Adiponectin accumulation in the retinal vascular endothelium and its possible role in preventing early diabetic microvascular damage.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
09 03 2022
Historique:
received: 04 11 2021
accepted: 28 02 2022
entrez: 10 3 2022
pubmed: 11 3 2022
medline: 27 4 2022
Statut: epublish

Résumé

Adiponectin (APN), a protein abundantly secreted from adipocytes, has been reported to possess beneficial effects on cardiovascular diseases in association with its accumulation on target organs and cells by binding to T-cadherin. However, little is known about the role of APN in the development of diabetic microvascular complications, such as diabetic retinopathy (DR). Here we investigated the impact of APN on the progression of early retinal vascular damage using a streptozotocin (STZ)-induced diabetic mouse model. Our immunofluorescence results clearly showed T-cadherin-dependent localization of APN in the vascular endothelium of retinal arterioles, which was progressively decreased during the course of diabetes. Such reduction of retinal APN accompanied the early features of DR, represented by increased vascular permeability, and was prevented by glucose-lowering therapy with dapagliflozin, a selective sodium-glucose co-transporter 2 inhibitor. In addition, APN deficiency resulted in severe vascular permeability under relatively short-term hyperglycemia, together with a significant increase in vascular cellular adhesion molecule-1 (VCAM-1) and a reduction in claudin-5 in the retinal endothelium. The present study demonstrated a possible protective role of APN against the development of DR.

Identifiants

pubmed: 35264685
doi: 10.1038/s41598-022-08041-2
pii: 10.1038/s41598-022-08041-2
pmc: PMC8907357
doi:

Substances chimiques

Adiponectin 0
Glucose IY9XDZ35W2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4159

Informations de copyright

© 2022. The Author(s).

