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ADIPOR1 deficiency-induced suppression of retinal ELOVL2 and docosahexaenoic acid levels during photoreceptor degeneration and visual loss (本文)

長田, 秀斗 慶應義塾大学

2021.12.13

概要

Lipid metabolism-related gene mutations can cause retinitis pigmentosa, a currently untreatable blinding disease resulting from progressive neurodegeneration of the retina. Here, we demonstrated the influence of adiponectin receptor 1 (ADIPOR1) deficiency in retinal neurodegeneration using Adipor1 knockout (KO) mice. Adipor1 mRNA was observed to be expressed in photoreceptors, predominately within the photoreceptor inner segment (PIS), and increased after birth during the development of the photoreceptor outer segments (POSs) where photons are received by the visual pigment, rhodopsin. At 3 weeks of age, visual function impairment, specifically photoreceptor dysfunction, as recorded by electroretinography (ERG), was evident in homozygous, but not heterozygous, Adipor1 KO mice. However, although photoreceptor loss was evident at 3 weeks of age and progressed until 10 weeks, the level of visual dysfunction was already substantial by 3 weeks, after which it was retained until 10 weeks of age. The rhodopsin mRNA levels had already decreased at 3 weeks, suggesting that reduced rhodopsin may have contributed to early visual loss. Moreover, inflammation and oxidative stress were induced in homozygous KO retinas. Prior to observation of photoreceptor loss via optical microscopy, electron microscopy revealed that POSs were present; however, they were misaligned and their lipid composition, including docosahexaenoic acid (DHA), which is critical in forming POSs, was impaired in the retina. Importantly, the expression of Elovl2, an elongase of very long chain fatty acids expressed in the PIS, was significantly reduced, and lipogenic genes, which are induced under conditions of reduced endogenous DHA synthesis, were increased in homozygous KO mice. The causal relationship between ADIPOR1 deficiency and Elovl2 repression, together with upregulation of lipogenic genes, was confirmed in vitro. Therefore, ADIPOR1 in the retina appears to be indispensable for ELOVL2 induction, which is likely required to supply sufficient DHA for appropriate photoreceptor function and survival.

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参考文献

1. Engin, A. Adiponectin-Resistance in Obesity. Adv. Exp. Med. Biol. 960, 415–441 (2017).

2. Shamim, A., Mahmood, T., Ahsan, F., Kumar, A. & Bagga, P. Lipids: an insight into the neurodegenerative disorders. Clin. Nutr. Exp. 20, 1–19 (2018).

3. Sene, A. et al. Impaired cholesterol efflux in senescent macrophages promotes age-related macular degeneration. Cell Metab. 17, 549–561 (2013).

4. Fujinami, K. et al. Clinical and molecular characteristics of childhood-onset Stargardt disease. Ophthalmology 122, 326–334 (2015).

5. Molday, R. S., Zhong, M. & Quazi, F. The role of the photoreceptor ABC transporter ABCA4 in lipid transport and Stargardt macular degeneration. Biochim. Biophys. Acta 1791, 573–583 (2009).

6. Yamauchi, T. et al. Cloning of adiponectin receptors that mediate antidiabetic metabolic effects. Nature 423, 762–769 (2003).

7. Kadowaki, T. & Yamauchi, T. Adiponectin receptor signaling: a new layer to the current model. Cell Metab. 13, 123–124 (2011).

8. Okada-Iwabu, M., Iwabu, M., Yamauchi, T. & Kadowaki, T. Drug development research for novel adiponectin receptor-targeted antidiabetic drugs con- tributing to healthy longevity. Diabetol. Int. 10, 237–244 (2019).

9. Yu, X. H., Zhang, D. W., Zheng, X. L. & Tang, C. K. C1q tumor necrosis factor- related protein 9 in atherosclerosis: mechanistic insights and therapeutic potential. Atherosclerosis 276, 109–116 (2018).

10. Xu, M. et al. ADIPOR1 is mutated in syndromic retinitis pigmentosa. Hum. Mutat. 37, 246–249 (2016).

11. Zhang, J. et al. A mutation in ADIPOR1 causes nonsyndromic autosomal dominant retinitis pigmentosa. Hum. Genet. 135, 1375–1387 (2016).

