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Chinese Livestock and Poultry Breeding ›› 2026, Vol. 22 ›› Issue (9): 12-25.doi: 10.19543/j.cnki.1673-4556.20260602.003cstr: 32418.14.j.cnki.1673-4556.20260805.001

• Basic Research and Application of Livestock and Poultry Stem Cells •     Next Articles

Advances in early embryonic development and embryo-derived stem cells in livestock

Jinyun He1, Zimo Zhao1, Xiaowei Zhang1, Zhiqiang Feng1, Dengfeng Gao2, Minglei Zhi1()   

  1. 1. College of Biological Sciences, State Key Laboratory of Animal Biotech Breeding, Frontiers Science Center for Molecular Design Breeding, China Agricultural University, Beijing, 100093
    2. College of Animal Science and Technology, Sichuan Agricultural University, Chengdu, 611130, Sichuan
  • Received:2025-12-31 Online:2026-09-26 Published:2026-09-10
  • Contact: Minglei Zhi

Abstract:

Embryo-derived stem cells derived from livestock early embryos possess both self-renewal capacity and multidirectional differentiation potential. The isolation and establishment of embryo-derived stem cell lines essentially represent the capture of the pluripotent state from in vivo embryos and its in vitro maintenance; the dynamic evolution of pluripotency during early embryonic and extraembryonic development in livestock provides a key reference for defining the pluripotent characteristics of embryo-derived stem cells. This review focuses on early embryonic development and embryo-derived stem cell research in livestock such as pigs, cattle, and sheep. It systematically outlines key events including zygotic genome activation, the first and second lineage specification, and gastrulation, and compares the similarities and differences between early embryonic development in livestock and that in humans and mice from perspectives such as developmental timing, signaling pathways, molecular expression, and phenotypic features. On this basis, the review further categorizes embryo-derived stem cells according to their developmental potential, summarizing the latest research progress in livestock from three aspects: expanded pluripotent stem cells, embryonic stem cells, and extra-embryonic stem cells. It systematically compares the differences between these three types of stem cells in terms of isolation stage, cellular and molecular characteristics, key culture systems, and pluripotency and developmental potential, and discusses their application prospects in areas such as embryo and organ development modeling, genetic breeding improvement, and cell-cultured meat production. Furthermore, the review delves into the bottlenecks and challenges faced by research on livestock embryo-derived stem cells, covering precise regulation of pluripotency maintenance and directed differentiation, chimera formation and cross-species applications, improvement of gene editing efficiency and accuracy, stem cell embryo cloning technologies, among others. It also provides an outlook on future research directions, aiming to offer references for studies on livestock embryonic development and stem cells.

Key words: Livestock, Embryonic development, Embryo-derived stem cells

CLC Number: 

  • S81

Fig. 1

Comparative analysis of key developmental events and their timing in livestock(pig,cattle,sheep),mouse and human embryos Note: E, ICM, TE, TB, EPI, PrE, ExE, VE, AC, YS, PS, Meso, and Ecto represent embryonic development days, inner cell mass, trophectoderm, trophoblast, epiblast, primitive endoderm, extraembryonic ectoderm, visceral endoderm, amniotic cavity, yolk sac, primitive streak, mesoderm and ectoderm, respectively. The figure was created using Adobe Illustrator 2024."

Fig. 2

Summary of culture systems for domestic animal embryo-derived stem cells Note: This figure summarizes the basic culture media, feeder layers, basic supplements, cytokines, and small-molecule inhibitors for embryonic stem cells derived from common livestock and poultry such as pigs, cattle, and sheep. EPSC, naïve ESC, formative ESC, primed ESC, XEN, and TSC represent extended pluripotent stem cells, naïve embryonic stem cells, formative embryonic stem cells, primed embryonic stem cells, extraembryonic endoderm stem cells, and trophoblast stem cells, respectively. This figure was created using Adobe Illustrator 2024."

Fig. 3

Application prospects of livestock embryo-derived stem cells Note: The figure was created using Adobe Illustrator 2024."

