Angiotensin II-Independent Upregulation of Cyclooxygenase-2 by Activation of the (Pro) Renin Receptor in Rat Renal Inner Medullary Cells
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作者:
Gonzalez, Alexis A.
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Tulane Univ, Sch Med, Renal & Hypertens Ctr Excellence, New Orleans, LA 70112 USATulane Univ, Hlth Sci Ctr, Dept Physiol, Sch Med, New Orleans, LA 70112 USA
Gonzalez, Alexis A.
[2
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Luffman, Christina
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机构:Tulane Univ, Hlth Sci Ctr, Dept Physiol, Sch Med, New Orleans, LA 70112 USA
Luffman, Christina
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Bourgeois, Camille R. T.
Vio, Carlos P.
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Pontificia Univ Catolica Chile, Santiago, ChileTulane Univ, Hlth Sci Ctr, Dept Physiol, Sch Med, New Orleans, LA 70112 USA
Vio, Carlos P.
[3
]
Prieto, Minolfa C.
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Tulane Univ, Hlth Sci Ctr, Dept Physiol, Sch Med, New Orleans, LA 70112 USA
Tulane Univ, Sch Med, Renal & Hypertens Ctr Excellence, New Orleans, LA 70112 USA
Tulane Univ, Tulane BIRCWH Program, New Orleans, LA 70112 USATulane Univ, Hlth Sci Ctr, Dept Physiol, Sch Med, New Orleans, LA 70112 USA
Prieto, Minolfa C.
[1
,2
,4
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机构:
[1] Tulane Univ, Hlth Sci Ctr, Dept Physiol, Sch Med, New Orleans, LA 70112 USA
[2] Tulane Univ, Sch Med, Renal & Hypertens Ctr Excellence, New Orleans, LA 70112 USA
During renin-angiotensin system activation, cyclooxygenase-2 (COX-2)-derived prostaglandins attenuate the pressor and antinatriuretic effects of angiotensin II (AngII) in the renal medulla. The (pro)renin receptor (PRR) is abundantly expressed in the collecting ducts (CD) and its expression is augmented by AngII. PRR overexpression upregulates COX-2 via mitogen-activated kinases/extracellular regulated kinases 1/2 in renal tissues; however, it is not clear whether this effect occurs independently or in concert with AngII type 1 receptor (AT(1)R) activation. We hypothesized that PRR activation stimulates COX-2 expression independently of AT(1)R in primary cultures of rat renal inner medullary cells. The use of different cell-specific immunomarkers (aquaporin-2 for principal cells, anion exchanger type 1 for intercalated type-A cells, and tenascin C for interstitial cells) and costaining for AT(1)R, COX-2, and PRR revealed that PRR and COX-2 were colocalized in intercalated and interstitial cells whereas principal cells did not express PRR or COX-2. In normal rat kidney sections, PRR and COX-2 were colocalized in intercalated and interstitial cells. In rat renal inner medullary cultured cells, treatment with AngII (100 nmol/L) increased COX-2 expression via AT(1)R. In addition, AngII and rat recombinant prorenin (100 nmol/L) treatments increased extracellular regulated kinases 1/2 phosphorylation, independently. Importantly, rat recombinant prorenin upregulated COX-2 expression in the presence of AT(1)R blockade. Inhibition of mitogen-activated kinases/extracellular regulated kinases 1/2 suppressed COX-2 upregulation mediated by either AngII or rat recombinant prorenin. Furthermore, PRR knockdown using PRR-short hairpin RNA blunted the rat recombinant prorenin-mediated upregulation of COX-2. These results indicate that COX-2 expression is upregulated by activation of either PRR or AT(1)R via mitogen-activated kinases/extracellular regulated kinases 1/2 in rat renal inner medullary cells. (Hypertension. 2013;61:443-449.) circle Online Data Supplement
机构:
Dalian Med Univ, Dalian 116021, Liaoning Provin, Peoples R ChinaDalian Med Univ, Dalian 116021, Liaoning Provin, Peoples R China
Liu, Feng Y.
Liu, Xiao Y.
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Dalian Med Univ, Dalian 116021, Liaoning Provin, Peoples R ChinaDalian Med Univ, Dalian 116021, Liaoning Provin, Peoples R China
Liu, Xiao Y.
