猪颗粒细胞在卵泡闭锁中的作用机制研究进展

doi:10.11843/j.issn.0366-6964.2025.06.002

摘要/Abstract

摘要：

尽管我国畜牧业已取得了显著进步，但提升畜禽繁殖力仍然是畜牧场不懈追求的目标。卵泡闭锁是未发生排卵的卵泡，这在畜禽中极为普遍，以成为制约畜禽繁殖能力的重要因素，日益受到广泛关注。颗粒细胞作为影响卵泡闭锁的关键因素，在卵泡闭锁过程中发挥了关键的作用，目前，大多研究发现颗粒细胞的增殖可影响卵泡的发育，而颗粒细胞的凋亡会导致卵泡的闭锁，但其背后的潜在机制仍有待深入探究。本文探讨了颗粒细胞在凋亡、自噬、铁死亡、焦亡以及坏死性凋亡等多个方面的作用，为揭示卵泡闭锁的复杂机制提供新的视角和思路。

关键词: 猪, 颗粒细胞, 卵泡闭锁, 凋亡, 自噬, 非编码RNA

Abstract:

Despite the significant advancements in China's animal husbandry sector, enhancing the reproductive capacity of livestock and poultry still remains a relentless pursuit for breeding farms. Follicular atresia, which refers to the non-ovulatory follicles, is extremely common in livestock and poultry and has become a significant factor constraining their reproductive capabilities, thus attracting increasing attention. Granulosa cells, as a key factor affecting follicular atresia, play a crucial role in the process of follicular atresia. Currently, most research findings indicate that the proliferation of granulosa cells can influence the development of follicles, while apoptosis of granulosa cells can lead to follicular atresia. However, the underlying mechanisms still require further exploration. This paper discusses the roles of granulosa cells in apoptosis, autophagy, ferroptosis, pyroptosis, and necroptosis, providing new perspectives and insights into the complex mechanisms of follicular atresia.

Key words: pig, granulosa cells, follicular atresia, apoptosis, autophagy, non-coding RNA

中图分类号:

S828.3

赵顺然, 付桂鑫, 庞钊琪, 夏威, 李俊杰, 陶晨雨. 猪颗粒细胞在卵泡闭锁中的作用机制研究进展[J]. 畜牧兽医学报, 2025, 56(6): 2537-2545.

ZHAO Shunran, FU Guixin, PANG Zhaoqi, XIA Wei, LI Junjie, TAO Chenyu. Research Progress on the Mechanism of Porcine Granulosa Cells in Follicular Atresia[J]. Acta Veterinaria et Zootechnica Sinica, 2025, 56(6): 2537-2545.