[1]
HU B J, JIN H, SHI Y, et al. Single-cell RNA-Seq reveals the earliest lineage specification and X chromosome dosage compensation in bovine preimplantation embryos[J]. The FASEB Journal, 2024, 38(4): e23492.
[2]
SCATOLIN G N, MING H, WANG Y J, et al. Single-cell transcriptional landscapes of bovine peri-implantation development[J]. iScience, 2024, 27(4): 109605.
[3]
CAI L, HYUN S H, KIM E. Stem cell factor’s role in enhancing the quality of fertilized and cloned porcine embryos for improved embryonic stem cell derivation[J]. Frontiers in Veterinary Science, 2023, 10: 1285530.
[4]
BOTIGELLI R C, GUILTINAN C, ARCANJO R B, et al. In vitro gametogenesis from embryonic stem cells in livestock species: recent advances, opportunities, and challenges to overcome[J]. Journal of Animal Science, 2023, 101: skad137.
[5]
BAZER F W, JOHNSON G A. Early embryonic development in agriculturally important species[J]. Animals, 2024, 14(13): 1882.
[6]
FRIEDLI M, TRONO D. The developmental control of transposable elements and the evolution of higher species[J]. Annual Review of Cell and Developmental Biology, 2015, 31: 429-451.
[7]
TADROS W, LIPSHITZ H D. The maternal-to-zygotic transition: a play in two acts[J]. Development, 2009, 136(18): 3033-3042.
[8]
DU Z Q, LIANG H, LIU X M, et al. Single cell RNA-seq reveals genes vital to in vitro fertilized embryos and parthenotes in pigs[J]. Scientific Reports, 2021, 11: 14393.
[9]
JUKAM D, SHARIATI S A M, SKOTHEIM J M. Zygotic genome activation in vertebrates[J]. Developmental Cell, 2017, 42(4): 316-332.
[10]
GASSLER J, KOBAYASHI W, GÁSPÁR I, et al. Zygotic genome activation by the totipotency pioneer factor Nr5a2[J]. Science, 2022, 378(6626): 1305-1315.
[11]
MIAO L Y, TANG Y, BONNEAU A R, et al. The landscape of pioneer factor activity reveals the mechanisms of chromatin reprogramming and genome activation[J]. Molecular Cell, 2022, 82(5): 986-1002.e9.
[12]
ZHAI J L, XIAO Z Y, WANG Y M, et al. Human embryonic development: from peri-implantation to gastrulation[J]. Trends in Cell Biology, 2022, 32(1): 18-29.
[13]
ZHI M L, ZHANG J Y, TANG Q Z, et al. Generation and characterization of stable pig pregastrulation epiblast stem cell lines[J]. Cell Research, 2022, 32(4): 383-400.
[14]
KONG Q R, YANG X, ZHANG H, et al. Lineage specification and pluripotency revealed by transcriptome analysis from oocyte to blastocyst in pig[J]. The FASEB Journal, 2020, 34(1): 691-705.
[15]
GIRALDO A M, DECOURCY K, BALL S F, et al. Gene expression of Dnmt1 isoforms in porcine oocytes, embryos, and somatic cells[J]. Cellular Reprogramming, 2013, 15(4): 309-321.
[16]
LU X K, ZHANG Y, WANG L J, et al. Evolutionary epigenomic analyses in mammalian early embryos reveal species-specific innovations and conserved principles of imprinting[J]. Science Advances, 2021, 7(48): eabi6178.
[17]
ZHANG J Y, LI R B, LUO R J, et al. Tracing and capturing the epiblast pluripotency of sheep preimplantation embryos[J]. Advanced Science, 2025, 12(36): e17764.
[18]
CHEN Z Y, DJEKIDEL M N, ZHANG Y. Distinct dynamics and functions of H2AK119ub1 and H3K27me3 in mouse preimplantation embryos[J]. Nature Genetics, 2021, 53(4): 551-563.
[19]
BOROVIAK T, STIRPARO G G, DIETMANN S, et al. Single cell transcriptome analysis of human, marmoset and mouse embryos reveals common and divergent features of preimplan-tation development[J]. Development, 2018, 145(21): dev167833.
[20]
SHA Q Q, WU Y W, JIA M Y, et al. Maternal mRNA clearance is associated with the prevention of precocious transcription and genome instability in mouse early embryos[J]. Science Bulletin, 2026, 71(5): 1003-1007.