Références

Maeda, N. et al. Diet-induced insulin resistance in mice lacking adiponectin/ACRP30. Nat. Med. 8, 731–737 (2002).
pubmed: 12068289 doi: 10.1038/nm724
Fujita, K. et al. Adiponectin protects against angiotensin II-induced cardiac fibrosis through activation of PPAR-alpha. Arterioscler. Thromb. Vasc. Biol. 28, 863–870 (2008).
pubmed: 18309113 doi: 10.1161/ATVBAHA.107.156687
Kamada, Y. et al. Enhanced carbon tetrachloride-induced liver fibrosis in mice lacking adiponectin. Gastroenterology 125, 1796–1807 (2003).
pubmed: 14724832 doi: 10.1053/j.gastro.2003.08.029
Shimano, M. et al. Adiponectin deficiency exacerbates cardiac dysfunction following pressure overload through disruption of an AMPK-dependent angiogenic response. J. Mol. Cell. Cardiol. 49, 210–220 (2010).
pubmed: 20206634 pmcid: 2885542 doi: 10.1016/j.yjmcc.2010.02.021
Okamoto, Y. et al. Adiponectin reduces atherosclerosis in apolipoprotein E-deficient mice. Circulation 106, 2767–2770 (2002).
pubmed: 12451000 doi: 10.1161/01.CIR.0000042707.50032.19
Kishida, K. et al. Relationships between circulating adiponectin levels and fat distribution in obese subjects. J. Atheroscler. Thromb. 18, 592–595 (2011).
pubmed: 21378472 doi: 10.5551/jat.7625
Hotta, K. et al. Plasma concentrations of a novel, adipose-specific protein, adiponectin, in type 2 diabetic patients. Arterioscler. Thromb. Vasc. Biol. 20, 1595–1599 (2000).
pubmed: 10845877 doi: 10.1161/01.ATV.20.6.1595
Fujishima, Y. et al. Adiponectin association with T-cadherin protects against neointima proliferation and atherosclerosis. FASEB. J. 31, 1571–1583 (2017).
pubmed: 28062540 doi: 10.1096/fj.201601064R
Denzel, M. S. et al. T-cadherin is critical for adiponectin-mediated cardioprotection in mice. J. Clin. Invest. 120, 4342–4352 (2010).
pubmed: 21041950 pmcid: 2993592 doi: 10.1172/JCI43464
Tanaka, Y. et al. Adiponectin promotes muscle regeneration through binding to T-cadherin. Sci. Rep. 9, 16 (2019).
pubmed: 30626897 pmcid: 6327035 doi: 10.1038/s41598-018-37115-3
Tsugawa-Shimizu, Y. et al. Increased vascular permeability and severe renal tubular damage after ischemia-reperfusion injury in mice lacking adiponectin or T-cadherin. Am. J. Physiol. Endocrinol. Metab. 320, E179-190 (2021).
pubmed: 33284092 doi: 10.1152/ajpendo.00393.2020
Ogurtsova, K. et al. IDF Diabetes Atlas: Global estimates for the prevalence of diabetes for 2015 and 2040. Diabetes. Res. Clin. Pract. 128, 40–50 (2017).
pubmed: 28437734 doi: 10.1016/j.diabres.2017.03.024
Antonetti, D. A., Silva, P. S. & Stitt, A. W. Current understanding of the molecular and cellular pathology of diabetic retinopathy. Nat. Rev. Endocrinol. 17, 195–206 (2021).
pubmed: 33469209 doi: 10.1038/s41574-020-00451-4
Sharma, K. et al. Adiponectin regulates albuminuria and podocyte function in mice. J. Clin. Invest. 118, 1645–1656 (2008).
pubmed: 18431508 pmcid: 2323186
Vinores, S. A., Gadegbeku, C., Campochiaro, P. A. & Green, W. R. Immunohistochemical localization of blood–retinal barrier breakdown in human diabetics. Am. J. Pathol. 134, 231–235 (1989).
pubmed: 2916645 pmcid: 1879597
Kim, Y. H., Kim, Y. S., Roh, G. S., Choi, W. S. & Cho, G. J. Resveratrol blocks diabetes-induced early vascular lesions and vascular endothelial growth factor induction in mouse retinas. Acta. Ophthalmol. 90, e31–e37 (2012).
pubmed: 21914146 doi: 10.1111/j.1755-3768.2011.02243.x
Bai, N., Tang, S., Ma, J., Luo, Y. & Lin, S. Increased expression of intercellular adhesion molecule-1, vascular cellular adhesion molecule-1 and leukocyte common antigen in diabetic rat retina. Yan Ke Xue Bao 19, 176–183 (2003).
pubmed: 14574977
Gustavsson, C. et al. Vascular cellular adhesion molecule-1 (VCAM-1) expression in mice retinal vessels is affected by both hyperglycemia and hyperlipidemia. PLoS ONE 5, e12699 (2010).
pubmed: 20856927 pmcid: 2938334 doi: 10.1371/journal.pone.0012699
Khalfaoui, T., Lizard, G. & Ouertani-Meddeb, A. Adhesion molecules (ICAM-1 and VCAM-1) and diabetic retinopathy in type 2 diabetes. J. Mol. Histol. 39, 243–249 (2008).
pubmed: 18165914 doi: 10.1007/s10735-007-9159-5
Díaz-Coránguez, M., Ramos, C. & Antonetti, D. A. The inner blood-retinal barrier: Cellular basis and development. Vision. Res. 139, 123–137 (2017).