图/表 2

表 1

图 1

参考文献 71

1	郭亚军, 柳苗苗, 付德海, 等. 藏绵羊卵巢组织学及卵泡超微形态的观察[J]. 畜牧兽医学报, 2021, 52 (2): 389- 398. doi: 10.11843/j.issn.0366-6964.2021.02.011
	GUO Y J , LIU M M , FU D H , et al. Observation of ovary histology and ultrastructure of follicles in Tibetan sheep[J]. Acta Veterinaria et Zootechnica Sinica, 2021, 52 (2): 389- 398. doi: 10.11843/j.issn.0366-6964.2021.02.011
2	MARCOZZI S , ROSSI V , SALUSTRI A , et al. Programmed cell death in the human ovary[J]. Minerva Ginecol, 2018, 70 (5): 549- 560.
3	梁学超, 蒋明, 罗玉茹, 等. 猪卵巢发育的组织学变化及卵泡闭锁规律研究[J]. 畜牧兽医学报, 2017, 48 (10): 1863- 1870. doi: 10.11843/j.issn.0366-6964.2017.10.009
	LIANG X C , JIANG M , LUO Y R , et al. Study on histology and patterns of follicular atresia during ovarian development in pig[J]. Acta Veterinaria et Zootechnica Sinica, 2017, 48 (10): 1863- 1870. doi: 10.11843/j.issn.0366-6964.2017.10.009
4	DONG M , OUYANG Y , GAO S , et al. Protein phosphatase 4 maintains the survival of primordial follicles by regulating autophagy in oocytes[J]. Cell Death Dis, 2024, 15 (9): 658. doi: 10.1038/s41419-024-07051-4
5	ZHANG X , TAO Q , SHANG J , et al. miR-26a promotes apoptosis of porcine granulosa cells by targeting the 3beta-hydroxysteroid-Delta24-reductase gene[J]. Asian-Australas J Anim Sci, 2020, 33 (4): 547- 555. doi: 10.5713/ajas.19.0173
6	YANG F , CHEN Y , LIU Q , et al. Dynamics and regulations of BimEL Ser65 and Thr112 phosphorylation in porcine granulosa cells during follicular atresia[J]. Cells, 2020, 9 (2): 402. doi: 10.3390/cells9020402
7	LIU J , NING C , ZHANG J , et al. Comparative miRNA expression profile analysis of porcine ovarian follicles: new insights into the initiation mechanism of follicular atresia[J]. Front Genet, 2023, 14, 1338411. doi: 10.3389/fgene.2023.1338411
8	LI Z , RUAN Z , FENG Y , et al. METTL3-mediated m6A methylation regulates granulosa cells autophagy during follicular atresia in pig ovaries[J]. Theriogenology, 2023, 201, 83- 94. doi: 10.1016/j.theriogenology.2023.02.021
9	PAN Y , GAN M , WU S , et al. tRF-Gly-GCC in atretic follicles promotes ferroptosis in granulosa cells by down-regulating MAPK1[J]. Int J Mol Sci, 2024, 25 (16): 9061. doi: 10.3390/ijms25169061
10	GAO X , ZHANG J , PAN Z , et al. The distribution and expression of vascular endothelial growth factor A (VEGFA) during follicular development and atresia in the pig[J]. Reprod Fertil Dev, 2020, 32 (3): 259- 266. doi: 10.1071/RD18508
11	GRZESIAK M , SOCHA M , HRABIA A . Altered vitamin D metabolic system in follicular cysts of sows[J]. Reprod Domest Anim, 2021, 56 (1): 193- 196. doi: 10.1111/rda.13867
12	CAO R , WU W J , ZHOU X L , et al. Expression and preliminary functional profiling of the let-7 family during porcine ovary follicle atresia[J]. Mol Cells, 2015, 38 (4): 304- 311. doi: 10.14348/molcells.2015.2122
13	程颖, 魏全伟, 王喆, 等. 母猪健康和闭锁卵巢有腔卵泡的转录组测序比较分析[J]. 南京农业大学学报, 2023, 46 (3): 555- 563.
	CHENG Y , WEI Q W , WANG Z , et al. Transcriptome sequencing analysis of porcine granulosa cells in healthy and atretic follicles[J]. Journal of Nanjing Agricultural University, 2023, 46 (3): 555- 563.
14	ZHANG J , QIN X , WANG C , et al. Comparative transcriptome profile analysis of granulosa cells from porcine ovarian follicles during early atresia[J]. Anim Biotechnol, 2024, 35 (1): 2282090. doi: 10.1080/10495398.2023.2282090
15	MO J , SUN L , CHENG J , et al. Non-targeted metabolomics reveals metabolic characteristics of porcine atretic follicles[J]. Front Vet Sci, 2021, 8, 679947. doi: 10.3389/fvets.2021.679947
16	ELMORE S . Apoptosis: a review of programmed cell death[J]. Toxicol Pathol, 2007, 35 (4): 495- 516. doi: 10.1080/01926230701320337
17	FUCHS Y , STELLER H . Live to die another way: modes of programmed cell death and the signals emanating from dying cells[J]. Nat Rev Mol Cell Biol, 2015, 16 (6): 329- 344. doi: 10.1038/nrm3999
