Translational studies on mitochondrial function and hypoxia in complications of diabetes mellitus
Author: Xu, Cheng
Date: 2020-12-18
Location: Lecture hall Clarence Crafoord, A5:04, Eugeniavägen 3, Karolinska Universitetssjukhuset, Solna
Time: 09.00
Department: Inst för molekylär medicin och kirurgi / Dept of Molecular Medicine and Surgery
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Thesis (16.72Mb)
Abstract
Diabetes Mellitus (DM) is a major concern for societies and healthcare systems globally. DM-associated morbidity and mortality is mediated by diabetic complications. Hypoxia and oxidative stress have emerged as key players in the pathogenesis of various macro- and microvascular complications of DM. This work aimed to investigate different aspects of the relationship between hypoxia, regulation of hypoxia inducible factor-1 (HIF-1), mitochondrial function and the development of common DM complications from a translational perspective.
Paper I investigates the endogenous antioxidant Coenzyme Q10 in a Swedish cohort of DM patients. We explored the association between markers of oxidative stress and the prevalence of vascular complications of DM. Our results showed hyperlipidemia, hyperglycemia, and inflammation to be associated with markers of oxidative stress, which in turn was correlated to the prevalence of diabetes complications such as peripheral neuropathy. In Paper II, we investigated a novel epoxidated Tocotrienol derivative exhibiting antioxidative properties affecting mitochondrial function. Mono-epoxy-tocotrienol-alpha was seen to stimulate pro-wound healing processes such as fibroblast migration rates and endothelial tube formation in vitro. The compound was also shown to increase wound closure rates in diabetic mice. This paper demonstrated experimentally that modulating mitochondrial function can improve factors underlying deficient wound healing in DM. The association between hypoxia regulation, wound healing and cellular bioenergetics in DM was studied in Paper III. HypoxamiR-210 (miR-210) is induced by HIF-1 in response to hypoxia. We found that hyperglycaemia reduced hypoxia-dependent miR-210 induction. miR- 210 increased the rate of wound healing in diabetic mice. The same treatment reduced oxygen consumption rate and ROS production in wound tissue. We thus showed that the hypoxia associated dysregulation in wound healing can be reversed through miR-210-mediated improvement of cellular metabolism. Finally, Paper IV explored the relationship between HIF-1 repression by hyperglycemia and overproduction of ROS in DM. Using a translational approach employing cell cultures, mice and human subjects exposed to hypoxic conditions, we showed that HIF-1-deficient induction of ROS production is specific feature in DM. Reversing this process was shown to be a protective factor against diabetic nephropathy. Hence, reversing impaired HIF-1 function is a potential therapeutic target in the treatment of DM complications.
Paper I investigates the endogenous antioxidant Coenzyme Q10 in a Swedish cohort of DM patients. We explored the association between markers of oxidative stress and the prevalence of vascular complications of DM. Our results showed hyperlipidemia, hyperglycemia, and inflammation to be associated with markers of oxidative stress, which in turn was correlated to the prevalence of diabetes complications such as peripheral neuropathy. In Paper II, we investigated a novel epoxidated Tocotrienol derivative exhibiting antioxidative properties affecting mitochondrial function. Mono-epoxy-tocotrienol-alpha was seen to stimulate pro-wound healing processes such as fibroblast migration rates and endothelial tube formation in vitro. The compound was also shown to increase wound closure rates in diabetic mice. This paper demonstrated experimentally that modulating mitochondrial function can improve factors underlying deficient wound healing in DM. The association between hypoxia regulation, wound healing and cellular bioenergetics in DM was studied in Paper III. HypoxamiR-210 (miR-210) is induced by HIF-1 in response to hypoxia. We found that hyperglycaemia reduced hypoxia-dependent miR-210 induction. miR- 210 increased the rate of wound healing in diabetic mice. The same treatment reduced oxygen consumption rate and ROS production in wound tissue. We thus showed that the hypoxia associated dysregulation in wound healing can be reversed through miR-210-mediated improvement of cellular metabolism. Finally, Paper IV explored the relationship between HIF-1 repression by hyperglycemia and overproduction of ROS in DM. Using a translational approach employing cell cultures, mice and human subjects exposed to hypoxic conditions, we showed that HIF-1-deficient induction of ROS production is specific feature in DM. Reversing this process was shown to be a protective factor against diabetic nephropathy. Hence, reversing impaired HIF-1 function is a potential therapeutic target in the treatment of DM complications.
