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Morphological and Crystal-Chemical Features of Macro- and Microcalcifications of Human Aorta

Published online by Cambridge University Press:  15 September 2021

Inna-Margaryta Radomychelski
Affiliation:
Department of Pathology, Sumy State University, Sumy, Ukraine
Artem Piddubnyi
Affiliation:
Department of Pathology, Sumy State University, Sumy, Ukraine Ukrainian-Swedish Research Center SUMEYA, Sumy, Ukraine
Sergey Danilchenko
Affiliation:
Institute of Applied Physics, National Academy of Sciences of Ukraine, Sumy, Ukraine
Olena Maksymova
Affiliation:
Department of Morphology, Sumy State University, Sumy, Ukraine
Yuliia Moskalenko
Affiliation:
Department of Oncology, Sumy State University, Sumy, Ukraine
Roman Moskalenko*
Affiliation:
Department of Pathology, Sumy State University, Sumy, Ukraine Ukrainian-Swedish Research Center SUMEYA, Sumy, Ukraine
*
*Corresponding author: Roman Moskalenko, E-mail: [email protected]
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Abstract

Ectopic calcification or pathological biomineralization correlates with morbidity and mortality from cardiovascular diseases. Aortas with atherosclerotic lesions and biomineralization were selected for the study. Thirty samples of mineralized abdominal aortas (group M) were examined by histology. Depending on the calcifications size, samples were separated into group M1 (macroscopic calcifications) and M2 (microscopic calcifications). Each group consists of 15 samples. Calcification 2 mm or less were considered as microscopic, >2 mm—macroscopic. Thirty samples of aortic tissue without biomineralization (group C) were used as a control group. Aortic tissue was examined by macroscopic description, histology, histochemistry, immunohistochemistry (IHC), scanning electron microscopy (SEM) with microanalysis, and transmission electron microscopy (TEM). The results of IHC showed the involvement of OPN in the formation and development of pathological biomineralization, but the obvious role of OPN in the differentiation of macro- and microcalcifications of atherosclerotic aorta was not revealed. SEM with X-ray microanalysis confirmed that the biomineral part of the aortic samples of the M1 group consisted mainly of apatites, which correspond to previous studies. The Ca/P ratio was less in the M2 group than in the M1 group. It means that microcalcifications can be formed by more defective (immature) hydroxyapatite.

Type
Micrographia
Copyright
Copyright © The Author(s), 2021. Published by Cambridge University Press on behalf of the Microscopy Society of America