18	HAGAN M L , MANDER S , JOSEPH C , et al. Upregulation of the EGFR/MEK1/MAPK1/2 signaling axis as a mechanism of resistance to antiestrogen-induced BimEL dependent apoptosis in ER⁺ breast cancer cells[J]. Int J Oncol, 2023, 62 (2): 20.
19	WANG Y , ZENG S . Melatonin promotes ubiquitination of phosphorylated pro-apoptotic protein Bcl-2-interacting mediator of cell death-extra long (Bim(EL)) in porcine granulosa cells[J]. Int J Mol Sci, 2018, 19 (11): 3431. doi: 10.3390/ijms19113431
20	REITER R J , MAYO J C , TAN D , et al. Melatonin as an antioxidant: under promises but over delivers[J]. J Pineal Res, 2016, 61 (3): 253- 278. doi: 10.1111/jpi.12360
21	ZHUO Y , CAO M , GONG Y , et al. Gut microbial metabolism of dietary fibre protects against high energy feeding induced ovarian follicular atresia in a pig model[J]. Bri J Nutr, 2021, 125 (1): 38- 49. doi: 10.1017/S0007114520002378
22	MELINCOVICI C S , BOSCA A B , SUSMAN S , et al. Vascular endothelial growth factor (VEGF)-key factor in normal and pathological angiogenesis[J]. Rom J Morphol Embryol, 2018, 59 (2): 455- 467.
23	DAI W , YANG H , XU B , et al. Human umbilical cord-derived mesenchymal stem cells (hUC-MSCs) alleviate excessive autophagy of ovarian granular cells through VEGFA/PI3K/AKT/mTOR pathway in premature ovarian failure rat model[J]. J Ovarian Res, 2023, 16 (1): 198. doi: 10.1186/s13048-023-01278-z
24	ZHAO Y , WANG J , QIN W , et al. Dehydroepiandrosterone promotes ovarian angiogenesis and improves ovarian function in a rat model of premature ovarian insufficiency by up-regulating HIF-1alpha/VEGF signalling[J]. Reprod Biomed Online, 2024, 49 (3): 103914. doi: 10.1016/j.rbmo.2024.103914
25	SHIMIZU T , JIANG J , SASADA H , et al. Changes of messenger RNA expression of angiogenic factors and related receptors during follicular development in gilts[J]. Biol Reprod, 2002, 67 (6): 1846- 1852. doi: 10.1095/biolreprod.102.006734
26	MA M , ZHANG J , GAO X , et al. miR-361-5p mediates SMAD4 to promote porcine granulosa cell apoptosis through VEGFA[J]. Biomolecules, 2020, 10 (9): 1281. doi: 10.3390/biom10091281
27	MATTICK J S , MAKUNIN I V . Non-coding RNA[J]. Hum Mol Genet, 2006, 15 Spec No 1, R17- R29.
28	DAI L , TSAI-MORRIS C , SATO H , et al. Testis-specific miRNA-469 up-regulated in gonadotropin-regulated testicular RNA helicase (GRTH/DDX25)-null mice silences transition protein 2 and protamine 2 messages at sites within coding region: implications of its role in germ cell development[J]. J Biol Chem, 2011, 286 (52): 44306- 44318. doi: 10.1074/jbc.M111.282756
29	WANG S , WANG Y , CHEN Y , et al. MEIS1 is a common transcription repressor of the miR-23a and NORHA axis in granulosa cells[J]. Int J Mol Sci, 2023, 24 (4): 3589. doi: 10.3390/ijms24043589
30	LIU S , CHEN J , LIU M , et al. miR-107 suppresses porcine granulosa cell proliferation and estradiol synthesis while promoting apoptosis via targeting PTGS2[J]. Theriogenology, 2025, 238, 117367. doi: 10.1016/j.theriogenology.2025.117367
31	NEUNZIG J , BERNHARDT R . Effect of sulfonated steroids on steroidogenic cytochrome P450-dependent steroid hydroxylases[J]. J Steroid Biochem Mol Biol, 2018, 179, 3- 7. doi: 10.1016/j.jsbmb.2017.07.004
32	WANG M , RAMIREZ J , HAN J , et al. The steroidogenic enzyme Cyp11a1 is essential for development of peanut-induced intestinal anaphylaxis[J]. J Allergy Clin Immunol, 2013, 132 (5): 1174- 1183. doi: 10.1016/j.jaci.2013.05.027
33	TIAN J , QIN P , XU T , et al. Chaigui granule exerts anti-depressant effects by regulating the synthesis of Estradiol and the downstream of CYP19A1-E2-ERKs signaling pathway in CUMS-induced depressed rats[J]. Front Pharmacol, 2022, 13, 1005438. doi: 10.3389/fphar.2022.1005438
34	LI Q , DU X , LIU L , et al. Upregulation of miR-146b promotes porcine ovarian granulosa cell apoptosis by attenuating CYP19A1[J]. Domest Anim Endocrinol, 2021, 74, 106509. doi: 10.1016/j.domaniend.2020.106509
