Characterization of aquaporin 4 protein expression and localization in tissues of the dogfish (Squalus acanthias).

The role of aquaporin water channels in Elasmobanchs such as the dogfish Squalus acanthias is completely unknown. This investigation determines the expression and cellular and sub-cellular localization of AQP4 protein in dogfish tissues. Two polyclonal antibodies were generated (AQP4/1 and AQP4/2)....

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Main Authors: Christopher P Cutler, Sheena eHarmon, Jonathon eWalsh, Kia eBurch
Format: Article
Language:English
Published: Frontiers Media S.A. 2012-02-01
Series:Frontiers in Physiology
Subjects:
Na
Online Access:http://journal.frontiersin.org/Journal/10.3389/fphys.2012.00021/full
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spelling doaj-07e675630def4f498a1526e6de42e75d2020-11-24T20:40:14ZengFrontiers Media S.A.Frontiers in Physiology1664-042X2012-02-01310.3389/fphys.2012.0002115388Characterization of aquaporin 4 protein expression and localization in tissues of the dogfish (Squalus acanthias).Christopher P Cutler0Christopher P Cutler1Sheena eHarmon2Sheena eHarmon3Jonathon eWalsh4Jonathon eWalsh5Kia eBurch6Kia eBurch7Georgia Southern UniversityMount Desert Island Biological LaboratoryGeorgia Southern UniversityMount Desert Island Biological LaboratoryGeorgia Southern UniversityMount Desert Island Biological LaboratoryGeorgia Southern UniversityMount Desert Island Biological LaboratoryThe role of aquaporin water channels in Elasmobanchs such as the dogfish Squalus acanthias is completely unknown. This investigation determines the expression and cellular and sub-cellular localization of AQP4 protein in dogfish tissues. Two polyclonal antibodies were generated (AQP4/1 and AQP4/2). Western blots using the AQP4/1 antibody showed two bands (35.5kDa and 49.5kDa) in most tissues similar to mammals. Liver and rectal gland showed further bands. However, unlike in mammals, AQP4 protein was expressed in all tissues including respiratory tract and liver. The AQP4/2 antibody appeared much less specific in blots. Both antibodies were used in immunohistochemistry and showed similar cellular localizations, although the AQP4/2 antibody had a more restricted sub-cellular distribution compared to AQP4/1 and therefore appeared to be more specific. In kidney a sub-set of tubules were stained which may represent intermediate tubule segments. AQP4/1 and AQP4/2 antibodies localized to the same tubules segments in serial sections although the intensity and sub-cellular distribution were different. AQP4/2 showed a basal or basolateral membrane distribution whereas AQP4/1 was often distributed throughout the cell including the nucleus. In rectal gland and cardiac stomach AQP4 was localized to secretary tubules but again AQP/1 and AQP/2 showed different sub-cellular distributions. In gill, both antibodies stained large cells in the primary filament and secondary lamellae. Again AQP4/1 antibody stained most or all the cell including the nucleus, whereas AQP4/2 had a plasma membrane and sometimes cytoplasmic distribution. Two types of large mitochondria-rich cells are known to exist in elasmobranches, that express either Na,K ATPase or V-type ATPase. Using Na,K-ATPase and V-type ATPase antibodies, AQP4 was colocalized with these proteins using the AQP4/1 antibody. Results show AQP4 is expressed in both (and all) branchial Na,K ATPase and V-type ATPase expressing cells.http://journal.frontiersin.org/Journal/10.3389/fphys.2012.00021/fullAquaporin 4DogfishKidneygillK-ATPaseNa
collection DOAJ
language English
format Article
sources DOAJ
author Christopher P Cutler
Christopher P Cutler
Sheena eHarmon
Sheena eHarmon
Jonathon eWalsh
Jonathon eWalsh
Kia eBurch
Kia eBurch
spellingShingle Christopher P Cutler
Christopher P Cutler
Sheena eHarmon
Sheena eHarmon
Jonathon eWalsh
Jonathon eWalsh
Kia eBurch
Kia eBurch
Characterization of aquaporin 4 protein expression and localization in tissues of the dogfish (Squalus acanthias).
Frontiers in Physiology
Aquaporin 4
Dogfish
Kidney
gill
K-ATPase
Na
author_facet Christopher P Cutler
Christopher P Cutler
Sheena eHarmon
Sheena eHarmon
Jonathon eWalsh
Jonathon eWalsh
Kia eBurch
Kia eBurch
author_sort Christopher P Cutler
title Characterization of aquaporin 4 protein expression and localization in tissues of the dogfish (Squalus acanthias).
title_short Characterization of aquaporin 4 protein expression and localization in tissues of the dogfish (Squalus acanthias).
title_full Characterization of aquaporin 4 protein expression and localization in tissues of the dogfish (Squalus acanthias).
title_fullStr Characterization of aquaporin 4 protein expression and localization in tissues of the dogfish (Squalus acanthias).
title_full_unstemmed Characterization of aquaporin 4 protein expression and localization in tissues of the dogfish (Squalus acanthias).
title_sort characterization of aquaporin 4 protein expression and localization in tissues of the dogfish (squalus acanthias).
publisher Frontiers Media S.A.
series Frontiers in Physiology
issn 1664-042X
publishDate 2012-02-01
description The role of aquaporin water channels in Elasmobanchs such as the dogfish Squalus acanthias is completely unknown. This investigation determines the expression and cellular and sub-cellular localization of AQP4 protein in dogfish tissues. Two polyclonal antibodies were generated (AQP4/1 and AQP4/2). Western blots using the AQP4/1 antibody showed two bands (35.5kDa and 49.5kDa) in most tissues similar to mammals. Liver and rectal gland showed further bands. However, unlike in mammals, AQP4 protein was expressed in all tissues including respiratory tract and liver. The AQP4/2 antibody appeared much less specific in blots. Both antibodies were used in immunohistochemistry and showed similar cellular localizations, although the AQP4/2 antibody had a more restricted sub-cellular distribution compared to AQP4/1 and therefore appeared to be more specific. In kidney a sub-set of tubules were stained which may represent intermediate tubule segments. AQP4/1 and AQP4/2 antibodies localized to the same tubules segments in serial sections although the intensity and sub-cellular distribution were different. AQP4/2 showed a basal or basolateral membrane distribution whereas AQP4/1 was often distributed throughout the cell including the nucleus. In rectal gland and cardiac stomach AQP4 was localized to secretary tubules but again AQP/1 and AQP/2 showed different sub-cellular distributions. In gill, both antibodies stained large cells in the primary filament and secondary lamellae. Again AQP4/1 antibody stained most or all the cell including the nucleus, whereas AQP4/2 had a plasma membrane and sometimes cytoplasmic distribution. Two types of large mitochondria-rich cells are known to exist in elasmobranches, that express either Na,K ATPase or V-type ATPase. Using Na,K-ATPase and V-type ATPase antibodies, AQP4 was colocalized with these proteins using the AQP4/1 antibody. Results show AQP4 is expressed in both (and all) branchial Na,K ATPase and V-type ATPase expressing cells.
topic Aquaporin 4
Dogfish
Kidney
gill
K-ATPase
Na
url http://journal.frontiersin.org/Journal/10.3389/fphys.2012.00021/full
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