Natural Products and Bioprospecting ›› 2026, Vol. 16 ›› Issue (5): 74-74.DOI: 10.1007/s13659-026-00609-z
• REVIEWS • Previous Articles Next Articles
Xue-Fang Zhao1,2, Zhou-Wei Wu2, Xiao-Qiu Liu1, Ming-Hua Qiu1,2,3
Received:2025-12-03
Accepted:2026-02-10
Online:2026-10-08
Supported by:Xue-Fang Zhao1,2, Zhou-Wei Wu2, Xiao-Qiu Liu1, Ming-Hua Qiu1,2,3
通讯作者:
Xiao-Qiu Liu,E-mail:liuxiaoqiu3388@126.com;Ming-Hua Qiu,E-mail:mhchiu@mail.kib.ac.cn
基金资助:Xue-Fang Zhao, Zhou-Wei Wu, Xiao-Qiu Liu, Ming-Hua Qiu. Maca polysaccharides: structural diversity, biological activities, and structure-activity relationships[J]. Natural Products and Bioprospecting, 2026, 16(5): 74-74.
Xue-Fang Zhao, Zhou-Wei Wu, Xiao-Qiu Liu, Ming-Hua Qiu. Maca polysaccharides: structural diversity, biological activities, and structure-activity relationships[J]. 应用天然产物, 2026, 16(5): 74-74.
| [1] Chen R, Wei J, Gao Y. A review of the study of active components and their pharmacology value in Lepidium meyenii (Maca). Phytother Res. 2021;35:6706–19. https://doi.org/10.1002/ptr.7257. [2] Lee H, Lee M, Qu F, Lee J, Kim E. Maca (Lepidium meyenii Walp.) on semen quality parameters: a systematic review and meta-analysis. Front Pharmacol. 2022;13:934740. https://doi.org/10.3389/fphar.2022.934740. [3] Huang YJ, Peng XR, Qiu MH. Progress on the chemical constituents derived from glucosinolates in maca (Lepidium meyenii). Nat Prod Bioprospect. 2018;8:405–12. https://doi.org/10.1007/s13659-018-0185-7. [4] Wang S, Zhu F. Chemical composition and health effects of maca (Lepidium meyenii). Food Chem. 2019;288:422–43. https://doi.org/10.1016/j.foodchem.2019.02.071. [5] Li K, Zhao C, Dang M, Ren R, Fu M, Bai Y, et al. Global research status of maca (Lepidium meyenii Walp.): a bibliometric analysis of hotspots, bursts, and trends. Drug Des Devel Ther. 2025;19:2329–49. https://doi.org/10.2147/dddt.S499849. [6] Meissner H, Mscisz A, Kedzia B, Pisulewski P, Pi?tkowska E. Peruvian maca: two scientific names Lepidium meyenii Walpers and Lepidium peruvianum Chacon-are they phytochemically-synonymous? Int J Biomed Sci. 2015;11:1–15. https://doi.org/10.59566/IJBS.2015.11001. [7] Ulloa Del Carpio N, Alvarado-Corella D, Qui?ones-Laveriano DM, Araya-Sibaja A, Vega-Baudrit J, Monagas-Juan M, et al. Exploring the chemical and pharmacological variability of Lepidium meyenii: a comprehensive review of the effects of maca. Front Pharmacol. 2024;15:1360422. https://doi.org/10.3389/fphar.2024.1360422. [8] Gong H, Li W, Sun J, Jia L, Guan Q, Guo Y, et al. A review on plant polysaccharide based on drug delivery system for construction and application, with emphasis on traditional Chinese medicine polysaccharide. Int J Biol Macromol. 2022;211:711–28. https://doi.org/10.1016/j.ijbiomac.2022.05.087. [9] Wu L, Zhang M, Xin X, Lai F, Wu H. Physicochemical and functional properties of a protein isolate from maca (Lepidium meyenii) and the secondary structure and immunomodulatory activity of its major protein component. Food Funct. 2019;10:2894–905. https://doi.org/10.1039/c8fo02490a. [10] Zhu H, Hu B, Hua H, Liu C, Cheng Y, Guo Y, et al. Macamides: a review of structures, isolation, therapeutics and prospects. Food Res Int. 2020;138:109819. https://doi.org/10.1016/j.foodres.2020.109819. [11] Zhou B, Chen Y, Luo H, Qi J, Yu B. Effect of maca (Lepidium meyenii) extract on non-obstructive azoospermia in male mice. J Ethnopharmacol. 