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Impact of The Protective Renin-Angiotensin System (RAS) on The Vasoreparative Function of CD34+ CACs in Diabetic RetinopathyPurpose: In diabetes, the impaired vasoreparative function of Circulating Angiogenic Cells (CACs) is believed to contribute to the progression of diabetic retinopathy (DR). Accumulating evidence suggests that the protective arm of renin-angiotensin system (RAS) ACE2 Angiotensin-(1-7) Mas plays an important role in restoring the function of diabetic CACs. We examined the protective RAS in CACs in diabetic individuals with different stages of retinopathy. Methods: Study subjects (n43) were recruited as controls or diabetics with either no DR, mild non-proliferative DR (NPDR), moderate NPDR, severe NPDR or proliferative DR (PDR). Fundus photography and fluorescein angiograms were analyzed using Vessel Generation Analysis (VESGEN) software in a cohort of subjects. CD34+ CACs were isolated from peripheral blood of diabetics and control subjects. RAS gene expressions in CACs were measured by qPCR. The vasoreparative function of CACs was assessed by migration ability toward CXCL12 using the QCM 5M 96-well chemotaxis cell migration assay. Results: ACE2 gene is a key enzyme converting the deleterious Angiotensin II to the beneficial Angiotensin-(1-7). ACE2 expression in CACs from diabetic subjects without DR was increased compared to controls, suggestive of compensation (p0.0437). The expression of Mas (Angiotensin-(1-7) receptor) in CACs was also increased in diabetics without DR, while was reduced in NPDR compared to controls (p0.0002), indicating a possible loss of compensation of the protective RAS at this stage of DR. The presence of even mild NPDR was associated with CD34+ CAC migratory dysfunction. When pretreating CACs of DR subjects with Angiotensin-(1-7), migratory ability to a chemoattractant CXCL12 was restored (p0.0008). By VESGEN analysis, an increase in small vessel density was observed in NPDR subjects when compared with the controls. Conclusions: These data suggest the protective RAS axis within diabetic CACs may help maintain their vasoreparative potential. The VESGEN analysis supports the presence of retinal repair in small vessels. The loss of the protective arm of RAS may predict the progression of DR.
Document ID
20160006388
Acquisition Source
Ames Research Center
Document Type
Presentation
Authors
Duan, Yaqian
(Indiana Univ. Indianapolis, IN, United States)
Moldovan, Leni
(Indiana Univ. Indianapolis, IN, United States)
Miller, Rehae C.
(Indiana Univ. Indianapolis, IN, United States)
Beli, Eleni
(Indiana Univ. Indianapolis, IN, United States)
Salazar, Tatiana
(Indiana Univ. Indianapolis, IN, United States)
Hazra, Sugata
(Utah Univ. Salt Lake City, UT, United States)
Al-Sabah, Jude
(Indiana Univ. Indianapolis, IN, United States)
Chalam, KV
(University of Florida Jacksonville, FL, United States)
Raghunandan, Sneha
(SGT, Inc. Moffett Field, CA, United States)
Vyas, Ruchi
(SGT, Inc. Moffett Field, CA, United States)
Parsons-Wingerter, Patricia
(NASA Ames Research Center Moffett Field, CA United States)
Oudit, Gavin Y.
(Alberta Univ. Calgary, Alberta, Canada)
Grant, Maria B.
(Indiana Univ. Indianapolis, IN, United States)
Date Acquired
May 18, 2016
Publication Date
May 1, 2016
Subject Category
Life Sciences (General)
Report/Patent Number
ARC-E-DAA-TN31942
Meeting Information
Meeting: ARVO 2016 Annual Meeting
Location: Seattle, WA
Country: United States
Start Date: May 1, 2016
End Date: May 5, 2016
Sponsors: Association for Research in Vision and Ophthalmology
Funding Number(s)
CONTRACT_GRANT: NNA14AA60C
Distribution Limits
Public
Copyright
Public Use Permitted.
Keywords
diabetes
retina
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