TY - JOUR
T1 - A secreted cell number counting factor represses intracellular glucose levels to regulate group size in Dictyostelium
AU - Jang, Wonhee
AU - Chiem, Binh
AU - Gomer, Richard H.
PY - 2002/10/18
Y1 - 2002/10/18
N2 - Developing Dictyostelium cells form evenly sized groups of ∼2 × 10 4 cells. A secreted 450-kDa protein complex called counting factor (CF) regulates group size by repressing cell-cell adhesion and myosin polymerization and by increasing cAMP-stimulated cAMP production, actin polymerization, and cell motility. We find that CF regulates group size in part by repressing internal glucose levels. Transformants lacking bioactive CF and wild-type cells with extracellular CF depleted by antibodies have high glucose levels, whereas transformants oversecreting CF have low glucose levels. A component of CF, countin, affects group size in a manner similar to CF, and a 1-min exposure of cells to countin decreases glucose levels. Adding 1 mM exogenous glucose negates the effect of high levels of extracellular CF on group size and mimics the effect of depleting CF on glucose levels, cell-cell adhesion, cAMP pulse size, actin polymerization, myosin assembly, and motility. These results suggest that glucose is a downstream component in part of the CF signaling pathway and may be relevant to the observed role of the insulin pathway in tissue size regulation in higher eukaryotes.
AB - Developing Dictyostelium cells form evenly sized groups of ∼2 × 10 4 cells. A secreted 450-kDa protein complex called counting factor (CF) regulates group size by repressing cell-cell adhesion and myosin polymerization and by increasing cAMP-stimulated cAMP production, actin polymerization, and cell motility. We find that CF regulates group size in part by repressing internal glucose levels. Transformants lacking bioactive CF and wild-type cells with extracellular CF depleted by antibodies have high glucose levels, whereas transformants oversecreting CF have low glucose levels. A component of CF, countin, affects group size in a manner similar to CF, and a 1-min exposure of cells to countin decreases glucose levels. Adding 1 mM exogenous glucose negates the effect of high levels of extracellular CF on group size and mimics the effect of depleting CF on glucose levels, cell-cell adhesion, cAMP pulse size, actin polymerization, myosin assembly, and motility. These results suggest that glucose is a downstream component in part of the CF signaling pathway and may be relevant to the observed role of the insulin pathway in tissue size regulation in higher eukaryotes.
UR - http://www.scopus.com/inward/record.url?scp=0037131247&partnerID=8YFLogxK
U2 - 10.1074/jbc.M205635200
DO - 10.1074/jbc.M205635200
M3 - Article
C2 - 12161440
AN - SCOPUS:0037131247
SN - 0021-9258
VL - 277
SP - 39202
EP - 39208
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 42
ER -