2023;307:116228. https://doi.org/10.1016/j.jep.2023.116228. [12] da Silva Leitao Peres N, Cabrera Parra Bortoluzzi L. Medicinal effects of Peruvian maca (Lepidium meyenii): a review. Food Funct. 2020;11:83–92. https://doi.org/10.1039/c9fo02732g. [13] Tang W, Jin L, Xie L, Huang J, Wang N, Chu B, et al. Structural characterization and antifatigue effect in vivo of maca (Lepidium meyenii Walp) polysaccharide. J Food Sci. 2017;82:757–64. https://doi.org/10.1111/1750-3841.13619. [14] Wu J, Mo J, Xiang W, Shi X, Guo L, Li Y, et al. Immunoregulatory effects of Tetrastigma hemsleyanum polysaccharide via TLR4-mediated NF-κB and MAPK signaling pathways in RAW264.7 macrophages. Biomed Pharmacother. 2023;161:114471. https://doi.org/10.1016/j.biopha.2023.114471. [15] Zhang M, Wang G, Lai F, Wu H. Structural characterization and immunomodulatory activity of a novel polysaccharide from Lepidium meyenii. J Agric Food Chem. 2016;64:1921–31. https://doi.org/10.1021/acs.jafc.5b05610. [16] Li Y, Xu F, Zheng M, Xi X, Cui X, Han C. Maca polysaccharides: a review of compositions, isolation, therapeutics and prospects. Int J Biol Macromol. 2018;111:894–902. https://doi.org/10.1016/j.ijbiomac.2018.01.059. [17] Li Y, Xin Y, Xu F, Zheng M, Xi X, Cui X, et al. Maca polysaccharides: extraction optimization, structural features and anti-fatigue activities. Int J Biol Macromol. 2018;115:618–24. https://doi.org/10.1016/j.ijbiomac.2018.04.063. [18] Lee YK, Jung SK, Chang YH. Rheological properties of a neutral polysaccharide extracted from maca (Lepidium meyenii Walp.) roots with prebiotic and anti-inflammatory activities. Int J Biol Macromol. 2020;152:757–65. https://doi.org/10.1016/j.ijbiomac.2020.02.307. [19] Zhou H, Wubuli A, Wu Y, Lv Z, Li J. Research progress of polysaccharide structure-activity relationship. Food Sci Hum Wellness. 2025. https://doi.org/10.26599/FSHW.2025.9250485. [20] Li F, Jian Z, Rui Y, Tao A. Extraction, purification, structural features and biological activities of the Opuntia dillenii polysaccharides: a review. Int J Biol Macromol. 2025;314:144253. https://doi.org/10.1016/j.ijbiomac.2025.144253. [21] Xue H, Li P, Bian J, Gao Y, Sang Y, Tan J. Extraction, purification, structure, modification, and biological activity of traditional Chinese medicine polysaccharides: a review. Front Nutr. 2022;9:1005181. https://doi.org/10.3389/fnut.2022.1005181. [22] Wang C, Xu L, Huang L, Li X, Han W, Liu D, et al. Optimization of maca polysaccharide extraction process and its chemo-protective effects on cyclophosphamide-induced mice. J Food Process Eng. 2018;41:e12856. https://doi.org/10.1111/jfpe.12856. [23] Chen X, Sun-Waterhouse D, Yao W, Li X, Zhao M, You L. Free radical-mediated degradation of polysaccharides: mechanism of free radical formation and degradation, influence factors and product properties. Food Chem. 2021;365:130524. https://doi.org/10.1016/j.foodchem.2021.130524. [24] Guo L, Kong N, Zhang X, Haile. Multimode ultrasonic extraction of polysaccharides from maca (Lepidium meyenii): optimization, purification, and in vitro immunoregulatory activity. Ultrason Sonochem. 