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lüll Glucose-evoked alterations in connexin43-mediated cell-to-cell communication in human collecting duct: a possible role in diabetic nephropathy Hills CE; Bland R; Wheelans DC; Bennett J; Ronco PM; Squires PEAm J Physiol Renal Physiol 2006[Nov]; 291 (5): F1045-51Aberrant sodium absorption has been linked to the development of hypertension in both renal disease and diabetes. Efficient absorption depends on coordination of cellular activity across the entire epithelium via cell-to-cell coupling. In the current study we have utilized a model human collecting duct cell line (HCD) to assess the role of connexin43 (Cx43)-mediated gap junctions in the transfer of intracellular Ca(2+) transients within coupled cell clusters. HCD cells express Cx43 mRNA and protein, as well as that for the mechanosensitive transient receptor potential receptor (TRPV4). Mechanical stimulation of individual cells within a cluster evoked a transient rise in cytosolic Ca(2+) concentration ([Ca(2+)](i)) that propagated between cells via a heptanol-sensitive mechanism. The rise in [Ca(2+)](i) was dependent on both store release and Ca(2+)-influx pathways. Lucifer yellow dye transfer and Cx43 knockdown experiments confirmed direct cell-to-cell communication. Application of the Ca(2+) ionophore ionomycin, or an increase in glucose (5 to 25 mM), produced a time-dependent (48 h) increase in Cx43 protein expression. The transmission rate of touch-evoked Ca(2+) transients between coupled cells was accelerated after exposure to high glucose, providing a functional correlate to increased Cx43 expression. These data suggest a pivotal role for Cx43-mediated gap junctions in the synchronization of activity between HCD cells in response to stimuli that mimic osmotic and physical changes. Cx43 expression and cell-to-cell communication increased in response to high glucose and may protect the collecting duct from renal damage associated with more established diabetic nephropathy.|Calcium Signaling/drug effects/physiology[MESH]|Calcium/metabolism/pharmacology[MESH]|Cell Communication/drug effects/*physiology[MESH]|Cell Line, Transformed[MESH]|Connexin 43/genetics/*metabolism[MESH]|Diabetic Nephropathies/*metabolism/pathology/physiopathology[MESH]|Gap Junctions/metabolism[MESH]|Gene Expression/physiology[MESH]|Glucose/*metabolism/pharmacology[MESH]|Humans[MESH]|Hypertension, Renal/metabolism/pathology/physiopathology[MESH]|Kidney Tubules, Collecting/*cytology/*metabolism[MESH]|RNA, Messenger/metabolism[MESH]|RNA, Small Interfering[MESH]|TRPV Cation Channels/genetics/metabolism[MESH]|Up-Regulation[MESH] |