Gap junctions enable intercellular communication and play an important
role in a variety of vital cellular functions including differentiati
on and the control of growth, These junctions are formed by a hexameri
c of proteins known as connexins. We investigated the distribution of
the connexin 43 (Cx43) gap junction protein in renal cells and human k
idney using the all;aline phosphatase anti-alkaline phosphatase immuno
histochemical technique with a monoclonal antibody directed against th
e cytoplasmic domain of this antigen, Strong staining was demonstrated
on the vascular endothelium, the smooth muscle of larger vessels and
on glomerular epithelial cells. In addition, Cx43 was expressed on pro
ximal tubular cells, glomerular endothelial cells and occasional cells
infiltrating the interstitium. In areas of tubular atrophy there was
increased staining for Cx43. Using reverse transcription-polymerase ch
ain reaction we have also demonstrated that cultured human and rat mes
angial cells and human proximal tubular cells express Cx43 messenger R
NA. In summary, we have described for the first time the distribution
of Cx43 in human kidney and cultured renal cells.