The Library
Glucose-evoked alterations in connexin43-mediated cell-to-cell communication in human collecting duct: a possible role in diabetic nephropathy
Tools
Tools
Tools
Hills, Claire E., Bland, Rosemary, Wheelans, Dianne C., Bennett, Jeanette, Ronco, Pierre M. and Squires, Paul E. (2006) Glucose-evoked alterations in connexin43-mediated cell-to-cell communication in human collecting duct: a possible role in diabetic nephropathy. AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 291 (5). F1045-F1051. doi:10.1152/ajprenal.00344.2005 ISSN 0363-6127.
Research output not available from this repository.
Request-a-Copy directly from author or use local Library Get it For Me service.
Official URL: http://dx.doi.org/10.1152/ajprenal.00344.2005
Abstract
Aberrant 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 Ca2+ 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 Ca2+ concentration ([Ca2+](i)) that propagated between cells via a heptanol-sensitive mechanism. The rise in ([Ca2+](i)) was dependent on both store release and Ca2+-influx pathways. Lucifer yellow dye transfer and Cx43 knockdown experiments confirmed direct cell-to-cell communication. Application of the Ca2+ 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 Ca2+ 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.
| Item Type: | Journal Article | ||||
|---|---|---|---|---|---|
| Subjects: | Q Science > QP Physiology R Medicine > RC Internal medicine |
||||
| Journal or Publication Title: | AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY | ||||
| Publisher: | AMER PHYSIOLOGICAL SOC | ||||
| ISSN: | 0363-6127 | ||||
| Official Date: | November 2006 | ||||
| Dates: |
|
||||
| Volume: | 291 | ||||
| Number: | 5 | ||||
| Number of Pages: | 7 | ||||
| Page Range: | F1045-F1051 | ||||
| DOI: | 10.1152/ajprenal.00344.2005 | ||||
| Publication Status: | Published |
Data sourced from Thomson Reuters' Web of Knowledge
Request changes or add full text files to a record
Repository staff actions (login required)
 |
View Item |
