Submissions are open for the upcoming issue.

Molecular Medicine Peer-reviewed scientific journal

Molecular Medicine

ОБЗОР2020, No. 4

HYALURONIC ACID: ROLE IN THE CELL CYCLE

Khabarov V.N., Belushkina N.N., Paltsev M.A., Kvetnoi I.M.

Authors and affiliations

V.N. Khabarov(1), N.N. Belushkina(2), M.A. Paltsev(2), I.M. Kvetnoi(3) 1-Research Center of hyaluronic acid, Komsomolsky Avenu, 38/16, Moscow, 119146, Russian Federation; 2-Lomonosov Moscow State University, Leninskie gory, 1/12, Moscow, 119991, Russian Federation; 3-Saint-Petersburg State Research Institute of Phthisiopulmonology, Ligovsky avenue, 2–4, Saint-Petersburg, 191036, Russian Federation E-mail: igor.kvetnoy@yandex.ru

Published
2020
Section
ОБЗОР
Issue2020, No. 4Go to the issue →
How to cite

Abstract

The review considers the system of hyaluronic acid (HA), represented by its receptors, the enzymes of synthesis (hyaluronan synthase), cleavage (hyaluronidase). The participation of the HA system in the regulation of the cell cycle was demonstrated. The most important HA receptor is the transmembrane protein CD44, whose intracellular domain is associated with cytoskeletal proteins. All components of the HA system include hyaluronan synthetases, hyaluronidases, and HA receptors are important participants in the cell cycle of normal and, to an even greater extent, precancerous and cancerous cells. Differences in the regulation of the cell cycle of HA both high-molecular and low-molecular fractions were demonstrated. High-molecular-weight HA supports differentiated and stem cells in the G0 cell cycle phase by blocking access to receptors. During embryogenesis, HA high-molecular-weight fraction activates PI3K-ACT and RAS-ERK cascades in cells of primary trophoblasts, leading to their active proliferation. On the proliferation of adult cells, high-molecular HA acid has the opposite, inhibitory effect due to the inhibitory effect of the Merlin protein. HA both low-molecular fractions and receptors are involved in the processes of the cell cycle after its initial initiation by proinflammatory factors. To activate the CD44 cytoplasmic domain with HA low-molecular-weight fractions, the Merlin protein must be detached from it. The use of HA in medical practice requires full consideration of these various modes of regulation.

Keywords

Authors and affiliations

V.N. Khabarov(1), N.N. Belushkina(2), M.A. Paltsev(2), I.M. Kvetnoi(3) 1-Research Center of hyaluronic acid, Komsomolsky Avenu, 38/16, Moscow, 119146, Russian Federation; 2-Lomonosov Moscow State University, Leninskie gory, 1/12, Moscow, 119991, Russian Federation; 3-Saint-Petersburg State Research Institute of Phthisiopulmonology, Ligovsky avenue, 2–4, Saint-Petersburg, 191036, Russian Federation E-mail: igor.kvetnoy@yandex.ru

References

Habarov V.N., Bojkov P.Ja., Seljanin M.A. Gialuronovaja kislota. M.: Prakticheskaja meditsina, 2012; 224. [Habarov V.N., Bojkov P.YA., Selyanin M.A. Hyaluronic acid. M.: Prakticheskaya medicina, 2012; 224 (in Russian)]

Habarov V.N., Bojkov P.Ja. Biohimija gialuronovoj kisloty. M.: Tiso-print, 2016; 288. [Habarov V.N., Bojkov P.YA., Selyanin M.A. Biochemistry of hyaluronic acid. M.: Tiso-print, 2016; 288 (in Russian)]

Habarov V.N., Ivanov P.L. Biomeditsinskoe primenenie gialuronovoj kisloty i ee himicheski modifitsirovannyh proizvodnyh. M.: GEOTAR-MED, 2019; 288. [Habarov V.N., Ivanov P.L. Biomedical application of hyaluronic acid and its chemically modified derivatives. M.: GEOTAR-MED, 2019; 288 (in Russian)]