35	WANG M , WANG Y , YAO W , et al. lnc2300 is a cis-acting long noncoding RNA of CYP11A1 in ovarian granulosa cells[J]. J Cell Physiol, 2022, 237 (11): 4238- 4250. doi: 10.1002/jcp.30872
36	LI X , YANG L , CHEN L . The biogenesis, functions, and challenges of circular RNAs[J]. Mol Cell, 2018, 71 (3): 428- 442. doi: 10.1016/j.molcel.2018.06.034
37	FU Y , JIANG H , LIU J , et al. Genome-wide analysis of circular RNAs in bovine cumulus cells treated with BMP15 and GDF9[J]. Sci Rep, 2018, 8 (1): 7944. doi: 10.1038/s41598-018-26157-2
38	MENG L , TEERDS K , TAO J , et al. Characteristics of circular RNA expression profiles of porcine granulosa cells in healthy and atretic antral follicles[J]. Int J Mol Sci, 2020, 21 (15): 5217. doi: 10.3390/ijms21155217
39	GUO T Y , HUANG L , YAO W , et al. The potential biological functions of circular RNAs during the initiation of atresia in pig follicles[J]. Domest Anim Endocrinol, 2020, 72, 106401. doi: 10.1016/j.domaniend.2019.106401
40	WANG H , ZHANG Y , ZHANG J , et al. circSLC41A1 resists porcine granulosa cell apoptosis and follicular atresia by promoting SRSF1 through miR-9820-5p sponging[J]. Int J Mol Sci, 2022, 23 (3): 1509. doi: 10.3390/ijms23031509
41	MA M , WANG H , ZHANG Y , et al. circRNA-mediated inhibin-activin balance regulation in ovarian granulosa cell apoptosis and follicular atresia[J]. Int J Mol Sci, 2021, 22 (17): 9113. doi: 10.3390/ijms22179113
42	王彩霞, 秦鑫鑫, 李文洁, 等. 猪卵巢颗粒细胞中circINHBA的鉴定及与细胞凋亡的相关性分析[J]. 畜牧与兽医, 2024, 56 (10): 14- 20.
	WANG C X , QIN X X , LI W J , et al. Identification of circINHBA and its effect on follicular granulosa cell apoptosis in pigs[J]. Animal Husbandry and Veterinary Medicine, 2024, 56 (10): 14- 20.
43	KOPP F , MENDELL J T . Functional classification and experimental dissection of long noncoding RNAs[J]. Cell, 2018, 172 (3): 393- 407. doi: 10.1016/j.cell.2018.01.011
44	MENG L , ZHAO K , WANG C C , et al. Characterization of long non-coding RNA profiles in porcine granulosa cells of healthy and atretic antral follicles: Implications for a potential role in apoptosis[J]. Int J Mol Sci, 2021, 22 (5): 2677. doi: 10.3390/ijms22052677
45	WANG M , WANG Y , YANG L , et al. Nuclear lncRNA NORSF reduces E2 release in granulosa cells by sponging the endogenous small activating RNA miR-339[J]. BMC Biol, 2023, 21 (1): 221. doi: 10.1186/s12915-023-01731-x
46	WANG M , SHENG W , ZHANG J , et al. A mutation losing an RBP-binding site in the lncRNA NORSF transcript influences granulosa cell apoptosis and sow fertility[J]. Adv Sci (Weinh), 2024, 11 (40): e2404747. doi: 10.1002/advs.202404747
47	DU X , LIU L , LI Q , et al. NORFA, long intergenic noncoding RNA, maintains sow fertility by inhibiting granulosa cell death[J]. Commun Biol, 2020, 3 (1): 131. doi: 10.1038/s42003-020-0864-x
48	DU X , LI Q , YANG L , et al. Transcriptomic data analyses reveal that sow fertility-related lincRNA NORFA is essential for the normal states and functions of granulosa cells[J]. Front Cell Dev Biol, 2021, 9, 610553. doi: 10.3389/fcell.2021.610553
49	GUO Z , ZENG Q , LI Q , et al. LncRNA NORFA promotes the synthesis of estradiol and inhibits the apoptosis of sow ovarian granulosa cells through SF-1/CYP11A1 axis[J]. Biol Direct, 2024, 19 (1): 107. doi: 10.1186/s13062-024-00563-1
50	LOOS B , ENGELBRECHT A , LOCKSHIN R A , et al. The variability of autophagy and cell death susceptibility: Unanswered questions[J]. Autophagy, 2013, 9 (9): 1270- 1285. doi: 10.4161/auto.25560
51	MENG L , JAN S Z , HAMER G , et al. Preantral follicular atresia occurs mainly through autophagy, while antral follicles degenerate mostly through apoptosis[J]. Biol Reprod, 2018, 99 (4): 853- 863.
52	ZHENG Y , MA L , LIU N , et al. Autophagy and apoptosis of porcine ovarian granulosa cells during follicular development[J]. Animals (Basel), 2019, 9 (12): 1111.