2022;88:106062. https://doi.org/10.1016/j.ultsonch.2022.106062. [25] Liu Y, Wang S, Yu X, Wang L, Meng Q, Wu J, et al. Optimization of ultrasonic-assisted extraction for enhancing the cosmetic potential and structural characterization of polysaccharide-rich extract from waste stem of Trollius chinensis Bunge. Ultrason Sonochem. 2025;120:107441. https://doi.org/10.1016/j.ultsonch.2024.107441. [26] Li J, Ye G, Wang J, Gong T, Wang J, Zeng D, et al. Recent advances in pressurized hot water extraction/modification of polysaccharides: structure, physicochemical properties, bioactivities, and applications. Compr Rev Food Sci Food Saf. 2025;24:e70104. https://doi.org/10.1111/1541-4337.70104. [27] Chao W, Jing L, Yi C, Jialu H, Hongyi L, Tiantian Z, et al. Extraction and characterization of pectic polysaccharides from Choerospondias axillaris peels: comparison of hot water and ultrasound-assisted extraction methods. Food Chem. 2022;401:134156. https://doi.org/10.1016/j.foodchem.2022.134156. [28] Farinaz G, Taghi GSM, Alaleh Z, Mehrdad M, Reza H. Microwave-assisted extraction of arabinan-rich pectic polysaccharides from melon peels: optimization, purification, bioactivity, and techno-functionality. Carbohydr Polym. 2021;256:117522. https://doi.org/10.1016/j.carbpol.2020.117522. [29] Hu W, Zhao Y, Yang Y, Zhang H, Ding C, Hu C, et al. Microwave-assisted extraction, physicochemical characterization and bioactivity of polysaccharides from Camptotheca acuminata fruits. Int J Biol Macromol. 2019;133:127–36. https://doi.org/10.1016/j.ijbiomac.2019.04.078. [30] Yadav N, Sharma S, Joys JS, Kumar S. Microwave assisted extraction of bioactive compounds: a brief review. J Indian Chem Soc. 2020;97:1751–6. [31] Luo C, Zhang H, Zheng H, Zhang J, Gan J. Optimization of glucosinolates extracted from maca (Lepidium meyenii) by combined ultrasonic and microwave extraction with response surface methodology. Adv Mater Res. 2012;550:1893–9. https://doi.org/10.4028/www.scientific.net/AMR.550-553.1893. [32] Zhang H, Cai X, Tian Q, Xiao L, Zeng Z, Cai X, et al. Microwave-assisted degradation of polysaccharide from Polygonatum sibiricum and antioxidant activity. J Food Sci. 2019;84:754–61. https://doi.org/10.1111/1750-3841.14449. [33] Jing Y, Yan M, Zhang H, Liu D, Qiu X, Hu B, et al. Effects of extraction methods on the physicochemical properties and biological activities of polysaccharides from Polygonatum sibiricum. Foods. 2023;12:2088. https://doi.org/10.3390/foods12102088. [34] Kim EJ, Yoon KY. Effects of different extraction methods on the physicochemical properties and biological activities of polysaccharides from maca roots. CyTA J Food. 2023;21:596–605. https://doi.org/10.1080/19476337.2023.2252879. [35] Yahaya N, Mohamed AH, Sajid M, Zain NNM, Liao PC, Chew KW. Deep eutectic solvents as sustainable extraction media for extraction of polysaccharides from natural sources: status, challenges and prospects. Carbohydr Polym. 2024;338:122199. https://doi.org/10.1016/j.carbpol.2024.122199. [36] Kim EJ, Kim CY, Yoon KY. Application of Taguchi method to optimize deep eutectic solvent-based ultrasound-assisted extraction of polysaccharides from maca and its biological activity. Food Bioprocess Technol. 2024;18:2709–20. https://doi.org/10.1007/s11947-024-03625-4. [37] Wang YY, Ma H, Ding ZC, Yang Y, Wang WH, Zhang HN, et al. Three-phase partitioning for the direct extraction and separation of bioactive exopolysaccharides from the cultured broth of Phellinus baumii. Int J Biol Macromol. 