Stetsuk Ye. V., Shepitko V. I., Bilash S. M., Pronina O. M., Boruta N. V., Oliinichenko Ya. O.
CHANGES IN THE NUMBER OF CD 163+ MACROPHAGES IN THE TESTICULAR INTERSTITIUM FOLLOWING CHEMICAL CASTRATION WITH TRIPTORELIN
Show/Download
About the author:
Stetsuk Ye. V., Shepitko V. I., Bilash S. M., Pronina O. M., Boruta N. V., Oliinichenko Ya. O.
Heading:
MORPHOLOGY
Type of article:
Scientific article
Annotation:
The article examines changes in the quantitative parameters of cells of the monocyte-macrophage lineage in the connective tissue of the testis, identified by CD163+ receptors, during chemical castration with triptorelin over a 365-day period. A progressive increase in the number of CD163+ cells (a 3.5-fold increase over one year) indicates the formation of a stable population of M2-phenotype macrophages. This finding reflects a shift in tissue homeostasis toward an anti-inflammatory response and represents an attempt by the organism to compensate for structural damage to the organ parenchyma caused by hormonal imbalance. The most intensive proliferation and migration of CD163+ macrophages occur during the first 90 days and between days 180 and 270 of the experiment. Prolonged accumulation of M2 macrophages at later stages (days 270-365) may have a dual significance: on the one hand, it limits acute inflammation, while on the other, it creates conditions for excessive connective tissue growth (fibrosis), as this macrophage subtype stimulates fibroblast activity. The plateau of this parameter by day 365 indicates the completion of the phase of active cellular mobilization and the achievement of a threshold level of adaptive remodeling of the macrophage reserve under conditions of chronic triptorelin exposure. Changes in CD163+ expression dynamics may serve as a reliable morphological marker of process chronicity and structural remodeling of the testis during the use of gonadotropin-releasing hormone agonists.
Tags:
Bibliography:
- Wang M, Yang Y, Cansever D, Wang Y, Kantores C, Messiaen S, et al. Two populations of self-maintaining monocyte-independent macrophages exist in adult epididymis and testis. 2021;118(1):e2013686117. DOI: 10.1073/pnas.2013686117.
- Mossadegh-Keller N, Sieweke MH. Testicular macrophages: Guardians of fertility. Cell Immunol. 2018;330:120-125. DOI: 10.1016/j.cellimm.2018.03.009.
- Likhachov VK, Vashchenko VL, Taranovska OO. Impact of preventive therapy on regulating mechanisms of decidual macrophage polarization in pregnant women with high risk of preeclamplsia. Wiad Lek. 2021;74(9 cz 1):2123-2127.
- Tkachenkо IM, Dmytrenko MI, Cholovskyi MО, Korovina LD, Mamontova TV. Impregnation of oral mucosa over impacted teeth by subpopulations of macrophages M1 and M2. Wiad Lek. 2021;74(6):1451-1456.
- Yemchenko YaO, Shynkevych VI, Ishcheikin KE, Kaidashev IP. PPAR-Gamma Agonist Pioglitazone Reduced CD68+ but Not CD163+ Macrophage Dermal Infiltration in Obese Psoriatic Patients. PP AR Res. 2020;2020:4548012.
- Zelinka-Khobzey MM, Tarasenko KV, Mamontova TV, Shlykova OA. Characteristics of CD68+ and CD163+ expression in placenta of women with preeclampsia and obesity. Wiad Lek. 2021;74(9 cz 1):2152-2158.
- Balgetir MK, Tektemur NK, Tektemur A, Türk G, Güngör İH, Cihangiroglu AC, et al. Determination of M1/M2 Macrophage Polarization in Ipsilateral and Contralateral Rat Testis Tissue Following Unilateral Torsion/Detorsion. Reprod Sci. 2024;31(7):2092-2102. DOI: 10.1007/s43032-024-01519-6.
- Tsai SJ, Li LH, Chen WJ, Huang EY, Huang CY, Brannigan RE, et al Prediction of microdissection testicular sperm extraction outcomes of azoospermic patients post-chemotherapy using cyclophosphamide equivalent dose. J Assist Reprod Genet. 2023;40(8):2013-2020. DOI: 10.1007/s10815-023-02870-4.
- Garza S, Chen L, Galano M, Cheung G, Sottas C, Li L, et al. Mitochondrial dynamics, Leydig cell function, and age-related testosterone deficiency. FASEB J. 2022;36(12):e22637. DOI: 10.1096/fj.202201026R.
- Li S, Liu L, Luo G, Yuan Y, Hu D, Xiao F. The crosstalk between M1 macrophage polarization and energy metabolism disorder contributes to polystyrene nanoplastics-triggered testicular inflammation. Food Chem Toxicol. 2023;180:114002. DOI: 10.1016/j.fct.2023.114002.
- Botté MC, Lerrant Y, Lozach A, Bérault A, Counis R, Kottler ML. LH down-regulates gonadotropin-releasing hormone (GnRH) receptor, but not GnRH, mRNA levels in the rat testis. J Endocrinol. 1999;162(3):409-415. DOI: 10.1677/joe.0.1620409.
- Stetsuk YeV, Akimov OYe, Shepitko KV, Goltsev AN. Role of nitric oxide in development of fibrotic changes in rats’ testes after 270 day central deprivation of testosterone synthesis. World of medicine and biology. 2020;73(3): 211-215. DOI: 10.26724/2079-8334-2020-3-73-211-215.
- Bahriy MM, Dibrova VA, Popadynets OH, Hryshchuk MI. Metodyky morfolohichnykh doslidzhen. Vinnytsya: Nova knyha; 2016. 328 s. [in Ukrainian].
- Chung JY, Brown S, Chen H, Liu J, Papadopoulos V, Zirkin B. Effects of pharmacologically induced Leydig cell testosterone production on intratesticular testosterone and spermatogenesis. Biol Reprod. 2020;102(2):489-498. DOI: 10.1093/biolre/ioz174.
- Hotta Y, Kataoka T, Kimura K. Testosterone Deficiency and Endothelial Dysfunction: Nitric Oxide, Asymmetric Dimethylarginine, and Endothelial Progenitor Cells. Sex Med Rev. 2019;7(4):661-668. DOI: 10.1016/j.sxmr.2019.02.005.
- Zheng W, Zhang S, Jiang S, Huang Z, Chen X, Guo H, et al. Evaluation of immune status in testis and macrophage polarization associated with testicular damage in patients with nonobstructive azoospermia. Am J Reprod Immunol. 2021;86(5):e13481. DOI: 10.1111/aji.13481.
- Tang Fui MN, Hoermann R, Wittert G, Grossmann M. Testicular volume and clinical correlates of hypothalamic-pituitary-testicular function: A cross-sectional study in obese men. Asian J Androl. 2020;22(4):354-359. DOI: 10.4103/aja.aja_96_19.
Publication of the article:
«Bulletin of problems biology and medicine», 2025 Issue 4, 179, 350-358 pages, index UDC 616.63:477 + 175.67:599.433