The objective of the present study was to determine the expression of MT-3
in the human kidney. To accomplish this, an antibody was generated against
a unique 8 amino acid sequence present in MT-3 that is not shared by any ot
her MT family member. Western analysis demonstrated that the resulting anti
body reacted with a protein band of approximately 6 kDa, corresponding to t
he known molecular weight of MT-3. Immunohistochemical staining using this
antibody demonstrated reactivity with several epithelial components of the
nephron. In the glomerulus, moderate intensity was demonstrated in parietal
epithelial cells of Bowman's capsule and in visceral epithelial cells of t
he glomerular tuft. Proximal convoluted tubule cells exhibited moderate cyt
oplasmic MT-3 reactivity. Distal tubules showed strong cytoplasmic staining
for MT-3, particularly in the medullary rays. In the medulla, MT-3 stainin
g was the most variable, with weak to moderate staining in the medullary co
llecting ducts and a general absence of staining in the thin loops of Henle
and in the transitional epithelium of the renal pelvis. The finding that M
T-3 is constitutively expressed in several glomerular and tubular epithelia
l elements of the human kidney warrants consideration of an expanded role f
or this protein family in maintaining renal homeostasis. (C) 1999 Elsevier
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