2019;123:201–9. https://doi.org/10.1016/j.ijbiomac.2018.11.065. [38] Wu ZW, Peng XR, Quan CX, Liu XC, Tao XY, Qiu MH. Structural characterization of six new Lepidium meyenii polysaccharides and their effects on gut microbiota in vitro. Int J Biol Macromol. 2025;319:145676. https://doi.org/10.1016/j.ijbiomac.2025.145676. [39] Wu ZW, Peng XR, Liu XC, Wen L, Tao XY, Al-Romaima A, et al. The structures of two polysaccharides from Lepidium meyenii and their immunomodulatory effects via activating NF-κB signaling pathway. Int J Biol Macromol. 2024;269:131761. https://doi.org/10.1016/j.ijbiomac.2024.131761. [40] Chen Y, Li Y, Zheng M, Feng K, Li J, Zhang Y, et al. Effect of step alcohol precipitation on compositions and antioxidant activity of maca polysaccharide. Chin J Exp Tradit Med Form. 2017;23:47–51. [41] Wang W, Zou Y, Li Q, Mao R, Shao X, Jin D, et al. Immunomodulatory effects of a polysaccharide purified from Lepidium meyenii Walp. on macrophages. Process Biochem. 2016;51:542–53. https://doi.org/10.1016/j.procbio.2016.01.003. [42] Li J, Sun Q, Meng Q, Wang L, Xiong W, Zhang L. Anti-fatigue activity of polysaccharide fractions from Lepidium meyenii Walp. (maca). Int J Biol Macromol. 2017;95:1305–11. https://doi.org/10.1016/j.ijbiomac.2016.11.031. [43] Wen L, Wu ZW, Lin LW, Al-Romaima A, Peng XR, Qiu MH. Structural characterizations and α-glucosidase inhibitory activities of four Lepidium meyenii polysaccharides with different molecular weights. Nat Prod Bioprospect. 2023;13:18. https://doi.org/10.1007/s13659-023-00384-1. [44] Zha Z, Wang SY, Chu W, Lv Y, Kan H, Chen Q, et al. Isolation, purification, structural characterization and immunostimulatory activity of water-soluble polysaccharides from Lepidium meyenii. Phytochemistry. 2018;147:184–93. https://doi.org/10.1016/j.phytochem.2018.01.006. [45] Zhang M, Wu W, Ren Y, Li X, Tang Y, Min T, et al. Structural characterization of a novel polysaccharide from Lepidium meyenii (maca) and analysis of its regulatory function in macrophage polarization in vitro. J Agric Food Chem. 2017;65:1146–57. https://doi.org/10.1021/acs.jafc.6b05218. [46] Wu Z, Zhao X, Quan C, Liu XC, Tao X, Li YJ, et al. Structure–function insights of natural Ganoderma polysaccharides: advances in biosynthesis and functional food applications. Nat Prod Bioprospect. 2025;15:15. https://doi.org/10.1007/s13659-025-00496-w. [47] Wang W, Zhang F, Li Q, Chen H, Zhang W, Yu P, et al. Structure characterization of one polysaccharide from Lepidium meyenii Walp., and its antioxidant activity and protective effect against H2O2-induced injury RAW264.7 cells. Int J Biol Macromol. 2018;118:816–33. https://doi.org/10.1016/j.ijbiomac.2018.06.117. [48] Saeidy S, Petera B, Pierre G, Fenoradosoa TA, Djomdi D, Michaud P, et al. Plants arabinogalactans: from structures to physico-chemical and biological properties. Biotechnol Adv. 2021;53:107771. https://doi.org/10.1016/j.biotechadv.2021.107771. [49] Ghosh K, Takahashi D, Kotake T. Plant type II arabinogalactan: structural features and modification to increase functionality. Carbohydr Res. 2023;529:108828. https://doi.org/10.1016/j.carres.2023.108828. [50] Li S, Hao L, Kang Q, Cui Y, Jiang H, Liu X, et al. Purification, characterization and biological activities of a polysaccharide from Lepidium meyenii leaves. Int J Biol Macromol. 