pubmed: 28619516 pmcid: 5723228 doi: 10.1016/j.visres.2017.05.009
Kita, S., Fukuda, S., Maeda, N. & Shimomura, I. Native adiponectin in serum binds to mammalian cells expressing T-cadherin, but not AdipoRs or calreticulin. Elife 8, e48675 (2019).
pubmed: 31647413 pmcid: 6822988 doi: 10.7554/eLife.48675
Nakamura, Y. et al. Adiponectin stimulates exosome release to enhance mesenchymal stem-cell-driven therapy of heart failure in mice. Mol. Ther. 28, 2203–2219 (2020).
pubmed: 32652045 pmcid: 7351027 doi: 10.1016/j.ymthe.2020.06.026
Yousef, H. et al. Aged blood impairs hippocampal neural precursor activity and activates microglia via brain endothelial cell VCAM1. Nat. Med. 25, 988–1000 (2019).
pubmed: 31086348 pmcid: 6642642 doi: 10.1038/s41591-019-0440-4
Yilmaz, M. I. et al. Adiponectin may play a part in the pathogenesis of diabetic retinopathy. Eur. J. Endocrinol. 151, 135–140 (2004).
pubmed: 15248834 doi: 10.1530/eje.0.1510135
Yang, H. S. et al. Serum and aqueous humor adiponectin levels correlate with diabetic retinopathy development and progression. PLoS ONE 16, e0259683 (2021).
pubmed: 34780524 pmcid: 8592425 doi: 10.1371/journal.pone.0259683
Obata, Y. et al. Relationship between serum adiponectin levels and age in healthy subjects and patients with type 2 diabetes. Clin. Endocrinol. (Oxf) 79, 204–210 (2013).
doi: 10.1111/cen.12041
Matsuda, K. et al. Positive feedback regulation between adiponectin and T-cadherin impacts adiponectin levels in tissue and plasma of male mice. Endocrinology 156, 934–946 (2015).
pubmed: 25514086 doi: 10.1210/en.2014-1618
Fukuda, S. et al. The unique prodomain of T-cadherin plays a key role in adiponectin binding with the essential extracellular cadherin repeats 1 and 2. J. Biol. Chem. 292, 7840–7849 (2017).
pubmed: 28325833 pmcid: 5427265 doi: 10.1074/jbc.M117.780734
Vallon, V. & Thomson, S. C. The tubular hypothesis of nephron filtration and diabetic kidney disease. Nat. Rev. Nephrol. 16, 317–336 (2020).
pubmed: 32152499 pmcid: 7242158 doi: 10.1038/s41581-020-0256-y
Mancini, S. J. et al. Canagliflozin inhibits interleukin-1β-stimulated cytokine and chemokine secretion in vascular endothelial cells by AMP-activated protein kinase-dependent and -independent mechanisms. Sci. Rep. 8, 5276 (2018).
pubmed: 29588466 pmcid: 5869674 doi: 10.1038/s41598-018-23420-4
Wakisaka, M. & Nagao, T. Sodium glucose cotransporter 2 in mesangial cells and retinal pericytes and its implications for diabetic nephropathy and retinopathy. Glycobiology 27, 691–695 (2017).
pubmed: 28535208 pmcid: 5881757 doi: 10.1093/glycob/cwx047
Mudaliar, S., Hupfeld, C. & Chao, D. L. SGLT2 inhibitor-induced low-grade ketonemia ameliorates retinal hypoxia in diabetic retinopathy-a novel hypothesis. J. Clin. Endocrinol. Metab. 106, 1235–1244 (2021).
pubmed: 33512450 doi: 10.1210/clinem/dgab050
Omae, T., Nagaoka, T. & Yoshida, A. Relationship between retinal blood flow and serum adiponectin concentrations in patients with type 2 diabetes mellitus. Invest. Ophthalmol. Vis. Sci. 56, 4143–4149 (2015).
pubmed: 26114492 doi: 10.1167/iovs.15-16447
Omae, T., Nagaoka, T., Tanano, I. & Yoshida, A. Adiponectin-induced dilation of isolated porcine retinal arterioles via production of nitric oxide from endothelial cells. Invest. Ophthalmol. Vis. Sci. 54, 4586–4594 (2013).
pubmed: 23737475 doi: 10.1167/iovs.13-11756
Higuchi, A., Ohashi, K., Kihara, S., Walsh, K. & Ouchi, N. Adiponectin suppresses pathological microvessel formation in retina through modulation of tumor necrosis factor-alpha expression. Circ. Res. 104, 1058–1065 (2009).
pubmed: 19342600 pmcid: 2740643 doi: 10.1161/CIRCRESAHA.109.194506
Forrester, J. V., Kuffova, L. & Delibegovic, M. The role of inflammation in diabetic retinopathy. Front. Immunol. 11, 583687 (2020).
pubmed: 33240272 pmcid: 7677305 doi: 10.3389/fimmu.2020.583687
Ouchi, N. et al. Adiponectin, an adipocyte-derived plasma protein, inhibits endothelial NF-kappaB signaling through a cAMP-dependent pathway. Circulation 102, 1296–1301 (2000).
pubmed: 10982546 doi: 10.1161/01.CIR.102.11.1296
Mandal, N. et al. Role of ceramides in the pathogenesis of diabetes mellitus and its complications. J. Diabetes. Complications. 35, 107734 (2021).
