TY - JOUR
T1 - Expression of SLC4A11 protein in mouse and rat medulla
T2 - a candidate transporter involved in outer medullary ammonia recycling
AU - Gee, Michael T.
AU - Kurtz, Ira
AU - Pannabecker, Thomas L.
N1 - Funding Information:
Supported by the National Institutes of Health: National Institute of Diabetes and Digestive and Kidney Diseases, grants DK083338 (T. L. P.), Joint DMS/NIGMS Initiative under NSF grant DMS-1263943 (T. L. P.). (I.K.) is supported in part by funds from the NIH National Institute of Diabetes and Digestive and Kidney Diseases (DK077162), the Allan Smidt Charitable Fund, the Factor Family Foundation and the Ralph Block Family Foundation.
Publisher Copyright:
© 2019 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society.
PY - 2019/5
Y1 - 2019/5
N2 - SLC4A11 is a multifunctional membrane transporter involved with H+ transport, NH3 and alkaline pH stimulated H+ transport, and water transport. The role of SLC4A11 in the kidney is not well understood. A prior study has shown that in murine kidney, SLC4A11/LacZ staining is primarily in the long-looped descending thin limb (DTL) as determined by colocalization with aquaporin 1 (AQP1), a protein that is expressed in some, but not all, descending thin limb segments. Using a previously characterized polyclonal antibody, we demonstrate the selective expression of SLC4A11 in the upper DTLs (which are AQP1-positive) in the outer medulla and inner medulla with little or no expression in the lower DTLs (which are AQP-1-null). SLC4A11 also colocalized with AQP1 and the urea transporter UT-B in the mouse descending vasa recta, but was absent in mouse and rat ascending vasa recta. Mouse, but not rat, outer medullary collecting duct cells also labeled for SLC4A11. Our results are compatible with the hypothesis that in the inner stripe of the outer medulla, SLC4A11 plays a role in the countercurrent transport of ammonia absorbed from the outer medullary thick ascending limb and secreted into the long-looped DTLs. SLC4A11 can potentially modulate the rate of ammonia transport in the mouse outer medullary collecting duct. Our data suggest functionally unique SLC4A11 pathways in mouse and rat and complement previous studies of DTL Na+, urea and water permeability indicating that the upper and lower DTLs of long-looped nephrons are functionally distinct.
AB - SLC4A11 is a multifunctional membrane transporter involved with H+ transport, NH3 and alkaline pH stimulated H+ transport, and water transport. The role of SLC4A11 in the kidney is not well understood. A prior study has shown that in murine kidney, SLC4A11/LacZ staining is primarily in the long-looped descending thin limb (DTL) as determined by colocalization with aquaporin 1 (AQP1), a protein that is expressed in some, but not all, descending thin limb segments. Using a previously characterized polyclonal antibody, we demonstrate the selective expression of SLC4A11 in the upper DTLs (which are AQP1-positive) in the outer medulla and inner medulla with little or no expression in the lower DTLs (which are AQP-1-null). SLC4A11 also colocalized with AQP1 and the urea transporter UT-B in the mouse descending vasa recta, but was absent in mouse and rat ascending vasa recta. Mouse, but not rat, outer medullary collecting duct cells also labeled for SLC4A11. Our results are compatible with the hypothesis that in the inner stripe of the outer medulla, SLC4A11 plays a role in the countercurrent transport of ammonia absorbed from the outer medullary thick ascending limb and secreted into the long-looped DTLs. SLC4A11 can potentially modulate the rate of ammonia transport in the mouse outer medullary collecting duct. Our data suggest functionally unique SLC4A11 pathways in mouse and rat and complement previous studies of DTL Na+, urea and water permeability indicating that the upper and lower DTLs of long-looped nephrons are functionally distinct.
KW - Countercurrent mechanism
KW - H transport
KW - thin limb of Henle's loop
KW - vasa recta
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U2 - 10.14814/phy2.14089
DO - 10.14814/phy2.14089
M3 - Article
C2 - 31124301
AN - SCOPUS:85066475526
SN - 2051-817X
VL - 7
JO - Physiological reports
JF - Physiological reports
IS - 10
M1 - e14089
ER -