[21]
KOROTKEVICH E, NIWAYAMA R, COURTOIS A, et al. The apical domain is required and sufficient for the first lineage segregation in the mouse embryo[J]. Developmental Cell, 2017, 40(3): 235-247.e7.
[22]
ZHI M L, GAO D F, YAO Y X, et al. Elucidation of the pluripotent potential of bovine embryonic lineages facilitates the establishment of formative stem cell lines[J]. Cellular and Molecular Life Sciences, 2024, 81(1): 427.
[23]
NOWOTSCHIN S, SETTY M, KUO Y Y, et al. The emergent landscape of the mouse gut endoderm at single-cell resolution[J]. Nature, 2019, 569(7756): 361-367.
[24]
SAIZ N, WILLIAMS K M, SESHAN V E, et al. Asynchronous fate decisions by single cells collectively ensure consistent lineage composition in the mouse blastocyst[J]. Nature Com-munications, 2016, 7: 13463.
[25]
SIMPSON L, STRANGE A, KLISCH D, et al. A single-cell atlas of pig gastrulation as a resource for comparative embryology[J]. Nature Communications, 2024, 15: 5210.
[26]
RAMOS-IBEAS P, SANG F, ZHU Q F, et al. Pluripotency and X chromosome dynamics revealed in pig pre-gastrulating embryos by single cell analysis[J]. Nature Communications, 2019, 10: 500.
[27]
LIU T B, LI J, YU L Q, et al. Cross-species single-cell transcriptomic analysis reveals pre-gastrulation developmental differences among pigs, monkeys, and humans[J]. Cell Discovery, 2021, 7: 8.
[28]
EVANS M J, KAUFMAN M H. Establishment in culture of pluripotential cells from mouse embryos[J]. Nature, 1981, 292(5819): 154-156.
[29]
MARTIN G R. Isolation of a pluripotent cell line from early mouse embryos cultured in medium conditioned by teratocarcinoma stem cells[J]. Proceedings of the National Aca-demy of Sciences of the United States of America, 1981, 78(12): 7634-7638.
[30]
HANDYSIDE A, HOOPER M L, KAUFMAN M H, et al. Towards the isolation of embryonal stem cell lines from the sheep[J]. Roux’s Archives of Developmental Biology, 1987, 196(3): 185-190.
[31]
NOTARIANNI E, LAURIE S, MOOR R M, et al. Maintenance and differentiation in culture of pluripotential embryonic cell lines from pig blastocysts[J]. Journal of Reproduction and Fertility Supplement, 1990, 41: 51-56.
[32]
STROJEK R M, REED M A, HOOVER J L, et al. A method for cultivating morphologically undifferentiated embryonic stem cells from porcine blastocysts[J]. Theriogenology, 1990, 33(4): 901-913.
[33]
SAITO S, STRELCHENKO N, NIEMANN H. Bovine embryonic stem cell-like cell lines cultured over several passages[J]. Roux’s Archives of Developmental Biology, 1992, 201(3): 134-141.
[34]
NICHOLS J, SMITH A. Naive and primed pluripotent states[J]. Cell Stem Cell, 2009, 4(6): 487-492.
[35]
YANG Y, LIU B, XU J, et al. Derivation of pluripotent stem cells with in vivo embryonic and extraembryonic potency[J]. Cell, 2017, 169(2): 243-257.e25.
[36]
SMITH A. Formative pluripotency: the executive phase in a developmental continuum[J]. Development, 2017, 144(3): 365-373.
[37]
SHEN H, YANG M, LI S Y, et al. Mouse totipotent stem cells captured and maintained through spliceosomal repression[J]. Cell, 2021, 184(11): 2843-2859.e20.
[38]
PENG B, WANG Q Y, ZHANG F X, et al. Mouse totipotent blastomere-like cells model embryogenesis from zygotic genome activation to post implantation[J]. Cell Stem Cell, 2025, 32(3): 391-408.e11.
[39]
YANG J, RYAN D J, WANG W, et al. Establishment of mouse expanded potential stem cells[J]. Nature, 2017, 550(7676): 393-397.
[40]
GAO X F, NOWAK-IMIALEK M, CHEN X, et al. Establishment of porcine and human expanded potential stem cells[J]. Nature Cell Biology, 2019, 21(6): 687-699.
[41]