Zhang, Li J.
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Dalian Med Univ, Dalian 116021, Liaoning Provin, Peoples R ChinaDalian Med Univ, Dalian 116021, Liaoning Provin, Peoples R China
Zhang, Li J.
Cheng, Yun P.
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Dalian Med Univ, Affiliated Hosp 1, Dept Cardiol, Dalian 116021, Liaoning Provin, Peoples R ChinaDalian Med Univ, Dalian 116021, Liaoning Provin, Peoples R China
Cheng, Yun P.
Jiang, Yi N.
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Dalian Med Univ, Affiliated Hosp 1, Dept Cardiol, Dalian 116021, Liaoning Provin, Peoples R ChinaDalian Med Univ, Dalian 116021, Liaoning Provin, Peoples R China
机构:
Yonsei Univ, Coll Human Ecol, Brain Korea PLUS Project 21, Dept Food & Nutr, Seoul 03722, South KoreaYonsei Univ, Coll Human Ecol, Brain Korea PLUS Project 21, Dept Food & Nutr, Seoul 03722, South Korea
Han, Hwana
Lim, Joo Weon
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Yonsei Univ, Coll Human Ecol, Brain Korea PLUS Project 21, Dept Food & Nutr, Seoul 03722, South KoreaYonsei Univ, Coll Human Ecol, Brain Korea PLUS Project 21, Dept Food & Nutr, Seoul 03722, South Korea
机构:
Tsuchiura Kyodo Gen Hosp, Dept Urol, Tsuchiura, Ibaraki, JapanTokyo Med & Dent Univ, Dept Urol, Bunkyo Ku, Tokyo 1138519, Japan
Tatokoro, Manabu
Fujii, Yasuhisa
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Tokyo Med & Dent Univ, Dept Urol, Bunkyo Ku, Tokyo 1138519, Japan
Japanese Fdn Canc Res, Canc Inst Hosp, Dept Urol, Tokyo, JapanTokyo Med & Dent Univ, Dept Urol, Bunkyo Ku, Tokyo 1138519, Japan
Fujii, Yasuhisa
Kawakami, Satoru
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Japanese Fdn Canc Res, Canc Inst Hosp, Dept Urol, Tokyo, JapanTokyo Med & Dent Univ, Dept Urol, Bunkyo Ku, Tokyo 1138519, Japan
Kawakami, Satoru
Fukui, Naotaka
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Tsuchiura Kyodo Gen Hosp, Dept Urol, Tsuchiura, Ibaraki, JapanTokyo Med & Dent Univ, Dept Urol, Bunkyo Ku, Tokyo 1138519, Japan
Fukui, Naotaka
Komai, Yoshinobu
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Japanese Fdn Canc Res, Canc Inst Hosp, Dept Urol, Tokyo, JapanTokyo Med & Dent Univ, Dept Urol, Bunkyo Ku, Tokyo 1138519, Japan
Komai, Yoshinobu
Saito, Kazutaka
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Tsuchiura Kyodo Gen Hosp, Dept Urol, Tsuchiura, Ibaraki, JapanTokyo Med & Dent Univ, Dept Urol, Bunkyo Ku, Tokyo 1138519, Japan
Saito, Kazutaka
Koga, Fumitaka
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机构:Tokyo Med & Dent Univ, Dept Urol, Bunkyo Ku, Tokyo 1138519, Japan
Koga, Fumitaka
Morimoto, Shinji
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Tsuchiura Kyodo Gen Hosp, Dept Urol, Tsuchiura, Ibaraki, JapanTokyo Med & Dent Univ, Dept Urol, Bunkyo Ku, Tokyo 1138519, Japan
Morimoto, Shinji
Fukui, Iwao
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Japanese Fdn Canc Res, Canc Inst Hosp, Dept Urol, Tokyo, JapanTokyo Med & Dent Univ, Dept Urol, Bunkyo Ku, Tokyo 1138519, Japan
Fukui, Iwao
Kihara, Kazunori
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机构:Tokyo Med & Dent Univ, Dept Urol, Bunkyo Ku, Tokyo 1138519, Japan