2017;103:1302–10. https://doi.org/10.1016/j.ijbiomac.2017.05.165. [51] Mukherjee S, Jana S, Khawas S, Kicuntod J, Marschall M, Ray B, et al. Synthesis, molecular features and biological activities of modified plant polysaccharides. Carbohydr Polym. 2022;289:119299. https://doi.org/10.1016/j.carbpol.2022.119299. [52] Fu YL, Shi L. Methods of study on conformation of polysaccharides from natural products: a review. Int J Biol Macromol. 2024;263:130275. https://doi.org/10.1016/j.ijbiomac.2024.130275. [53] Goubet F, Barton CJ, Mortimer JC, Yu X, Zhang Z, Miles GP, et al. Cell wall glucomannan in Arabidopsis is synthesised by CSLA glycosyltransferases, and influences the progression of embryogenesis. Plant J. 2009;60(3):527–38. https://doi.org/10.1111/j.1365-313X.2009.03977.x. [54] Yu L, Yoshimi Y, Cresswell R, Wightman R, Lyczakowski JJ, Wilson LFL, et al. Eudicot primary cell wall glucomannan is related in synthesis, structure, and function to xyloglucan. Plant Cell. 2022;34:4600–22. https://doi.org/10.1093/plcell/koac238. [55] Amos RA, Mohnen D. Critical review of plant cell wall matrix polysaccharide glycosyltransferase activities verified by heterologous protein expression. Front Plant Sci. 2019;10:915. https://doi.org/10.3389/fpls.2019.00915. [56] Fei WT, Yue N, Li AM, Yu SH, Zhao DP, Zhu YL, et al. Immunomodulatory effects of Lepidium meyenii Walp. polysaccharides on an immunosuppression model induced by cyclophosphamide. J Immunol Res. 2022;2022:1210890. https://doi.org/10.1155/2022/1210890. [57] Fei W, Hou Y, Yue N, Zhou X, Wang Y, Wang L, et al. The effects of aqueous extract of maca on energy metabolism and immunoregulation. Eur J Med Res. 2020;25:24. https://doi.org/10.1186/s40001-020-00420-7. [58] Chang Y, Lu W, Chu Y, Yan J, Wang S, Xu H, et al. Extraction of polysaccharides from maca: characterization and immunoregulatory effects on CD4? T cells. Int J Biol Macromol. 2020;154:477–85. https://doi.org/10.1016/j.ijbiomac.2020.03.098. [59] Cao F, Zhang H, Yan Y, Chang Y, Ma J. Extraction of polysaccharides from maca enhances the treatment effect of 5-FU by regulating CD4?T cells. Heliyon. 2023;9:e16495. https://doi.org/10.1016/j.heliyon.2023.e16495. [60] Guo T, Yang Y, Gao M, Qu Y, Guo X, Liu Y, et al. Lepidium meyenii Walpers polysaccharide and its cationic derivative re-educate tumor-associated macrophages for synergistic tumor immunotherapy. Carbohydr Polym. 2020;250:116904. https://doi.org/10.1016/j.carbpol.2020.116904. [61] Fei W, Zhang J, Yu S, Yue N, Ye D, Zhu Y, et al. Antioxidative and energy metabolism-improving effects of maca polysaccharide on cyclophosphamide-induced hepatotoxicity mice via metabolomic analysis and Keap1-Nrf2 pathway. Nutrients. 2022;14:4264. https://doi.org/10.3390/nu14204264. [62] Zhang L, Zhao Q, Wang L, Zhao M, Zhao B. Protective effect of polysaccharide from maca (Lepidium meyenii) on Hep-G2 cells and alcoholic liver oxidative injury in mice. Int J Biol Macromol. 2017;99:63–70. https://doi.org/10.1016/j.ijbiomac.2017.01.125. [63] Zhang J, Peng Z, Cheng D, Yao W, Li H, Zhang Q, et al. Lepidium meyenii (maca) polysaccharides mitigate liver toxicity of aflatoxin B? through activation of NRF-2/GPX and AhR/STAT3 signaling pathways. Toxicon. 