12. Jastrzebska, B., Debinski, A., Filipek, S. & Palczewski, K. Role of membrane integrity on G protein-coupled receptors: rhodopsin stability and function. Prog. Lipid Res. 50, 267–277 (2011).

13. Mitchell, D. C., Niu, S. L. & Litman, B. J. Quantifying the differential effects of DHA and DPA on the early events in visual signal transduction. Chem. Phys. Lipids 165, 393–400 (2012).

14. Scott, B. L. & Bazan, N. G. Membrane docosahexaenoate is supplied to the developing brain and retina by the liver. Proc. Natl Acad. Sci. USA 86, 2903–2907 (1989).

15. Aveldano, M. I. Phospholipid species containing long and very long polyenoic fatty acids remain with rhodopsin after hexane extraction of photoreceptor membranes. Biochemistry 27, 1229–1239 (1988).

16. Rice, D. S. et al. Adiponectin receptor 1 conserves docosahexaenoic acid and promotes photoreceptor cell survival. Nat. Commun. 6, 6228 (2015).

17. Kautzmann, M. I. et al. Membrane-type frizzled-related protein regulates lipi- dome and transcription for photoreceptor function. FASEB J. 34, 912–929 (2020).

18. Jakobsson, A., Westerberg, R. & Jacobsson, A. Fatty acid elongases in mam- mals: their regulation and roles in metabolism. Prog. Lipid Res. 45, 237–249 (2006).

19. Bogie, J. F. J., Haidar, M., Kooij, G. & Hendriks, J. J. A. Fatty acid metabolism in the progression and resolution of CNS disorders. Adv. Drug Deliv. Rev. 159, 198–213 (2020).

20. Kawashima, H. et al. Neuroprotective and vision-protective effect of preserving ATP levels by AMPK activator. FASEB J. 34, 5016–5026 (2020).

21. Osada, H. et al. Neuroprotective effect of bilberry extract in a murine model of photo-stressed retina. PLoS ONE 12, e0178627 (2017).

22. Nagai, N. et al. Renin-angiotensin system impairs macrophage lipid metabo- lism to promote age-related macular degeneration in mouse models. Com- mun. Biol. 3, 767 (2020).

23. Ogawa, M. et al. Eosinophils promote corneal wound healing via the 12/15- lipoxygenase pathway. FASEB J. 34, 12492–12501 (2020).

24. Tsugawa, H. et al. A lipidome atlas in MS-DIAL 4. Nat. Biotechnol. 38, 1159–1163 (2020).

25. Naoe, S., Tsugawa, H., Takahashi, M., Ikeda, K. & Arita, M. Characterization of lipid profiles after dietary intake of polyunsaturated fatty acids using integrated untargeted and targeted lipidomics. Metabolites 9, 241 (2019).

26. Li, L. C. & Dahiya, R. MethPrimer: designing primers for methylation PCRs. Bioinformatics 18, 1427–1431 (2002).

27. Wong, B. H. et al. Mfsd2a is a transporter for the essential omega-3 fatty acid docosahexaenoic acid (DHA) in eye and is important for photoreceptor cell development. J. Biol. Chem. 291, 10501–10514 (2016).

28. Liu, C., Ye, D., Wang, H., He, M. & Sun, Y. Elovl2 but not Elovl5 is essential for the biosynthesis of docosahexaenoic acid (DHA) in zebrafish: insight from a comparative gene knockout study. Mar. Biotechnol. 22, 613–619 (2020).

29. Ikeda, M. et al. Characterization of four mammalian 3-hydroxyacyl-CoA dehydratases involved in very long-chain fatty acid synthesis. FEBS Lett. 582, 2435–2440 (2008).

30. Baehr, W. et al. Insights into photoreceptor ciliogenesis revealed by animal models. Prog. Retin Eye Res. 71, 26–56 (2019).

31. Sluch, V. M. et al. ADIPOR1 is essential for vision and its RPE expression is lost in the Mfrp(rd6) mouse. Sci. Rep. 8, 14339 (2018).