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References

Anderson, HC (1983). Calcific diseases. A concept. Archives of pathology & laboratory medicine 107(7), 341348.Google ScholarPubMed
Bakhshian Nik, A, Hutcheson, JD & Aikawa, E (2017). Extracellular vesicles as mediators of cardiovascular calcification. Front Cardiovasc Med 4(78), 17. doi:10.3389/fcvm.2017.00078CrossRefGoogle ScholarPubMed
Bertazzo, S, Gentleman, E, Cloyd, KI, Chester, AH, Yacoub, MH & Stevens, MM (2013). Nano-analytical electron microscopy reveals fundamental insights into human cardiovascular tissue calcification. Nat Mater 12(6), 576.CrossRefGoogle ScholarPubMed
Brown, AJ, Teng, Z, Evans, PC, Gillard, JH, Samady, H & Bennett, MR (2016). Role of biomechanical forces in the natural history of coronary atherosclerosis. Nat Rev Cardiol 13(4), 210220. doi:10.1038/nrcardio.2015.203.CrossRefGoogle ScholarPubMed
Curtze, SC, Kratz, M, Steinert, M & Vogt, S (2016). Step-down vascular calcification analysis using state-of-the-art nanoanalysis techniques. Sci Rep 6, 23285.CrossRefGoogle ScholarPubMed
Danilchenko, SN, Kalinkevich, AN, Moskalenko, RA, Kuznetsov, VN, Kochenko, AV, Husak, EV, Starikov, VV, Liu, F, Meng, J & Lu, J (2018). Structural and crystal-chemical characteristics of the apatite deposits from human aortic walls. Interv Med Appl Sci 10(2), 110119.Google ScholarPubMed
Danilchenko, SN, Kuznetsov, VN, Stanislavov, AS, Kalinkevich, AN, Starikov, VV, Moskalenko, RA, Kalinichenko, TG, Kochenko, AV, , J, Shang, J & Yang, S (2013). The mineral component of human cardiovascular deposits: Morphological, structural and crystal-chemical characterization. Cryst Res Technol 48(3), 153162.CrossRefGoogle Scholar
Hutcheson, JD, Goettsch, C, Bertazzo, S, Maldonado, N, Ruiz, JL, Goh, W, Yabusaki, K, Faits, T, Bouten, C, Franck, G, Quillard, T, Libby, P, Aikawa, M, Weinbaum, S & Aikawa, E (2016). Genesis and growth extracellular vesicle-derived microcalcification in atherosclerotic plagues. Nat Mater 15, 335343. doi:10.1038/nmat4519CrossRefGoogle Scholar
Hutcheson, JD, Goettsch, C, Pham, T, Iwashita, M, Aikawa, M, Singh, SA & Aikawa, E (2014). Enrichment of calcifying extracellular vesicles using density-based ultracentrifugation protocol. J Extracell Vesicles 3, 25129. doi:10.3402/jev.v3.25129.CrossRefGoogle ScholarPubMed
Li, Y, Wang, CQ, Lu, A-H, Li, K, Xiao, C, Chongqing, Y, Yanzhang, L, Yan, L & Ding, H-R (2020). A comparative study of pathological nanomineral aggregates with distinct morphology in human aortic atherosclerotic plagues. J Nanosci Nanotechnol 20, 18.Google Scholar
Lok, ZSY & Lyle, A (2019). Osteopontin in vascular disease: Friend or foe? Arterioscler Thromb Vasc Biol 39, 613622. doi:10.1161/ATVBAHA.118.311577CrossRefGoogle Scholar
Menini, S, Iacobini, C, Ricci, C, Blasetti Fantauzzi, C, Salvi, L, Pesce, CM, Relucenti, M, Familiari, G, Taurino, M & Pugliese, G (2013). The galectin-3/RAGE dyad modulates vascular osteogenesis in atherosclerosis. Cardiovasc Res 100(3), 472480. doi:10.1093/cvr/cvt206CrossRefGoogle ScholarPubMed
Moskalenko, R, Romaniuk, A, Iashchichyn, I, Zakorko, I-M, Piddubnyi, А, Chernov, Y & Morozova-Roche, L (2017). Involvement of proinflammatory S100A8/S100A9 in the atherocalcinosis of aortic valve. Patologia 14(1), 4956.Google Scholar
Otsuka, F, Sakakura, K, Yahaki, K, Joner, M & Virmani, R (2014). Has our understanding of calcification in human coronary atherosclerosis progressed? Arterioscl Thromb Vasc Biol 34, 724736.CrossRefGoogle ScholarPubMed
Pugliese, G, Iacobini, C, Blasetti Fantauzzi, C & Menini, S (2015). The dark and bright side of atherosclerotic calcification. Atherosclerosis 238(2), 220230. doi:10.1016/j.atherosclerosis.2014.12.011CrossRefGoogle Scholar
Rocha-Singh, KJ, Zeller, T & Jaff, MR (2014). Peripheral arterial calcification: Prevalence, mechanism, detection, and clinical implications. Catheter Cardiovasc Interv 83(6), E212E220. doi:10.1002/ccd.25387CrossRefGoogle ScholarPubMed
Shioi, A & Ikari, Y (2018). Plague calcification during atherosclerosis progression and regression. J Atheroscler Thromb 25, 294303. doi:10.5551/jat.RV17020CrossRefGoogle Scholar
Steiz, SA, Speer, MY, McKee, MD, Liaw, L, Almeida, M, Yang, H & Giachelli, CM (2002). Osteopontin inhibits mineral deposition and promotes regression of ectopic calcification. Am J Pathol 161(6), 20352046.CrossRefGoogle Scholar
van der Toorn, JE, Rueda-Ochoa, OL, van der Schaft, N, Vernooij, MW, Ikram, MA, Bos, D & Kavousi, M (2020). Arterial calcification at multiple sites: Sex-specific cardiovascular risk profiles and mortality risk – The Rotterdam Study. BMC Med 18(1), 263. doi:10.1186/s12916-020-01722-7CrossRefGoogle ScholarPubMed
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