Nuclear bodies (NB) are prominent round structures in interchromatin regions of interphase nuclei, regarded as markers of stimulated rRNA synthesis. Their frequency was found to be estrogen-dependent and correlated with estrogen receptor (ER) content in endometrial epithelial cells of prepubertal and cyclic rats. The present study was designed to simultaneously examine the frequency of simple and complex NB and the status of ER in endometrial epithelia of old rats in relation to age and vaginal cytology. The vaginal cycles of old Wistar rats (n degree = 24) at 24, 28, 32, and 36 months of age, which were longitudinally monitored for at least 180 days by daily vaginal smears, were extremely irregular with a predominance of either persistent estrus or persistent diestrus over many days, weeks and even months. In all age groups ER-immunoexpression was very high (+3 = > 75%) in persistent-estrus rats and coincided with particularly frequent NB (2-3 simple NB out of 4-5 total NB per nuclear profile) in the tall epithelial cells with ultrastructural signs of intense protein synthesis. In persistent-diestrus rats isolated simple and complex NB (1 per nuclear profile) and an almost absent ER expression were distinctive of the nuclei in low, ultrastructurally "inactive" endometrial luminal and glandular epithelial cells. Thus, ER immunoexpression and NB frequency are also estrogen-dependent in old rats. Our findings show, for the first time, that ER immunoexpression in endometrial epithelial cells is down-regulated only in old rats in persistent diestrus, whereas in persistent-estrus rats intense ER expression harmonizes with high NB frequency, irrespective of animal age.
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http://dx.doi.org/10.1016/s0039-128x(98)00025-7 | DOI Listing |
JCI Insight
January 2025
Division of Nephrology, Department of Medicine, Vanderbildt University Medical Center, Nashville, United States of America.
Urinary obstruction causes injury to the renal medulla, impairing the ability to concentrate urine, and increasing the risk of progressive kidney disease. However, the regenerative capacity of the renal medulla after reversal of obstruction is poorly understood. To investigate this, we developed a mouse model of reversible urinary obstruction.
View Article and Find Full Text PDFAnn Med
December 2025
School of Basic Medical Sciences, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China.
Angiogenesis is a complex physiological process. In recent years, the immune regulation of angiogenesis has received increasing attention, and innate immune cells, which are centred on macrophages, are thought to play important roles in vascular neogenesis and development. Various innate immune cells can act on the vasculature through a variety of mechanisms, with commonalities as well as differences and synergistic effects, which are crucial for the progression of vascular lesions.
View Article and Find Full Text PDFInvest Ophthalmol Vis Sci
January 2025
Wilmer Eye Institute, Johns Hopkins Medical Institute, Baltimore, Maryland, United States.
Purpose: Although mechanical injury to the cornea (e.g. chronic eye rubbing) is a known risk factor for keratoconus progression, how it contributes to loss of corneal integrity is not known.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
January 2025
Faculty of Life Sciences and Medicine, Harbin Institute of Technology Center for Life Sciences, School of Life Science and Technology, Harbin Institute of Technology, Harbin 150001, China.
Lysophosphatidic acid (LPA) exerts its physiological roles through the endothelialdifferentiation gene (EDG) family LPA receptors (LPAR1-3) or the non-EDG family LPA receptors (LPAR4-6). LPAR6 plays crucial roles in hair loss and cancer progression, yet its structural information is very limited. Here, we report the cryoelectron microscopy structure of LPA-bound human LPAR6 in complex with a mini G or G protein.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
January 2025
Division of Infectious Diseases, Department of Medicine, Brigham and Women's Hospital, Boston, MA 02115.
Epstein-Barr virus (EBV) establishes persistent infection, causes infectious mononucleosis, is a major trigger for multiple sclerosis and contributes to multiple cancers. Yet, knowledge remains incomplete about how the virus remodels host B cells to support lytic replication. We previously identified that EBV lytic replication results in selective depletion of plasma membrane (PM) B cell receptor (BCR) complexes, composed of immunoglobulin and the CD79A and CD79B signaling chains.
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