2024;250:108117. https://doi.org/10.1016/j.toxicon.2024.108117. [64] Chen W, Zhu X, Wang L, Xin X, Zhang M. Effects of two polysaccharides from Lepidium meyenii (maca) on intestinal immunity and inflammation in vitro. Food Funct. 2022. https://doi.org/10.1039/D1FO02659C. [65] Huerta Ojeda á, Rodríguez Rojas J, Cuevas Guí?ez J, Ciriza Velásquez S, Cancino-López J, Barahona-Fuentes G, et al. The effects of maca (Lepidium meyenii Walp) on cellular oxidative stress: a systematic review and meta-analysis. Antioxidants. 2024;13:1046. https://doi.org/10.3390/antiox13091046. [66] Zhou Y, Zhu L, Li H, Xie W, Liu J, Zhang Y, et al. In vivo and in vitro neuroprotective effects of maca polysaccharide. Front Biosci-Landmark. 2022;27:008. https://doi.org/10.31083/j.fbl2701008. [67] Rodríguez-Huamán á, Casimiro-Gonzales S, Chávez-Pérez JA, Gonzales-Arimborgo C, Cisneros-Fernández R, Aguilar-Mendoza L, et al. Antioxidant and neuroprotector effect of Lepidium meyenii (maca) methanol leaf extract against 6-hydroxy dopamine (6-OHDA)-induced toxicity in PC12 cells. Toxicol Mech Methods. 2017;27:279–85. https://doi.org/10.1080/15376516.2016.1275908. [68] Guo SS, Gao XF, Gu YR, Wan ZX, Lu AM, Qin ZH, et al. Preservation of cognitive function by Lepidium meyenii (maca) is associated with improvement of mitochondrial activity and upregulation of autophagy-related proteins in middle-aged mouse cortex. Evid Based Complement Alternat Med. 2016;2016:4394261. https://doi.org/10.1155/2016/4394261. [69] Orhan C, Gencoglu H, Tuzcu M, Sahin N, Ojalvo Sara P, Sylla S, et al. Maca could improve endurance capacity possibly by increasing mitochondrial biogenesis pathways and antioxidant response in exercised rats. J Food Biochem. 2022;46:e14159. https://doi.org/10.1111/jfbc.14159. [70] Murphy E, Fehrenbach G, Zainol I, Buckley C, Montgomery T, Pogue R, et al. Polysaccharides—naturally occurring immune modulators. Polymers. 2023;15:2373. https://doi.org/10.3390/polym15102373. [71] Deng Y, Xie J, Luo Z, Li SP, Zhao J. Synergistic immunomodulatory effect of complex polysaccharides from seven herbs and their major active fractions. Int J Biol Macromol. 2020;165:530–41. https://doi.org/10.1016/j.ijbiomac.2020.09.199. [72] Chen R, Xu J, Wu W, Wen Y, Lu S, El-Seedi HR, et al. Structure–immunomodulatory activity relationships of dietary polysaccharides. Curr Res Food Sci. 2022;5:1330–41. https://doi.org/10.1016/j.crfs.2022.08.016. [73] Li K, Cao Y, Jiao S, Du G, Du Y, Qin X. Structural characterization and immune activity screening of polysaccharides with different molecular weights from Astragali Radix. Front Pharmacol. 2020;11:582091. https://doi.org/10.3389/fphar.2020.582091. [74] Eswar K, Mukherjee S, Ganesan P, Rengan AK. Immunomodulatory natural polysaccharides: an overview of the mechanisms involved. Eur Polym J. 2023;188:111935. https://doi.org/10.1016/j.eurpolymj.2023.111935. [75] Ren L, Zhang J, Zhang T. Immunomodulatory activities of polysaccharides from Ganoderma on immune effector cells. Food Chem. 2021;340:127933. https://doi.org/10.1016/j.foodchem.2020.127933. [76] Yin M, Zhang Y, Li H. Advances in research on immunoregulation of macrophages by plant polysaccharides. Front Immunol. 