Johnson P., Arif A.A., Lee-Sayer S.S.M., Dong Y. Hyaluronan and its interactions with immune cells in the healthy and inflamed lung. Front Immunol. 2018; 9: 2787. https://doi.org/10.3389/fimmu.2018.02787

Krolikoski M., Monslow J., Puré E. The CD44-HA axis and inflammation in atherosclerosis: A temporal perspective. Matrix Biol. 2019; 78/79: 201–18. https://doi.org/10.1016/j.matbio.2018.05.007

Liu R., Sun R., Zhang L., Zhang Q., Chen D., Zhong J., Xiao J. Hyaluronic acid enhances proliferation of human amniotic mesenchymal stem cells through activation of Wnt/β-catenin signaling pathway. Exp. Cell. Res. 2016; 345 (2): 218–29. https://doi.org/10.1016/j.yexcr.2016.05.019

Chen X., Du Y., Liu Y., He Y., Zhang G., Yang C., Gao F. Hyaluronan arrests human breast cancer cell growth by prolonging the G0/G1 phase of the cell cycle. Acta Biochim Biophys Sin (Shanghai). 2018; 50 (12): 1181–89. https://doi.org/10.1093/abbs/gmy126

Itano N., Kimata K. Mammalian hyaluronan synthases. IUBMB Life. 2002; 54 (4): 195–9. https://doi.org/10.1080/15216540214929

Vigetti D., Viola M., Karousou E., De Luca G., Passi A. Metabolic control of hyaluronan synthases. Matrix Biol. 2014; 35: 8–13. https://doi.org/10.1016/j.matbio.2013.10.002

Ohtsuki T., Asano K., Inagaki J., Shinaoka A., Kumagishi-Shinaoka K., Cilek M., Hatipoglu O., Oohashi T., Nishida K., Komatsubara I., Hirohata S. High molecular weight hyaluronan protects cartilage from degradation by inhibiting aggrecanase expression. J. Orthop Res. 2018; 36 (12): 3247–55. https://doi.org/10.1002/jor.24126

Cowman M., Shortt C., Arora S., Fu Y., Villavieja J., Rathore J., Huang X., Rakshit T., Jung G., Kirsch T. Role of Hyaluronan in Inflammatory Effects on Human Articular Chondrocytes. Inflammation. 2019; 42 (5): 1808–20. https://doi.org/10.1007/s10753-019-01043-9

Nagy N., Sunkari V.G., Kaber G., Hasbun S., Lam D.N., Speake C., Sanda S., McLaughlin T.L., Wight T., Long S., Bollyky P. Hyaluronan levels are increased systemically in human type 2 but not type 1 diabetes independently of glycemic control. Matrix Biol. 2019; 80: 46–58. https://doi.org/10.1016/j.matbio.2018.09.003

Törrönen K., Nikunen K., Kärnä R., Tammi M., Tammi R., Rilla K. Tissue distribution and subcellular localization of hyaluronan synthase isoenzymes. Histochem Cell Biol. 2014; 141 (1): 17–31. https://doi.org/10.1007/s00418-013-1143-4

Stuhlmeier K., Pollaschek C. Differential effect of transforming growth factor beta (TGF-beta) on the genes encoding hyaluronan synthases and utilization of the p38 MAPK pathway in TGF-beta-induced hyaluronan synthase 1 activation. J. Biol Chem. 2004; 279: 8753–60. https://doi.org/10.1074/jbc.M303945200

Rauhala L., Jokela T., Kärnä R., Bart G., Takabe P., Oikari S., Tammi M., Pasonen-Seppänen S., Tammi R. Extracellular ATP activates hyaluronan synthase 2 (HAS2) in epidermal keratinocytes via P2Y2, Ca2+ signaling, and MAPK pathways. Biochem J. 2018; 475 (10): 1755–72. https://doi.org/10.1042/BCJ20180054

Buhren B., Schrumpf H., Hoff N., Bölke E., Gerber P. Hyaluronidase: from clinical applications to molecular and cellular mechanisms. Eur. J. Med. Res. 2016; 21: 5. https://doi.org/10.1186/s40001-016-0201-5