32. Narayan, D. S., Chidlow, G., Wood, J. P. & Casson, R. J. Glucose metabolism in mammalian photoreceptor inner and outer segments. Clin. Exp. Ophthalmol. 45, 730–741 (2017).

33. May-Simera, H. L. et al. Loss of MACF1 abolishes ciliogenesis and disrupts apicobasal polarity establishment in the retina. Cell Rep. 17, 1399–1413 (2016).

34. Hobson, A. H. et al. Apoptotic photoreceptor death in the rhodopsin knockout mouse in the presence and absence of c-fos. Exp. Eye Res. 71, 247–254 (2000).

35. Rajala, R. V. & Anderson, R. E. Rhodopsin-regulated insulin receptor signaling pathway in rod photoreceptor neurons. Mol. Neurobiol. 42, 39–47 (2010).

36. Bringmann, A. et al. Cellular signaling and factors involved in Muller cell gliosis: neuroprotective and detrimental effects. Prog. Retin Eye Res. 28, 423–451 (2009).

37. Agca, C. et al. p38 MAPK signaling acts upstream of LIF-dependent neuro- protection during photoreceptor degeneration. Cell Death Dis. 4, e785 (2013).

38. Ozawa, Y. Oxidative stress in the light-exposed retina and its implication in age-related macular degeneration. Redox Biol. 37, 101779 (2020).

39. Sasaki, M. et al. Neuroprotective effect of an antioxidant, lutein, during retinal inflammation. Invest. Ophthalmol. Vis. Sci. 50, 1433–1439 (2009).

40. Kamoshita, M., Fujinami, K., Toda, E., Tsubota, K. & Ozawa, Y. Neuro- protective effect of activated 5’-adenosine monophosphate-activated protein kinase on cone system function during retinal inflammation. BMC Neurosci. 17, 32 (2016).

41. Okamoto, T. et al. Dietary spirulina supplementation protects visual function from photostress by suppressing retinal neurodegeneration in mice. Transl. Vis. Sci. Technol. 8, 20 (2019).

42. Ait-Ali, N. et al. Rod-derived cone viability factor promotes cone survival by stimulating aerobic glycolysis. Cell 161, 817–832 (2015).

43. Fridlich, R. et al. The thioredoxin-like protein rod-derived cone viability factor (RdCVFL) interacts with TAU and inhibits its phosphorylation in the retina. Mol. Cell Proteom. 8, 1206–1218 (2009).

44. Leveillard, T. et al. Identification and characterization of rod-derived cone viability factor. Nat. Genet. 36, 755–759 (2004).

45. Pauter, A. M. et al. Elovl2 ablation demonstrates that systemic DHA is endo- genously produced and is essential for lipid homeostasis in mice. J. Lipid Res. 55, 718–728 (2014).

46. Zadravec, D. et al. ELOVL2 controls the level of n-6 28:5 and 30:5 fatty acids in testis, a prerequisite for male fertility and sperm maturation in mice. J. Lipid Res. 52, 245–255 (2011).

47. Chen, D. et al. The lipid elongation enzyme ELOVL2 is a molecular regulator of aging in the retina. Aging Cell 19, e13100 (2020).

48. Ding, Y. et al. MYCN and PRC1 cooperatively repress docosahexaenoic acid synthesis in neuroblastoma via ELOVL2. J. Exp. Clin. Cancer Res. 38, 498 (2019).

49. Bacalini, M. G. et al. Systemic age-associated DNA hypermethylation of ELOVL2 gene: in vivo and in vitro evidences of a cell replication process. J. Gerontol. A Biol. Sci. Med. Sci. 72, 1015–1023 (2017).

50. Li, X. et al. Impaired lipid metabolism by age-dependent DNA methylation alterations accelerates aging. Proc. Natl Acad. Sci. USA 117, 4328–4336 (2020).

51. Ruiz, M., Stahlman, M., Boren, J. & Pilon, M. AdipoR1 and AdipoR2 maintain membrane fluidity in most human cell types and independently of adipo- nectin. J. Lipid Res. 60, 995–1004 (2019).

52. Nguyen, L. N. et al. Mfsd2a is a transporter for the essential omega-3 fatty acid docosahexaenoic acid. Nature 509, 503–506 (2014).

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