List of papers:
I. Elisabete Forsberg*, Cheng Xu*, Jacob Grünler, Johan Frostegård, Michael Tekle, Kerstin Brismar, Lars Kärvestedt. Coenzyme Q10 and oxidative stress, the association with peripheral sensory neuropathy and cardiovascular disease in type 2 diabetes mellitus. J Diabetes Compliations. Nov-Dec 2015;29(8):1152-8. *Shared first authorship.
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II. Cheng Xu, Magnus Bentinger, Octavian Savu, Ali Mosfegh, Vivekananda Sunkari, Gustav Dallner, Ewa Swiezewska, Sergiu-Bogdan Catrina, Kerstin Brismar, Michael Tekle. Mono-epoxy-tocotrienol-alpha enhances wound healing in diabetic mice and stimulates in vitro angiogenesis and cell migration. J Diabetes Complications. 2017 Jan;31(1):4-12.
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III. Sampath Narayanan, Sofie Eliasson, Cheng Xu, Jacob Grünler, Allan Zhao, Wan Zhu, Ning Xu Landén, Mona Ståhle, Jingping Zhang, Mircea Ivan, Raluca Georgiana Maltesen, Ileana Ruxandra Botusan, Neda Rajamand Ekberg, Xiaowei Zheng, Sergiu-Bogdan Catrina. HypoxamiR-210 accelerates wound healing in diabetes by improving cellular metabolism. Comms Bio. [Accepted]
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IV. Xiaowei Zheng*, Sampath Narayanan*, Cheng Xu*, Sofie Eliasson, Jacob Grünler, Allan Zhao, Alessandro di Torro, Luciano Bernardi, Massimiliano Massone, Peter Carmeliet, Marianna del Sole, Giancarlo Solaini, Kerstin Brismar, Tomas A. Schiffer, Ileana Ruxandra Botusan, Neda Rajamand Ekberg, Fredrik Palm, Sergiu-Bogdan Catrina. Repression of Hypoxia inducible Factor 1 (HIF-1) in diabetes contributes to the increase of mitochondrial radical oxygen species (ROS) production. *Shared first authorship. [Manuscript]
I. Elisabete Forsberg*, Cheng Xu*, Jacob Grünler, Johan Frostegård, Michael Tekle, Kerstin Brismar, Lars Kärvestedt. Coenzyme Q10 and oxidative stress, the association with peripheral sensory neuropathy and cardiovascular disease in type 2 diabetes mellitus. J Diabetes Compliations. Nov-Dec 2015;29(8):1152-8. *Shared first authorship.
Fulltext (DOI)
Pubmed
View record in Web of Science®
II. Cheng Xu, Magnus Bentinger, Octavian Savu, Ali Mosfegh, Vivekananda Sunkari, Gustav Dallner, Ewa Swiezewska, Sergiu-Bogdan Catrina, Kerstin Brismar, Michael Tekle. Mono-epoxy-tocotrienol-alpha enhances wound healing in diabetic mice and stimulates in vitro angiogenesis and cell migration. J Diabetes Complications. 2017 Jan;31(1):4-12.
Fulltext (DOI)
Pubmed
View record in Web of Science®
III. Sampath Narayanan, Sofie Eliasson, Cheng Xu, Jacob Grünler, Allan Zhao, Wan Zhu, Ning Xu Landén, Mona Ståhle, Jingping Zhang, Mircea Ivan, Raluca Georgiana Maltesen, Ileana Ruxandra Botusan, Neda Rajamand Ekberg, Xiaowei Zheng, Sergiu-Bogdan Catrina. HypoxamiR-210 accelerates wound healing in diabetes by improving cellular metabolism. Comms Bio. [Accepted]
Fulltext (DOI)
Pubmed
View record in Web of Science®
IV. Xiaowei Zheng*, Sampath Narayanan*, Cheng Xu*, Sofie Eliasson, Jacob Grünler, Allan Zhao, Alessandro di Torro, Luciano Bernardi, Massimiliano Massone, Peter Carmeliet, Marianna del Sole, Giancarlo Solaini, Kerstin Brismar, Tomas A. Schiffer, Ileana Ruxandra Botusan, Neda Rajamand Ekberg, Fredrik Palm, Sergiu-Bogdan Catrina. Repression of Hypoxia inducible Factor 1 (HIF-1) in diabetes contributes to the increase of mitochondrial radical oxygen species (ROS) production. *Shared first authorship. [Manuscript]
Institution: Karolinska Institutet
Supervisor: Catrina, Sergiu-Bogdan
Co-supervisor: Brismar, Kerstin; Zheng, Xiaowei; Tekle, Michael
Issue date: 2020-11-24
Rights:
Publication year: 2020
ISBN: 978-91-7831-989-3
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