin can be cultured in the presence of xenobiotics us
ing validated protocols to complete standard animal toxicological studies.
These clonogenic assays can help to predict adverse effects of drugs or tox
icants. Clonogenic assays using white blood cell progenitors (CFU-GM cultur
e) have recently been validated by ECVAM and can be used routinely. Megakar
yocyte progenitor (CFU-MK) culture is under development and prevalidation i
n toxicological studies supported by ECVAM. Red blood cells progenitor cult
ure (BFU-E) has been proposed but needs international validation to be reco
gnized.