pubmed: 33268241 doi: 10.1016/j.jdiacomp.2020.107734
Obata, Y. et al. Adiponectin/T-cadherin system enhances exosome biogenesis and decreases cellular ceramides by exosomal release. JCI Insight 3, e99680 (2018).
pmcid: 5931116 doi: 10.1172/jci.insight.99680
Arima, M. et al. Claudin-5 redistribution induced by inflammation leads to anti-VEGF-resistant diabetic macular edema. Diabetes 69, 981–999 (2020).
pubmed: 32139595 doi: 10.2337/db19-1121
Arima, M. et al. Basigin can be a therapeutic target to restore the retinal vascular barrier function in the mouse model of diabetic retinopathy. Sci. Rep. 6, 38445 (2016).
pubmed: 27917946 pmcid: 5137162 doi: 10.1038/srep38445
Aveleira, C. A., Lin, C. M., Abcouwer, S. F., Ambrósio, A. F. & Antonetti, D. A. TNF-α signals through PKCζ/NF-κB to alter the tight junction complex and increase retinal endothelial cell permeability. Diabetes 59, 2872–2882 (2010).
pubmed: 20693346 pmcid: 2963546 doi: 10.2337/db09-1606
Nitta, T. et al. Size-selective loosening of the blood-brain barrier in claudin-5-deficient mice. J. Cell. Biol. 161, 653–660 (2003).
pubmed: 12743111 pmcid: 2172943 doi: 10.1083/jcb.200302070
Lv, J. et al. Focusing on claudin-5: A promising candidate in the regulation of BBB to treat ischemic stroke. Prog. Neurobiol. 161, 79–96 (2018).
pubmed: 29217457 doi: 10.1016/j.pneurobio.2017.12.001
Thrailkill, K. M. et al. Matrix metalloproteinase-2 dysregulation in type 1 diabetes. Diabetes Care 30, 2321–2326 (2007).
pubmed: 17563344 doi: 10.2337/dc07-0162
Jacqueminet, S. et al. Elevated circulating levels of matrix metalloproteinase-9 in type 1 diabetic patients with and without retinopathy. Clin. Chim. Acta. 367, 103–107 (2006).
pubmed: 16426593 doi: 10.1016/j.cca.2005.11.029
Liu, J., Jin, X., Liu, K. J. & Liu, W. Matrix metalloproteinase-2-mediated occludin degradation and caveolin-1-mediated claudin-5 redistribution contribute to blood-brain barrier damage in early ischemic stroke stage. J. Neurosci. 2012(32), 3044–3057 (2012).
doi: 10.1523/JNEUROSCI.6409-11.2012
Chiu, P. S. & Lai, S. C. Matrix metalloproteinase-9 leads to claudin-5 degradation via the NF-κB pathway in BALB/c mice with eosinophilic meningoencephalitis caused by Angiostrongylus cantonensis. PLoS ONE 8, e53370 (2013).
pubmed: 23505411 pmcid: 3591436 doi: 10.1371/journal.pone.0053370
Stamatovic, S. M., Keep, R. F., Wang, M. M., Jankovic, I. & Andjelkovic, A. V. Caveolae-mediated internalization of occludin and claudin-5 during CCL2-induced tight junction remodeling in brain endothelial cells. J. Biol. Chem. 284, 19053–19066 (2009).
pubmed: 19423710 pmcid: 2707189 doi: 10.1074/jbc.M109.000521
Miksztowicz, V. et al. Adiponectin predicts MMP-2 activity independently of obesity. Eur. J. Clin. Invest. 44, 951–957 (2014).
pubmed: 25145771 doi: 10.1111/eci.12328
Cheng, M., Hashmi, S., Mao, X. & Zeng, Q. T. Relationships of adiponectin and matrix metalloproteinase-9 to tissue inhibitor of metalloproteinase-1 ratio with coronary plaque morphology in patients with acute coronary syndrome. Can. J. Cardiol. 24, 385–390 (2008).
pubmed: 18464944 pmcid: 2643141 doi: 10.1016/S0828-282X(08)70602-0
Essick, E. E. et al. Adiponectin mediates cardioprotection in oxidative stress-induced cardiac myocyte remodeling. Am. J. Physiol. Heart. Circ. Physiol. 301, H984-993 (2011).
pubmed: 21666115 pmcid: 3191107 doi: 10.1152/ajpheart.00428.2011
Nishinaka, A. et al. Excess adiponectin in eyes with progressive ocular vascular diseases. FASEB. J. 35, e21313 (2021).
pubmed: 33484194 doi: 10.1096/fj.202001740RR
Hebbard, L. W. et al. T-cadherin supports angiogenesis and adiponectin association with the vasculature in a mouse mammary tumor model. Can. Res. 68, 1407–1416 (2008).
doi: 10.1158/0008-5472.CAN-07-2953
Nishitani, S. et al. Metabolomic and microarray analyses of adipose tissue of dapagliflozin-treated mice, and effects of 3-hydroxybutyrate on induction of adiponectin in adipocytes. Sci. Rep. 8, 8805 (2018).
pubmed: 29891844 pmcid: 5995811 doi: 10.1038/s41598-018-27181-y
Fukushima, Y. et al. Sema3E-PlexinD1 signaling selectively suppresses disoriented angiogenesis in ischemic retinopathy in mice. J. Clin. Invest. 121, 1974–1985 (2011).
pubmed: 21505259 pmcid: 3083763 doi: 10.1172/JCI44900