53	GIOIA L , FESTUCCIA C , COLAPIETRO A , et al. Abundances of autophagy-related protein LC3B in granulosa cells, cumulus cells, and oocytes during atresia of pig antral follicles[J]. Anim Reprod Sci, 2019, 211, 106225. doi: 10.1016/j.anireprosci.2019.106225
54	CAO M , CHEN X , WANG Y , et al. The reduction of the m⁶A methyltransferase METTL3 in granulosa cells is related to the follicular cysts in pigs[J]. J Cell Physiol, 2024, 239 (6): e31289. doi: 10.1002/jcp.31289
55	LIU G , WANG Y , ZHENG Y , et al. PHB2 binds to ERbeta to induce the autophagy of porcine ovarian granulosa cells through mTOR phosphorylation[J]. Theriogenology, 2023, 198, 114- 122. doi: 10.1016/j.theriogenology.2022.12.031
56	ZHANG X , LI M , HUANG M , et al. Effect of RFRP-3, the mammalian ortholog of GnIH, on apoptosis and autophagy in porcine ovarian granulosa cells via the p38MAPK pathway[J]. Theriogenology, 2022, 180, 137- 145. doi: 10.1016/j.theriogenology.2021.12.024
57	WANG S , YAO Q , ZHAO F , et al. 1α, 25(OH)₂ D₃ promotes the autophagy of porcine ovarian granulosa cells as a protective mechanism against ROS through the BNIP3/PINK1 pathway[J]. Int J Mol Sci, 2023, 24 (5): 4364. doi: 10.3390/ijms24054364
58	XING W , WANG B , LI M , et al. The dual role of ATG7: Regulation of autophagy and apoptosis in porcine ovarian follicular granulosa cells[J]. Anim Reprod Sci, 2024, 270, 107601. doi: 10.1016/j.anireprosci.2024.107601
59	GAO W , WANG X , ZHOU Y , et al. Autophagy, ferroptosis, pyroptosis, and necroptosis in tumor immunotherapy[J]. Signal Transduct Target Ther, 2022, 7 (1): 196. doi: 10.1038/s41392-022-01046-3
60	WU X , LI Y , ZHANG S , et al. Ferroptosis as a novel therapeutic target for cardiovascular disease[J]. Theranostics, 2021, 11 (7): 3052- 3059. doi: 10.7150/thno.54113
61	WANG D , WAN X . Progress in the study of molecular mechanisms of cell pyroptosis in tumor therapy[J]. Int Immunopharmacol, 2023, 118, 110143. doi: 10.1016/j.intimp.2023.110143
62	WU H , HAN Y , LIU J , et al. The assembly and activation of the PANoptosome promote porcine granulosa cell programmed cell death during follicular atresia[J]. J Anim Sci Biotechnol, 2024, 15 (1): 147. doi: 10.1186/s40104-024-01107-3
63	MENG L , WU Z , ZHAO K , et al. Transcriptome analysis of porcine granulosa cells in healthy and atretic follicles: Role of steroidogenesis and oxidative stress[J]. Antioxidants (Basel), 2020, 10 (1): 22. doi: 10.3390/antiox10010022
64	LIU S , JIA Y , MENG S , et al. Mechanisms of and potential medications for oxidative stress in ovarian granulosa cells: A review[J]. Int J Mol Sci, 2023, 24 (11): 9205. doi: 10.3390/ijms24119205
65	KONG C , SU J , WANG Q , et al. Signaling pathways of Periplaneta americana peptide resist H₂O₂-induced apoptosis in pig-ovary granulosa cells through FoxO1[J]. Theriogenology, 2022, 183, 108- 119. doi: 10.1016/j.theriogenology.2022.02.004
66	ZHANG J , REN Q , CHEN J , et al. Autophagy contributes to oxidative stress-induced apoptosis in porcine granulosa cells[J]. Reprod Sci, 2021, 28 (8): 2147- 2160.
67	SHEN L , LIU J , LUO A , et al. The stromal microenvironment and ovarian aging: mechanisms and therapeutic opportunities[J]. J Ovarian Res, 2023, 16 (1): 237.
68	LI C , ZHOU J , LIU Z , et al. FSH prevents porcine granulosa cells from hypoxia-induced apoptosis via activating mitophagy through the HIF-1alpha-PINK1-Parkin pathway[J]. FASEB J, 2020, 34 (3): 3631- 3645.
69	ZHANG X , CHEN Y , LI H , et al. Sulforaphane acts through NFE2L2 to prevent hypoxia-induced apoptosis in porcine granulosa cells via activating antioxidant defenses and mitophagy[J]. J Agric Food Chem, 2022, 70 (26): 8097- 8110.
70	LIU Z , LI C , WU G , et al. Involvement of JNK/FOXO1 pathway in apoptosis induced by severe hypoxia in porcine granulosa cells[J]. Theriogenology, 2020, 154, 120- 127.
71	TAO J , ZHANG X , ZHOU J , et al. Melatonin alleviates hypoxia-induced apoptosis of granulosa cells by reducing ROS and activating MTNR1B-PKA-Caspase8/9 pathway[J]. Antioxidants (Basel), 2021, 10 (2): 184.

