HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Enhanced erythropoiesis mediated by activation of the renin-angiotensin system via angiotensin II type 1a receptor.

Abstract
Although clinical and experimental studies have long suggested a role for the renin-angiotensin system (RAS) in the regulation of erythropoiesis, the molecular basis of this role has not been well understood. We report here that transgenic mice carrying both the human renin and human angiotensinogen genes displayed persistent erythrocytosis as well as hypertension. To identify the receptor molecule responsible for this phenotype, we introduced both transgenes into the AT1a receptor null background and found that the hematocrit level in the compound mice was restored to the normal level. Angiotensin II has been shown to influence erythropoiesis by two means, up-regulation of erythropoietin levels and direct stimulation of erythroid progenitor cells. Thus, we conducted bone marrow transplantation experiments and clarified that AT1a receptors on bone marrow-derived cells were dispensable for RAS-dependent erythrocytosis. Plasma erythropoietin levels and kidney erythropoietin mRNA expression in the double transgenic mice were significantly increased compared with those of the wild-type control, while the elevated plasma erythropoietin levels were significantly attenuated in the compound mice. These results provide clear genetic evidence that activated RAS enhances erythropoiesis through the AT1a receptor of kidney cells and that this effect is mediated by the elevation of plasma erythropoietin levels in vivo.
AuthorsHideki Kato, Junji Ishida, Shigehiko Imagawa, Tomoko Saito, Norio Suzuki, Toshiki Matsuoka, Takeshi Sugaya, Keiji Tanimoto, Takashi Yokoo, Osamu Ohneda, Fumihiro Sugiyama, Ken-ichi Yagami, Toshiro Fujita, Masayuki Yamamoto, Masaomi Nangaku, Akiyoshi Fukamizu
JournalFASEB journal : official publication of the Federation of American Societies for Experimental Biology (FASEB J) Vol. 19 Issue 14 Pg. 2023-5 (Dec 2005) ISSN: 1530-6860 [Electronic] United States
PMID16223784 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Angiotensins
  • RNA, Messenger
  • Receptor, Angiotensin, Type 1
  • Receptors, Angiotensin
  • Erythropoietin
  • Angiotensin II
  • Renin
Topics
  • Angiotensin II (metabolism)
  • Angiotensins (chemistry, genetics)
  • Animals
  • Bone Marrow Cells (cytology)
  • Bone Marrow Transplantation
  • Erythrocytes (cytology, metabolism)
  • Erythropoiesis
  • Erythropoietin (blood)
  • Hematocrit
  • Humans
  • Kidney (metabolism)
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Models, Biological
  • Phenotype
  • RNA, Messenger (metabolism)
  • Receptor, Angiotensin, Type 1 (chemistry, physiology)
  • Receptors, Angiotensin (chemistry)
  • Renin (chemistry, genetics)
  • Renin-Angiotensin System
  • Stem Cells
  • Transgenes
  • Up-Regulation

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: