G proteins link many cell surface receptor generated signals to activa
tion of multiple cellular processes in all tissues. There is specifici
ty in the receptor interaction with the G protein and in the interacti
on of the specific G protein with different effector molecules. The pu
rpose of this study was to determine some of the biologically relevant
G proteins in keratinocytes. The Ga subunit of the heterotrimeric G p
rotein was investigated because much of the biologic activity and the
receptor specificity resides there. A polymerase chain reaction strate
gy was used that amplified multiple G alpha gene segments between cons
erved primer sites from keratinocyte first strand cDNA. Two Gq class G
proteins, G alpha 16 and G alpha y, were identified. Using northern a
nalysis and in situ hybridization, mRNA of both of these genes were de
tected in keratinocytes in culture and in epidermal keratinocytes. G a
lpha y was expressed in multiple other cell types and tissues, but G a
lpha 16 was restricted in expression to keratinocytes and keratinocyte
-derived adnexal structures in the skin. G alpha 16 has previously bee
n reported to be limited in expression to hematopoietic cells. The phy
siologic receptor to which it couples in neutrophils is reported to be
a C5a receptor. The receptor to which it couples in keratinocytes has
not been elucidated but by analogy may be another chemokine receptor.
We hypothesize that G alpha 16 is an important conduit for responses
to inflammatory signals in keratinocytes.