Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1999-4-13
pubmed:abstractText
It has been controversial whether high water permeability in the thin descending limb of Henle (TDLH) is required for formation of a concentrated urine by the kidney. Freeze-fracture electron microscopy (FFEM) of rat TDLH has shown an exceptionally high density of intramembrane particles (IMPs), which were proposed to consist of tetramers of aquaporin-1 (AQP1) water channels. In this study, transepithelial osmotic water permeability (Pf) was measured in isolated perfused segments (0.5-1 mm) of TDLH in wild-type (+/+), AQP1 heterozygous (+/-), and AQP1 null (-/-) mice. Pf was measured at 37 degrees C using a 100 mM bath-to-lumen osmotic gradient of raffinose, and fluorescein isothiocyanate (FITC)-dextran as the luminal volume marker. Pf was (in cm/s): 0.26 +/- 0.02 ([+/+]; SE, n = 9 tubules), 0.21 +/- 0.01 ([+/-]; n = 12), and 0.031 +/- 0.007 ([-/-]; n = 6) (P < 0.02, [+/+] vs. [+/-]; P < 0.0001, [+/+] vs. [-/-]). FFEM of kidney medulla showed remarkably fewer IMPs in TDLH from (-/-) vs. (+/+) and (+/-) mice. IMP densities were (in microm-2, SD, 5-12 micrographs): 5,880 +/- 238 (+/+); 5,780 +/- 450 (+/-); and 877 +/- 420 (-/-). IMP size distribution analysis revealed mean IMP diameters of 8.4 nm ([+/+] and [+/-]) and 5.2 nm ([-/-]). These results demonstrate that AQP1 is the principal water channel in TDLH and support the view that osmotic equilibration along TDLH by water transport plays a key role in the renal countercurrent concentrating mechanism. The similar Pf and AQP1 expression in TDLH of (+/+) and (+/-) mice was an unexpected finding that probably accounts for the unimpaired urinary concentrating ability in (+/-) mice.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-1186121, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-1282299, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-14141447, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-1415570, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-1526967, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-1621821, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-1700184, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-3550226, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-4427417, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-6660295, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-7028660, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-7388918, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-7395995, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-7529263, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-7541952, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-7678419, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-7693713, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-7694481, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-7733325, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-8421053, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-8772426, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-8812490, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-9176377, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-9195910, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-9468475, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-9486146, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-9501203, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-9545259, http://linkedlifedata.com/resource/pubmed/commentcorrection/10021457-9689137
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0021-9738
pubmed:author
pubmed:issnType
Print
pubmed:volume
103
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
491-6
pubmed:dateRevised
2011-10-7
pubmed:meshHeading
pubmed:year
1999
pubmed:articleTitle
Reduced water permeability and altered ultrastructure in thin descending limb of Henle in aquaporin-1 null mice.
pubmed:affiliation
Laboratory of Kidney and Electrolyte Metabolism, National Institutes of Health, Bethesda, Maryland 20892, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't