Hida D., Danielson B., Knudson C., Knudson W. CD44 knock-down in bovine and human chondrocytes results in release of bound HYAL2. Matrix Biol. 2015; 48: 42. https://doi.org/10.1016/j.matbio.2015.04.002

Terazawa S., Nakajima H., Tobita K., Imokawa G. The decreased secretion of hyaluronan by older human fibroblasts under physiological conditions is mainly associated with the down-regulated expression of hyaluronan synthases but not with the expression levels of hyaluronidases. Cytotechnology. 2015; 67: 609–20. https://doi.org/10.1007/s10616-014-9707-2

Qu C., Rilla K., Tammi R., Tammi M., Kröger H., Lammi M. Extensive CD44-dependent hyaluronan coats on human bone marrow-derived mesenchymal stem cells produced by hyaluronan synthases HAS1, HAS2 and HAS3. Int J. Biochem Cell Biol. 2014; 48: 45–54. https://doi.org/10.1016/j.biocel.2013.12.016

Knudson W., Ishizuka S., Terabe K., Askew E., Knudson C. The pericellular hyaluronan of articular chondrocytes. Matrix Biol. 2019; 78/79: 32–46. https://doi.org/10.1016/j.matbio.2018.02.005

Harris E., Cabral F. Ligand Binding and Signaling of HARE/Stabilin-2. Biomolecules. 2019; 9 (7): 273. https://doi.org/10.3390/biom9070273

Marcotti S., Maki K., Reilly G.C., Lacroix D., Adachi T. Hyaluronic acid selective anchoring to the cytoskeleton: An atomic force microscopy study. PLoS One. 2018; 13 (10): e0206056. https://doi.org/10.1371/journal.pone.0206056

Dhar D., Antonucci L., Nakagawa H., Kim J., Glitzner E., Caruso S., Karin M. Liver Cancer Initiation Requires p53 Inhibition by CD44-Enhanced Growth Factor Signaling. Cancer Cell. 2018; 33 (6): 1061–77. https://doi.org/10.1016/j.ccell.2018.05.003

Murai T. Lipid Raft-Mediated Regulation of Hyaluronan-CD44 Interactions in Inflammation and Cancer. Front Immunol. 2015; 6: 420. https://doi.org/10.3389/fimmu.2015.00420

Janiszewska M., De Vito C., Le Bitoux M., Fusco C., Stamenkovic I. Transportin regulates nuclear import of CD44. J. Biol. Chem. 2010; 285 (40): 30548–57. https://doi.org/10.1074/jbc.M109.075838

Arasu U., Kärnä R., Härkönen K., Oikari S., Koistinen A., Kröger H., Qu C., Lammi M., Rilla K. Human mesenchymal stem cells secrete hyaluronan-coated extracellular vesicles. Matrix Biol. 2017; 64: 54–8. https://doi.org/10.1016/j.matbio.2017.05.001

Pandey M., Baggenstoss B., Washburn J., Harris E., Weigel P. The hyaluronan receptor for endocytosis (HARE) activates NF-κB-mediated gene expression in response to 40-400-kDa, but not smaller or larger, hyaluronans. J. Biol. Chem. 2013; 288 (20): 14068–79. https://doi.org/10.1074/jbc.M112.442889

Morgan D. The cell cycle: principles of control. Yale J. Biol. Med. 2007; 80 (3): 141–42.

Morrish F., Isern N., Sadilek M., Jeffrey M., Hockenbery D. c-Myc activates multiple metabolic networks to generate substrates for cell-cycle entry. Oncogene. 2009; 28 (27): 2485–91. https://doi.org/10.1038/onc.2009.112

Pandey N., Vinod P.K. Mathematical modelling of reversible transition between quiescence and proliferation. PLoS One. 2018; 13 (6): e0198420. https://doi.org/10.1371/journal.pone.0198420

Zwang Y., Sas-Chen A., Drier Y., Shay T., Avraham R., Lauriola M., Shema E., Lidor-Nili E., Jacob-Hirsch J., Yarden Y. Two phases of mitogenic signaling unveil roles for p53 and EGR1 in elimination of inconsistent growth signals. Mol Cell. 2011; 42: 524–35. https://doi.org/10.1016/j.molcel.2011.04.017

Xu N., Lao Y., Zhang Y., Gillespie D.A. Akt: a double-edged sword in cell proliferation and genome stability. J. Oncol. 2012; 2012: 951724.