ZHAO L X, GAO X F, ZHENG Y X, et al. Establishment of bovine expanded potential stem cells[J]. Proceedings of the National Academy of Sciences of the United States of America, 2021, 118(15): e2018505118.
[42]
TAKASHIMA Y, GUO G, LOOS R, et al. Resetting transcription factor control circuitry toward ground-state pluripotency in human[J]. Cell, 2014, 158(6): 1254-1269.
[43]
THEUNISSEN T W, POWELL B E, WANG H Y, et al. Systematic identification of culture conditions for induction and maintenance of naive human pluripotency[J]. Cell Stem Cell, 2014, 15(4): 471-487.
[44]
KINOSHITA M, BARBER M, MANSFIELD W, et al. Capture of mouse and human stem cells with features of formative pluripotency[J]. Cell Stem Cell, 2021, 28(3): 453-471.e8.
[45]
YU L Q, WEI Y L, SUN H X, et al. Derivation of intermediate pluripotent stem cells amenable to primordial germ cell specification[J]. Cell Stem Cell, 2021, 28(3): 550-567.e12.
[46]
KOJIMA Y, KAUFMAN-FRANCIS K, STUDDERT J B, et al. The transcriptional and functional properties of mouse epiblast stem cells resemble the anterior primitive streak[J]. Cell Stem Cell, 2014, 14(1): 107-120.
[47]
ZHANG M L, WANG C Y, JIANG H B, et al. Derivation of novel naive-like porcine embryonic stem cells by a reprogramming factor-assisted strategy[J]. The FASEB Journal, 2019, 33(8): 9350-9361.
[48]
ZHANG X, XUE B H, LI Y, et al. A novel chemically defined serum- and feeder-free medium for undifferentiated growth of porcine pluripotent stem cells[J]. Journal of Cellular Physiology, 2019, 234(9): 15380-15394.
[49]
LI Y, WU S, LI X C, et al. Wnt signaling associated small molecules improve the viability of pPSCs in a PI3K/Akt pathway dependent way[J]. Journal of Cellular Physiology, 2020, 235(7/8): 5811-5822.
[50]
LI C, HAN X J, WANG J, et al. Mixed-lineage leukemia 1 inhibition enhances the differentiation potential of bovine embryonic stem cells by increasing H3K4 mono-methylation at active promoters[J]. International Journal of Molecular Sciences, 2023, 24(15): 11901.
[51]
JIN M H, HUANG S H, ZHOU S W, et al. Efficient derivation of stable sheep embryonic stem cells opens a new avenue for agricultural and biomedical application[J]. Journal of Advanced Research, 2026, 82: 155-169.
[52]
CHEN X, GUO Z, TONG X Y, et al. Derivation of embryonic stem cells across avian species[J]. Nature Biotechnology, 2025: 1-13.
[53]
KINOSHITA M, KOBAYASHI T, PLANELLS B, et al. Pluripotent stem cells related to embryonic disc exhibit common self-renewal requirements in diverse livestock species[J]. Deve-lopment, 2021, 148(23): dev199901.
[54]
YANG L, DI A Q, SONG L S, et al. Generation of modified cows and sheep from spermatid-like haploid embryonic stem cells[J]. Nature Biotechnology, 2025: 1-9.
[55]
LUO Q, PUI H P, CHEN J Y, et al. Epiblast-like stem cells established by Wnt/β-catenin signaling manifest distinct features of formative pluripotency and germline competence[J]. Cell Reports, 2023, 42(1): 112021.
[56]
CHOI K H, LEE D K, KIM S W, et al. Chemically defined media can maintain pig pluripotency network in vitro [J]. Stem Cell Reports, 2019, 13(1): 221-234.
[57]
BOGLIOTTI Y S, WU J, VILARINO M, et al. Efficient derivation of stable primed pluripotent embryonic stem cells from bovine blastocysts[J]. Proceedings of the National Academy of Sciences of the United States of America, 2018, 115(9): 2090-2095.
[58]
OKAE H, TOH H, SATO T, et al. Derivation of human trophoblast stem cells[J]. Cell Stem Cell, 2018, 22(1): 50-63.e6.
[59]
PARK C H, JEOUNG Y H, UH K J, et al. Extraembryonic endoderm (XEN) cells capable of contributing to embryonic chimeras established from pig embryos[J]. Stem Cell Reports, 2021, 16(1): 212-223.