基因/蛋白/非编码RNA Gene/protein/noncoding RNA	作用机制 Mechanism of action	类型 Type	参考文献 references
BIMEL	氧化应激激活JNK上调p-BimEL-T112水平促进GC细胞凋亡	凋亡	Yang等^[6]
VEGFA	miR-361-5p抑制VEGFA基因3′UTR促进GC细胞凋亡	凋亡	Ma等^[26]
miR-23a	miR-23a受到MEIS1的调节，控制FOXO1的表达促进细胞凋亡	凋亡	Wang等^[29]
miR-146b	miR-146b抑制CYP19A1表达	激素	Li等^[34]
miR-365-3p	miR-365-3p促进GC凋亡并可以调控CYP11A1表达	凋亡、激素	Wang等^[35]
circSLC41A1	circSLC41A1与miR-9820-5p结合下调SRSF1表达，促进GC凋亡	凋亡	Guo等^[39]
circINHA-001	circINHA-001与miR-214-5p、miR-7144-3p miR-9830-5p结合下调INHBA表达，增加抑制素表达，促进GC凋亡	凋亡	Ma等^[41]
lncRNA-NORSF	lncRNA-NORSF通过调控miR-339降低CYP19A1表达，并与miR-126相互作用，抑制TGFBR2表达，促进GC凋亡	凋亡、激素	Wang等^[45-46]
ULK1	ULK1的m⁶A修饰降低而增加其表达，促进自噬发生	自噬	Li等^[8]
tRF-1:30-Gly-GCC-2	tRF-1:30-Gly-GCC-2通过抑制MAPK1信号通路抑制颗粒细胞增殖并促进铁死亡	铁死亡	Pan等^[9]
ZBP1、RIPK3和RIPK1	ZBP1、RIPK3和RIPK1组成的PANoptosome复合物导致闭锁卵泡GC的坏死性凋亡与焦亡是	坏死性凋亡、焦亡	Wu等^[62]