Lee H., Jeong A., Ye S. Highlighted STAT3 as a potential drug target for cancer therapy. BMB Rep. 2019; 52 (7): 415–23. https://doi.org/10.5483/BMBRep.2019.52.7.152

Bahrami S., Drabløs F. Gene regulation in the immediate-early response process. Adv Biol Regul. 2016; 62: 37–49.

Blanchet E., Annicotte J., Lagarrigue S., Aguilar V., Clapé C., Chavey C., Fritz V., Casas F., Apparailly F., Auwerx J., Fajas L. E2F transcription factor-1 regulates oxidative metabolism. Nat Cell Biol. 2011; 13 (9): 1146–52. https://doi.org/10.1038/ncb2309

Godar S., Weinberg R. Filling the mosaic of p53 actions: p53 represses RHAMM expression. Cell Cycle. 2008; 7 (22): 3479. https://doi.org/10.4161/cc.7.22.7320

Inoue K., Fry E. Tumor suppression by the EGR1, DMP1, ARF, p53, and PTEN network. Cancer Invest. 2018; 36 (99–10): 520–36. https://doi.org/10.1080/07357907.2018.1533965

Heldin P., Basu K., Kozlova I., Porsch H. HAS2 and CD44 in breast tumorigenesis. Adv Cancer Res. 2014; 123: 211–29. https://doi.org/10.1016/B978-0-12-800092-2.00008-3

Liu M., Tolg C., Turley E. Dissecting the Dual Nature of Hyaluronan in the Tumor Microenvironment. Front Immunol. 2019; 10: 947. https://doi.org/10.3389/fimmu.2019.00947

Mowbray C., Shams S., Chung G., Stanton A., Aldridge P., Suchenko A., Pickard R., Ali A., Hall J. High molecular weight hyaluronic acid: a two-pronged protectant against infection of the urogenital tract? Clin Transl Immunology. 2018; 7 (6): e1021. https://doi.org/10.1002/cti2.1021

Zhu R., Huang Y., Tao Y., Wang S., Sun C., Piao H., Wang X. Hyaluronan up-regulates growth and invasion of trophoblasts in an autocrine manner via PI3K/AKT and MAPK/ERK1/2 pathways in early human pregnancy. Placenta. 2013; 34 (9): 784–91. https://doi.org/10.1016/j.placenta.2013.05.009

Kothapalli D., Flowers J., Assoian R. Differential activation of ERK and Rac mediates the pro-liferative and anti-proliferative effects of hyaluronan and CD44. J. Biol. Chem. 2008; 283 (46): 31823–9 https://doi.org/10.1074/jbc.M802934200

Evanko S., Potter-Perigo S., Petty L., Workman G., Wight T. Hyaluronan Controls the Deposition of Fibronectin and Collagen and Modulates TGF-β1 Induction of Lung Myofibroblasts. Matrix Biol. 2015; 42: 74–92. https://doi.org/10.1016/j.matbio.2014.12.001

Puré E., Assoian R. Rheostatic signaling by CD44 and hyaluronan. Cell Signal. 2009; 21 (5): 651–5. https://doi.org/10.1016/j.cellsig.2009.01.024

Cyphert J., Trempus C., Garantziotis S. Size Matters: Molecular Weight Specificity of Hyaluronan Effects in Cell Biology. Int J. Cell. Biol. 2015; 2015: 563818.