[60]
WANG Y J, MING H, YU L Q, et al. Establishment of bovine trophoblast stem cells[J]. Cell Reports, 2023, 42(5): 112439.
[61]
PINZÓN-ARTEAGA C A, WANG Y J, WEI Y L, et al. Bovine blastocyst-like structures derived from stem cell cultures[J]. Cell Stem Cell, 2023, 30(5): 611-616.e7.
[62]
SUASNAVAS E A, HEYWOOD S, WARD A, et al. Isolation and characterization of trophoblast-derived stem-like cells from peri-implantation porcine embryos[J]. Animal Reproduction Science, 2015, 154: 128-141.
[63]
KIM E, CAI L, CHOI H, et al. Distinct properties of putative trophoblast stem cells established from somatic cell nuclear-transferred pig blastocysts[J]. Biological Research, 2024, 57(1): 35.
[64]
ZHANG M L, JIN Y, ZHAO L H, et al. Derivation of porcine extra-embryonic endoderm cell lines reveals distinct signaling pathway and multipotency states[J]. International Journal of Molecular Sciences, 2021, 22(23): 12918.
[65]
MING H, SCATOLIN G N, OJEDA-ROJAS O A, et al. Establishment of bovine extraembryonic endoderm stem cells enables efficient blastoid formation[J]. Cell Reports, 2025, 44(6): 115707.
[66]
SMITH M K, CLARK C C, MCCOSKI S R. Technical note: improving the efficiency of generating bovine extraembryonic endoderm cells[J]. Journal of Animal Science, 2020, 98(7): skaa222.
[67]
WANG H N, ZHONG L, WANG Z F, et al. Wnt inhibition safeguards porcine embryonic stem cells from the acquisition of extraembryonic endoderm cell fates[J]. Advanced Science, 2025, 12(17): 2416802.
[68]
VIUKOV S, SHANI T, BAYERL J, et al. Human primed and naïve PSCs are both able to differentiate into trophoblast stem cells[J]. Stem Cell Reports, 2022, 17(11): 2484-2500.
[69]
XU S, WANG S D, TAM T T K K, et al. Derivation of trophoblast stem cells from human expanded potential stem cells[J]. STAR Protocols, 2023, 4(2): 102354.
[70]
XIANG J Z, WANG H N, SHI B B, et al. Pig blastocyst-like structure models from embryonic stem cells[J]. Cell Discovery, 2024, 10: 72.
[71]
MALIK H N, SINGHAL D K, SAINI S, et al. Derivation of oocyte-like cells from putative embryonic stem cells and parthenogenetically activated into blastocysts in goat[J]. Scientific Reports, 2020, 10: 10086.
[72]
RAWAT H, KORNHERR J, ZAWADA D, et al. Recapitulating porcine cardiac development in vitro: from expanded potential stem cell to embryo culture models[J]. Frontiers in Cell and Developmental Biology, 2023, 11: 1111684.
[73]
SHIUE Y L, YANG J R, LIAO Y J, et al. Derivation of porcine pluripotent stem cells for biomedical research[J]. Theriogenology, 2016, 86(1): 176-181.
[74]
LI M S, GUO X Y, CHENG L X, et al. Porcine kidney organoids derived from Naïve-like embryonic stem cells[J]. International Journal of Molecular Sciences, 2024, 25(1): 682.
[75]
HOU Z C, AN L, HAN J Y, et al. Revolutionize livestock breeding in the future: an animal embryo-stem cell breeding system in a dish[J]. Journal of Animal Science and Biotechnology, 2018, 9(1): 90.
[76]
ZHOU X Y, GAO C, ZHAO W X, et al. Advances in the study of pluripotent stem cells in livestock[J]. Cell Proliferation, 2025, 58(8): e70008.
[77]
ZHU G X, GAO D F, LI L Z, et al. Generation of three-dimensional meat-like tissue from stable pig epiblast stem cells[J]. Nature Communications, 2023, 14: 8163.
[78]
YAO Y, ZHU G, ZHI M, et al. Generation of multitissue cell-cultivated meat via multidirectional differentiation of stable porcine epiblast stem cells [J]. Nature communications, 2026, 17(1).
[79]