[1]	王运珂, 王娜, 岳珂, 何坤淼, 张兴, 刘垚, 张改平. 体外对猪流行性腹泻病毒复制具有抑制效应的物质[J]. 畜牧兽医学报, 2025, 56(6): 2577-2589.
[2]	吴超, 明文含, 卢姝婉, 杨彩梅, 刘金松, 马翔, 张瑞强. 猪流行性腹泻病毒的天然免疫逃避机制及其防控研究进展[J]. 畜牧兽医学报, 2025, 56(6): 2590-2599.
[3]	周敏, 汤德元, 曾智勇, 王彬, 黄涛, 胡雯雯, 毛茵茗, 周飘, 何松. 猪流行性腹泻病毒蛋白与宿主蛋白相互作用的研究进展[J]. 畜牧兽医学报, 2025, 56(6): 2600-2612.
[4]	吴桐, 王楠, 邢雨欣, 张犇, 胡潘阳, 张海涛, 朱玉峰, 吴相哲, 杨峰, 李秀领, 王克君, 韩雪蕾, 李新建, 余彤, 柏峻, 李改英, 乔瑞敏. 豫南黑猪背膘厚度与全基因组拷贝数变异的关联研究[J]. 畜牧兽医学报, 2025, 56(6): 2639-2648.
[5]	柳思奇, 杨榛, 杨雅楠, 蔡原, 赵生国. 干扰AdiopR2对藏猪皮下腹股沟脂肪细胞产热的影响[J]. 畜牧兽医学报, 2025, 56(6): 2649-2660.
[6]	武建亮, 苏洋, 毛瑞涵, 周磊, 闫田田, 李智, 刘剑锋. 猪全基因组低密度SNP芯片的设计与效果评价[J]. 畜牧兽医学报, 2025, 56(6): 2733-2740.
[7]	朱爱文, 王健, 朱戈辉, 刘海霞, 平措班旦, 王军, 德庆卓嘎, 闫伟, 韩大勇. 玉米赤霉烯酮致彭波半细毛羊睾丸支持细胞增殖凋亡、氧化应激及NAC保护机制[J]. 畜牧兽医学报, 2025, 56(6): 2752-2764.
[8]	陈志华, 王琪, 张进, 杨连弟, 杨天庆, 王敬, 龙定彪, 黄金秀, 黄文明. 饲粮净能和赖氨酸水平对荣昌母猪妊娠后期繁殖性能、血清激素、泌乳性能及粪便菌群多样性的影响[J]. 畜牧兽医学报, 2025, 56(6): 2801-2815.
[9]	卢会鹏, 曹世诺, 吴植, 陈长春, 陈文玉, 成玉婷, 周晓慧, 孙怀昌, 朱善元. 表达非洲猪瘟病毒基因B602L-B646L的重组病毒免疫原性的初步分析[J]. 畜牧兽医学报, 2025, 56(6): 2816-2825.
[10]	李程程, 赵永祥, 曹秋霞, 宋旭, 李宇鹏, 范宝超, 郭容利, 徐业芬, 李彬. 紧密连接蛋白CLDN4促进猪流行性腹泻病毒感染[J]. 畜牧兽医学报, 2025, 56(6): 2826-2835.
[11]	国德洋, 胡慧, 郑雪莉, 姜艳芬. 猪防御素-1的原核表达及抑菌效应分析[J]. 畜牧兽医学报, 2025, 56(6): 2836-2846.
[12]	王妍, 黄焮榆, 吴桂莹, 吴婉萍, 吕其壮. 2017—2023年我国猪圆环病毒3型的遗传变异分析[J]. 畜牧兽医学报, 2025, 56(6): 2857-2867.
[13]	陈长春, 吴植, 任冠宇, 陈文玉, 曹世诺, 朱睿, 张力, 成玉婷, 朱善元, 卢会鹏. 表达非洲猪瘟pp62与Hsp70蛋白重组腺病毒对小鼠的免疫原性分析[J]. 畜牧兽医学报, 2025, 56(6): 3027-3031.
[14]	陈云龙, 樊港, 樊心怡, 郭永超, 张鑫淼, 王妍, 张仕强. 一株具有多位点核苷酸替换的新型猪圆环病毒2d亚型毒株的分离与鉴定[J]. 畜牧兽医学报, 2025, 56(6): 3032-3040.
[15]	罗嘉, 蒲强, 柴捷, 陈力, 王金勇. 母猪子宫内热应激的生物学效应及遗传机制分析[J]. 畜牧兽医学报, 2025, 56(5): 2004-2014.