Heldin P., Lin C., Kolliopoulos C., Chen Y., Skandalis S. Regulation of hyaluronan biosynthesis and clinical impact of excessive hyaluronan production. Matrix Biol. 2019; 78–79: 100–17. https://doi.org/10.1016/j.matbio.2018.01.017

Rayahin J., Buhrman J., Zhang Y., Gemeinhart R. High and low molecular weight hyaluronic acid differentially influence macrophage activation. ACS Biomater Sci Eng. 2015; 1 (7): 481–93. https://doi.org/10.1021/acsbiomaterials.5b00181

Albano G., Bonanno A., Cavalieri L., Ingrassia E., Di Sano C., Siena L., Riccobono L., Gagliardo R., Profita M. Effect of High, Medium, and Low Molecular Weight Hyaluronan on Inflammation and Oxidative Stress in an In Vitro Model of Human Nasal Epithelial Cells. Mediators Inflamm. 2016: 8727289. https://doi.org/10.1155/2016/8727289

Meran S., Luo D., Simpson R., Martin J., Wells A., Steadman R., Phillips A. Hyaluronan facilitates transforming growth factor-β1-dependent proliferation via CD44 and epidermal growth factor receptor interaction. J. Biol. Chem. 2011; 286: 17618–30. https://doi.org/10.1074/jbc.M111.226563

Kuo Y., Fang W., Huang C., Tsai S., Wang Y., Yang C., Wu L. Hyaluronan synthase 3 mediated oncogenic action through forming inter-regulation loop with tumor necrosis factor alpha in oral cancer. Oncotarget. 2017; 8: 15563–83. https://doi.org/10.18632/oncotarget.14697

Gao F., Yang C., Mo W., Liu Y., He Y. Hyaluronan oligosaccharides are potential stimulators to angiogenesis via RHAMM mediated signal pathway in wound healing. Clin Invest Med. 2008; 31 (3): 106–16. https://doi.org/10.25011/cim.v31i3.3467

Bauer J., Rothley M., Schmaus A., Quagliata L., Ehret M., Biskup M., Orian-Rousseau V. TGFβ counteracts LYVE-1-mediated induction of lymphangiogenesis by small hyaluronan oligosaccharides. J. Mol. Med. (Berl). 2018; 96 (2): 199–209.

Kim Y., Lee Y., Choe J., Lee H., Kim Y., Jeoung D. CD44-EGFR interaction mediates hyaluronic acid-promoted cell motility by activating protein kinase C signaling involving Akt, Rac1, Phox, reactive oxygen species, focal adhesion kinase, and MMP-2. J. Biol. Chem. 2008; 283 (33): 22513–28.

Schmitz I., Ariyoshi W., Takahashi N., Knudson W. Hyaluronan oligosaccharide treatment of chondrocytes stimulates expression of both HAS-2 and MMP-3, but by different signaling pathways. Osteoarthritis Cartilage. 2010; 18: 447–54. https://doi.org/10.1016/j.joca.2009.10.007

Nam K., Oh S., Lee K., Yoo S., Shin I. CD44 regulates cell proliferation, migration, and invasion via modulation of c-Src transcription in human breast cancer cells. Cell Signal. 2015; 27 (9): 1882–94. https://doi.org/10.1016/j.cellsig.2015.05.002

Avenoso A., Bruschetta G., D’Ascola A., Scuruchi M., Mandraffino G., Gullace R., Saitta A., Campo S. Hyaluronan fragments produced during tissue injury: A signal amplifying the inflammatory response. Arch Biochem Biophys. 2019; 663: 228–38. https://doi.org/10.1016/j.abb.2019.01.015

Khurana S., Riehl T., Moore B., Fassan M., Rugge M., Romero-Gallo J., Noto J., Peek R.Jr., Stenson W., Mills J. The hyaluronic acid receptor CD44 coordinates normal and metaplastic gastric epithelial progenitor cell proliferation. J. Biol. Chem. 2013; 288 (22): 16085–97. https://doi.org/10.1074/jbc.M112.445551