Auteurs

Taka-Aki Sakaue (TA)

Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, 2-2-B5, Yamada-oka, Suita, Osaka, 565-0871, Japan.

Yuya Fujishima (Y)

Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, 2-2-B5, Yamada-oka, Suita, Osaka, 565-0871, Japan. y.fujishima@endmet.med.osaka-u.ac.jp.

Yoko Fukushima (Y)

Department of Ophthalmology, Graduate School of Medicine, Osaka University, 2-2-B5, Yamada-oka, Suita, Osaka, 565-0871, Japan.
Integrated Frontier Research for Medical Science Division, Institute for Open and Transdisciplinary Research Initiatives, Osaka University, 2-2, Yamada-oka, Suita, Osaka, 565-0871, Japan.

Yuri Tsugawa-Shimizu (Y)

Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, 2-2-B5, Yamada-oka, Suita, Osaka, 565-0871, Japan.

Shiro Fukuda (S)

Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, 2-2-B5, Yamada-oka, Suita, Osaka, 565-0871, Japan.

Shunbun Kita (S)

Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, 2-2-B5, Yamada-oka, Suita, Osaka, 565-0871, Japan.
Department of Adipose Management, Graduate School of Medicine, Osaka University, 2-2, Yamada-oka, Suita, Osaka, Japan.

Hitoshi Nishizawa (H)

Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, 2-2-B5, Yamada-oka, Suita, Osaka, 565-0871, Japan.

Barbara Ranscht (B)

Sanford Burnham Prebys Medical Discovery Institute, NIH-Designated Cancer Center, Development, Aging and Regeneration Program, La Jolla, CA, USA.

Kohji Nishida (K)

Department of Ophthalmology, Graduate School of Medicine, Osaka University, 2-2-B5, Yamada-oka, Suita, Osaka, 565-0871, Japan.
Integrated Frontier Research for Medical Science Division, Institute for Open and Transdisciplinary Research Initiatives, Osaka University, 2-2, Yamada-oka, Suita, Osaka, 565-0871, Japan.

Norikazu Maeda (N)

Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, 2-2-B5, Yamada-oka, Suita, Osaka, 565-0871, Japan.
Department of Metabolism and Atherosclerosis, Graduate School of Medicine Osaka University, 2-2, Yamada-oka, Suita, Osaka, 565-0871, Japan.

Iichiro Shimomura (I)

Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, 2-2-B5, Yamada-oka, Suita, Osaka, 565-0871, Japan.

Articles similaires

Robotic Surgical Procedures Animals Humans Telemedicine Models, Animal

Odour generalisation and detection dog training.

Lyn Caldicott, Thomas W Pike, Helen E Zulch et al.
1.00
Animals Odorants Dogs Generalization, Psychological Smell
Animals TOR Serine-Threonine Kinases Colorectal Neoplasms Colitis Mice
Animals Tail Swine Behavior, Animal Animal Husbandry

Classifications MeSH