2019;10:145. https://doi.org/10.3389/fimmu.2019.00145. [77] Guidugli S, Villegas M, Benegas J, Donati I, Paoletti S. Solvation and expansion of neutral and charged chains of a carbohydrate polyelectrolyte: galacturonan in water. A critical revisiting. Biophys Chem. 2023;295:106960. https://doi.org/10.1016/j.bpc.2023.106960. [78] Byeon SE, Lee J, Kim JH, Yang WS, Kwak YS, Kim SY, et al. Molecular mechanism of macrophage activation by red ginseng acidic polysaccharide from Korean red ginseng. Mediators Inflamm. 2012;2012:732860. https://doi.org/10.1155/2012/732860. [79] Wang D, Shao S, Zhang Y, Zhao D, Wang M. Insight into polysaccharides from Panax ginseng C. A. Meyer in improving intestinal inflammation: modulating intestinal microbiota and autophagy. Front Immunol. 2021;12:683911. https://doi.org/10.3389/fimmu.2021.683911. [80] Nystr?m B, Kj?niksen A-L, Beheshti N, Maleki A, Zhu K, Knudsen KD, et al. Characterization of polyelectrolyte features in polysaccharide systems and mucin. Adv Colloid Interface Sci. 2010;158:108–18. https://doi.org/10.1016/j.cis.2009.05.003. [81] Huang L, Zhao J, Wei Y, Yu G, Li F, Li Q. Structural characterization and mechanisms of macrophage immunomodulatory activity of a pectic polysaccharide from Cucurbita moschata Duch. Carbohydr Polym. 2021;269:118288. https://doi.org/10.1016/j.carbpol.2021.118288. [82] Su Y, Chen L, Yang F, Cheung PCK. Beta-D-glucan-based drug delivery system and its potential application in targeting tumor associated macrophages. Carbohydr Polym. 2021;253:117258. https://doi.org/10.1016/j.carbpol.2020.117258. [83] Guo X, Kang J, Xu Z, Guo Q, Zhang L, Ning H, et al. Triple-helix polysaccharides: formation mechanisms and analytical methods. Carbohydr Polym. 2021;262:117962. https://doi.org/10.1016/j.carbpol.2021.117962. [84] Ferwerda G, Meyer-Wentrup F, Kullberg BJ, Netea MG, Adema GJ. Dectin-1 synergizes with TLR2 and TLR4 for cytokine production in human primary monocytes and macrophages. Cell Microbiol. 2008;10:2058–66. https://doi.org/10.1111/j.1462-5822.2008.01188.x. [85] Brown J, O’Callaghan CA, Marshall AS, Gilbert RJ, Siebold C, Gordon S, et al. Structure of the fungal beta-glucan-binding immune receptor dectin-1: implications for function. Protein Sci. 2007;16:1042–52. https://doi.org/10.1110/ps.072791207. [86] Mata-Martínez P, Bergón-Gutiérrez M, del Fresno C. Dectin-1 signaling update: new perspectives for trained immunity. Front Immunol. 2022;13:812148. https://doi.org/10.3389/fimmu.2022.812148. [87] Gantner BN, Simmons RM, Canavera SJ, Akira S, Underhill DM. Collaborative induction of inflammatory responses by dectin-1 and Toll-like receptor 2. J Exp Med. 2003;197:1107–17. https://doi.org/10.1084/jem.20021787. [88] Ferreira SS, Passos CP, Madureira P, Vilanova M, Coimbra MA. Structure–function relationships of immunostimulatory polysaccharides: a review. Carbohydr Polym. 2015;132:378–96. https://doi.org/10.1016/j.carbpol.2015.05.079. [89] Su CH, Lu MK, Lu TJ, Lai MN, Ng LT. A (1→6)-branched (1→4)-β-D-glucan from Grifola frondosa inhibits lipopolysaccharide-induced cytokine production in RAW264.7 macrophages by binding to TLR2 rather than dectin-1 or CR3 receptors. J Nat Prod. 2020;83:231–42. https://doi.org/10.1021/acs.jnatprod.9b00584. [90] Nair PK, Melnick SJ, Ramachandran R, Escalon E, Ramachandran C. Mechanism of macrophage activation by (1,4)-alpha-D-glucan isolated from Tinospora cordifolia. Int Immunopharmacol. 