Nishida-Fukuda H., Araki R., Shudou M., Okazaki H., Tomono Y., Nakayama H., Fukuda S., Sakaue T., Shirakata Y., Sayama K., Hashimoto K., Detmar M., Higashiyama S., Hirakawa S. Ectodomain Shedding of Lymphatic Vessel Endothelial Hyaluronan Receptor 1 (LYVE-1) Is Induced by Vascular Endothelial Growth Factor A (VEGF-A). J. Biol. Chem. 2016; 291 (20): 10490–500. https://doi.org/10.1074/jbc.M115.683201

Lichtenthaler S., Lemberg M.K., Fluhrer R. Proteolytic ectodomain shedding of membrane proteins in mammals-hardware, concepts, and recent developments. EMBO J. 2018; 37 (15): e99456. https://doi.org/10.15252/embj.201899456

Carpenter G., Pozzi A. Cell responses to growth factors: the role of receptor tyrosine kinase intracellular domain fragments. Sci Signal. 2012; 5 (243): 42. https://doi.org/10.1126/scisignal.2003526

Merilahti J., Elenius K. Gamma-secretase-dependent signaling of receptor tyrosine kinases. Oncogene. 2019; 38 (2): 151–63. https://doi.org/10.1038/s41388-018-0465-z

Miletti-González K., Murphy K., Kumaran M., Ravindranath A., Wernyj R. Identification of function for CD44 intracytoplasmic domain (CD44-ICD): modulation of matrix metalloproteinase 9 (MMP-9) transcription via novel promoter response element. J. Biol. Chem. 2012; 287 (23): 18995–9007. https://doi.org/10.1074/jbc.M111.318774

Su M., Wang P., Wang X., Zhang M., Wei S., Liu K., Han S., Han X., Deng Y., Shen L. Nuclear CD44 Mediated by Importin β Participated in Naive Genes Transcriptional Regulation in C3A-iCSCs. Int J. Biol. Sci. 2019; 15 (6): 1252–60. https://doi.org/10.7150/ijbs.28235

Park D., Kim Y., Kim H., Kim K., Lee Y., Choe J., Hahn J., Lee H., Jeon J., Choi C., Kim Y., Jeoung D. Hyaluronic acid promotes angiogenesis by inducing RHAMM-TGFβ receptor interaction via CD44-PKCδ. Mol Cells. 2012; 33 (6): 563–74. https://doi.org/10.1007/s10059-012-2294-1

Grass G., Tolliver L., Bratoeva M., Toole B. CD147, CD44, and the epidermal growth factor receptor (EGFR) signaling pathway cooperate to regulate breast epithelial cell invasiveness. J. Biol. Chem. 2013; 288 (36): 26089–104. https://doi.org/10.1074/jbc.M113.497685

Nikitovic D., Kouvidi K., Karamanos N., Tzanakakis G. The roles of hyaluronan/RHAMM/CD44 and their respective interactions along the insidious pathways of fibrosarcoma progression. Biomed Res Int. 2013; 2013: 929531. https://doi.org/10.1155/2013/929531

Yoo B., Gredler R., Chen D., Santhekadur P., Fisher P., Sarkar D. S-Met activation through a novel pathway involving osteopontin mediates oncogenesis by the transcription factor LSF. J. Hepatol. 2011; 55 (6): 1317–24. https://doi.org/10.1016/j.jhep.2011.02.036

Chu Q., Huang H., Huang T., Cao L., Peng L., Shi S., Zheng L., Xu L., Zhang S., Huang J., Li X., Qian C., Huang B. Extracellular serglycin upregulates the CD44 receptor in an autocrine manner to maintain self-renewal in nasopharyngeal carcinoma cells by reciprocally activating the MAPK/β-catenin axis. Cell Death Dis. 2016; 7: e2456. https://doi.org/10.1038/cddis.2016.287

How to cite

Khabarov V.N., Belushkina N.N., Paltsev M.A., Kvetnoi I.M. (2020). HYALURONIC ACID: ROLE IN THE CELL CYCLE. Molecular Medicine, (4). https://doi.org/10.29296/24999490-2020-04-03

Article search and quick navigation

Navigation