{"title":"Immunohistochemical and ultrastructural analysis of macrophages during cyclic corpus luteum formation and regression in Indian Buffalo","authors":"Kritima Kapoor, Opinder Singh, Devendra Pathak","doi":"10.1007/s10735-025-10573-6","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>The present research was conducted on corpora lutea (CL) samples of healthy buffaloes (<i>n</i> = 24) with the aim to localize presence of immune cell macrophage, immunohistochemically and ultrastructurally. The collected CL were categorized into four different stages i.e., early (stage I, 1 to 5 days, <i>n</i> = 6), mid (stage II, 6 to 11 days, <i>n</i> = 6), late luteal phase (stage III, 12 to 16 days, <i>n</i> = 6) and regressing phase (stage IV, 17 to 20 days, <i>n</i> = 6), based on their gross morphology. The macrophages were observed occasionally throughout the luteal parenchyma of early and mid-luteal CL. However, their number was lowest during early and mid-luteal phases being 7.7 ± 0.98 (Mean ± S.E) and 6.37 ± 0.79 per unit area, respectively. The number was considerably higher in regressing phases i.e., late luteal phase (60.45 ± 4.39 per unit area) and corpus albicans (108.25 ± 6.35 per unit area). Ultrastructurally as well, their presence was observed to be higher in the regressing phases as cells with filopdia for the process of phagocytosis. These findings concluded that the presence of macrophages, although lower in early and mid-luteal phases of CL formation, indicated their probable role in promoting angiogenesis and thus proliferation of buffalo CL during its formation. However, their considerable higher presence during late and regressing phases of CL led to increased phagocytosis of degraded luteal cells that thereby promoted its structural luteolysis.</p>\n </div>","PeriodicalId":650,"journal":{"name":"Journal of Molecular Histology","volume":"56 5","pages":""},"PeriodicalIF":2.2000,"publicationDate":"2025-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Molecular Histology","FirstCategoryId":"99","ListUrlMain":"https://link.springer.com/article/10.1007/s10735-025-10573-6","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The present research was conducted on corpora lutea (CL) samples of healthy buffaloes (n = 24) with the aim to localize presence of immune cell macrophage, immunohistochemically and ultrastructurally. The collected CL were categorized into four different stages i.e., early (stage I, 1 to 5 days, n = 6), mid (stage II, 6 to 11 days, n = 6), late luteal phase (stage III, 12 to 16 days, n = 6) and regressing phase (stage IV, 17 to 20 days, n = 6), based on their gross morphology. The macrophages were observed occasionally throughout the luteal parenchyma of early and mid-luteal CL. However, their number was lowest during early and mid-luteal phases being 7.7 ± 0.98 (Mean ± S.E) and 6.37 ± 0.79 per unit area, respectively. The number was considerably higher in regressing phases i.e., late luteal phase (60.45 ± 4.39 per unit area) and corpus albicans (108.25 ± 6.35 per unit area). Ultrastructurally as well, their presence was observed to be higher in the regressing phases as cells with filopdia for the process of phagocytosis. These findings concluded that the presence of macrophages, although lower in early and mid-luteal phases of CL formation, indicated their probable role in promoting angiogenesis and thus proliferation of buffalo CL during its formation. However, their considerable higher presence during late and regressing phases of CL led to increased phagocytosis of degraded luteal cells that thereby promoted its structural luteolysis.
期刊介绍:
The Journal of Molecular Histology publishes results of original research on the localization and expression of molecules in animal cells, tissues and organs. Coverage includes studies describing novel cellular or ultrastructural distributions of molecules which provide insight into biochemical or physiological function, development, histologic structure and disease processes.
Major research themes of particular interest include:
- Cell-Cell and Cell-Matrix Interactions;
- Connective Tissues;
- Development and Disease;
- Neuroscience.
Please note that the Journal of Molecular Histology does not consider manuscripts dealing with the application of immunological or other probes on non-standard laboratory animal models unless the results are clearly of significant and general biological importance.
The Journal of Molecular Histology publishes full-length original research papers, review articles, short communications and letters to the editors. All manuscripts are typically reviewed by two independent referees. The Journal of Molecular Histology is a continuation of The Histochemical Journal.