ZEHORAI E, MAOR-SHOSHANI A, MOLOTSKI N, et al. From fertilised oocyte to cultivated meat - harnessing bovine embryonic stem cells in the cultivated meat industry[J]. Reproduction, Fertility, and Development, 2023, 36(2): 124-132.
[80]
JARA T C, PARK K, VAHMANI P, et al. Stem cell-based strategies and challenges for production of cultivated meat[J]. Nature Food, 2023, 4(10): 841-853.
[81]
KIM S, BEIER A, SCHREYER H B, et al. Environmental life cycle assessment of a novel cultivated meat burger patty in the United States[J]. Sustainability, 2022, 14(23): 16133.
[82]
RODRÍGUEZ ESCOBAR M I, CADENA E, NHU T T, et al. Analysis of the cultured meat production system in function of its environmental footprint: current status, gaps and recommendations[J]. Foods, 2021, 10(12): 2941.
[83]
WANG D S, VILLENAVE R, STOKAR-REGENSCHEIT N, et al. Human organoids as 3D in vitro platforms for drug discovery: opportunities and challenges[J]. Nature Reviews Drug Dis-covery, 2026, 25(3): 204-226.
[84]
DE LAU W B M, WIJNAKKER J J A P M, VAN SON G J F, et al. A single-chain derivative of an integrin-activating antibody potentiates organoid growth in Matrigel and collagen hydrogels[J]. Nature Biotechnology, 2025: 1-11.
[85]
POSFAI E, SCHELL J P, JANISZEWSKI A, et al. Evaluating totipotency using criteria of increasing stringency[J]. Nature Cell Biology, 2021, 23(1): 49-60.
[86]
ALFEGHALY C, ROUGEULLE C. X chromosome inactivation in mammals: general principles and species-specific consi-derations[J]. EMBO Reports, 2025, 26(14): 3478-3490.
[87]
MORATA TARIFA C, LÓPEZ NAVAS L, AZKONA G, et al. Chimeras for the twenty-first century[J]. Critical Reviews in Biotechnology, 2020, 40(3): 283-291.
[88]
LI Y M, SUN S Y, XU Y T, et al. Efficient somatic cell nuclear transfer by overcoming both pre- and post-implantation epigenetic barriers[J]. Advanced Science, 2025, 12(37): e04669.
[89]
KOMOR A C, KIM Y B, PACKER M S, et al. Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage[J]. Nature, 2016, 533(7603): 420-424.
[90]
ANZALONE A V, RANDOLPH P B, DAVIS J R, et al. Search-and-replace genome editing without double-strand breaks or donor DNA[J]. Nature, 2019, 576(7785): 149-157.
[91]
NIU D, WEI H J, LIN L, et al. Inactivation of porcine endogenous retrovirus in pigs using CRISPR-Cas9[J]. Science, 2017, 357(6357): 1303-1307.
[92]
PHILLIPS K G, ALJABBAN I, WOLBROM D H, et al. Cardiac xenotransplantation: current state and future directions[J]. Circulation, 2025, 152(1): 58-73.
[93]
GAO R, WANG C F, GAO Y W, et al. Inhibition of aberrant DNA re-methylation improves post-implantation development of somatic cell nuclear transfer embryos[J]. Cell Stem Cell, 2018, 23(3): 426-435.e5.
[94]
LIU X, WANG Y Z, GAO Y P, et al. H3K9 demethylase KDM4E is an epigenetic regulator for bovine embryonic development and a defective factor for nuclear reprogramming[J]. Development, 2018, 145(4): dev158261.
[95]
GAO Y, WU F F, TANG D D, et al. H3K9me3 and H3K27me3 are epigenetic barriers to somatic cell nuclear transfer in rabbits[J]. American Journal of Translational Research, 2025, 17(4): 3094-3108.
[96]
ZHANG X L, GAO S R, LIU X Y. Advance in the role of epigenetic reprogramming in somatic cell nuclear transfer-mediated embryonic development[J]. Stem Cells International, 2021, 2021: 6681337.
[97]
MOURA M T. Cloning by SCNT: integrating technical and biology-driven advances[J]. Methods in Molecular Biology, 2023, 2647: 1-35.
[98]
ZHOU K, WANG T T, ZHANG J J, et al. LEUTX regulates porcine embryonic genome activation in somatic cell nuclear transfer embryos[J]. Cell Reports, 2024, 43(6): 114372.
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