2006;6:1815–24. https://doi.org/10.1016/j.intimp.2006.07.028. [91] Silva-Lagos L, Ijaz A, Buwalda P, Kassai S, Klostermann CE, Leemhuis H, et al. Immunostimulatory effects of isomalto/malto-polysaccharides via TLR2 and TLR4 in preventing doxycycline-induced cytokine loss. Carbohydr Polym. 2025;350:122980. https://doi.org/10.1016/j.carbpol.2024.122980. [92] Lepenies B, Lee J, Sonkaria S. Targeting C-type lectin receptors with multivalent carbohydrate ligands. Adv Drug Deliv Rev. 2013;65:1271–81. https://doi.org/10.1016/j.addr.2013.05.007. [93] Wang Q, Sheng X, Shi A, Hu H, Yang Y, Liu L, et al. β-Glucans: relationships between modification, conformation and functional activities. Molecules. 2017;22:257. https://doi.org/10.3390/molecules22020257. [94] Suzuki T, Kusano K, Kondo N, Nishikawa K, Kuge T, Ohno N. Biological activity of high-purity β-1,3-1,6-glucan derived from the black yeast Aureobasidium pullulans: a literature review. Nutrients. 2021;13:242. https://doi.org/10.3390/nu13010242. [95] Sletmoen M, Naess SN, Stokke BT. Structure and stability of polynucleotide-(1,3)-β-D-glucan complexes. Carbohydr Polym. 2009;76:389–99. https://doi.org/10.1016/j.carbpol.2008.10.035. [96] Du B, Meenu M, Liu H, Xu B. A concise review on the molecular structure and function relationship of β-glucan. Int J Mol Sci. 2019;20:4032. https://doi.org/10.3390/ijms20164032. [97] Ansari E, Alvandi H, Kianirad S, Hatamian-Zarmi A, Mokhtari-Hosseini ZB. Research progress on production and biomedical applications of schizophyllan as a tailor-made polysaccharide: a review. Carbohydr Polym. 2025;348:122770. https://doi.org/10.1016/j.carbpol.2024.122770. [98] Manabe N, Yamaguchi Y. 3D structural insights into β-glucans and their binding proteins. Int J Mol Sci. 2021;22:1578. https://doi.org/10.3390/ijms22041578. [99] Okobira T, Miyoshi K, Uezu K, Sakurai K, Shinkai S. Molecular dynamics studies of side chain effect on the β-1,3-D-glucan triple helix in aqueous solution. Biomacromol. 2008;9:783–8. https://doi.org/10.1021/bm700511d. [100] Vetter J. The mushroom glucans: molecules of high biological and medicinal importance. Foods. 2023;12:1009. https://doi.org/10.3390/foods12051009. [101] Wang X, Zhang Y, Zhang L, Ding Y. Multiple conformation transitions of triple helical lentinan in DMSO/water by microcalorimetry. J Phys Chem B. 2009;113:9915–23. https://doi.org/10.1021/jp811289y. [102] Wu X, Zheng Z, Guo T, Wang K, Zhang Y. Molecular dynamics simulation of lentinan and its interaction with the innate receptor dectin-1. Int J Biol Macromol. 2021;171:527–38. https://doi.org/10.1016/j.ijbiomac.2021.01.032. [103] Xu S, Xu X, Zhang L. Branching structure and chain conformation of water-soluble glucan extracted from Auricularia auricula-judae. J Agric Food Chem. 2012;60:3498–506. https://doi.org/10.1021/jf300423z. [104] Meng Y, Lyu F, Xu X, Zhang L. Recent advances in chain conformation and bioactivities of triple-helix polysaccharides. Biomacromol. 2020;21:1653–77. https://doi.org/10.1021/acs.biomac.9b01644. [105] Zheng Q, Cheng Z, Duan Y, Hu K, Cai M, Zhang H. Effect of subcritical water temperature on the chain conformation and immune activity of ginger polysaccharides. Int J Biol Macromol. 2024;261:129833. https://doi.org/10.1016/j.ijbiomac.2024.129833. |
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