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 Transport pathways for cadmium in the intestine and kidney proximal tubule: focus  on the interaction with essential metals Vesey DAToxicol Lett  2010[Sep]; 198 (1): 13-9Cadmium (Cd) is a toxic metal with a propensity to accumulate in the proximal  tubules cells (PTC) of the kidney where it can lead to tubular dysfunction and  eventually renal failure. Although Cd(2+)-induced nephrotoxicity has been well  described there is still uncertainty about how this metal gains entry into these  cells to induce toxicity. As a non-essential metal, specific transport proteins  for Cd are unlikely to exist. Rather transport proteins/channels used by  essential metals (iron, zinc, calcium) are thought to be responsible. When these  dietary essential metals are in short supply and deficiencies develop, Cd  absorption and toxicity are enhanced. This is primarily due to increased  expression of essential metal transport proteins such as divalent metal  transporter 1 (DMT1) which can transport Cd in the intestine and enhance toxicity  in the kidney. The zinc/bicarbonate sympoters ZIP8 and 14 are expressed at the  apical membrane of enterocytes and PTC, and can transport Cd into cells. TRPV5  and 6 are major transporters for calcium in intestine and kidney and may be  involved in Cd transport in these locations. Cd in the circulation is bound to  proteins such as metallothioneins (MT) which are readily filtered. Two  multiligand receptors, megalin and cubulin, reabsorb filtered proteins including  albumin and MT by the process of receptor-mediated endocytosis. This review  summarises the transport pathways for Cd in the intestine and kidney proximal  tubule focusing in particular at how Cd uses essential metal transport processes  to gain entry to the circulation and the kidney.|Cadmium/chemistry/*pharmacokinetics/toxicity[MESH]|Calcium/chemistry/metabolism[MESH]|Hazardous Substances/*pharmacokinetics/toxicity[MESH]|Intestinal Mucosa/*metabolism[MESH]|Intestines/drug effects[MESH]|Iron/chemistry/metabolism[MESH]|Kidney Tubules, Proximal/drug effects/*metabolism[MESH]|Metallothionein/metabolism[MESH]|Zinc/chemistry/metabolism[MESH]
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