The localization of connexin43 (Cx 43) in rat kidney was investigated by the indirect immunofluorescence technique with polyclonal antisera raised against Cx 43. Cx 43 is a gap junction protein expressed in a variety of tissues. The typically punctuated gap junction immunofluorescence (GJI) was observed in the renal arterial and arteriolar system. In the renal artery the GJI was concentrated in the media. In the juxtamedullary nephrons, the GJI is particularly abundant in the vascular bundles. There is abundant GJI in the extraglomerular mesangium while in the afferent arteriole GJI appears decreased. Abundant GJI was observed in the inner medullary collecting ducts and pelvic epithelium. The localization of Cx 43 immunofluorescence observed in this study is only in partial agreement with the results of ultrastructural investigations on the distribution of gap junctions in the kidney. An extensive tight junctional system has been demonstrated in the collecting duct system. However, gap junctions have been reported to be absent. Further studies to resolve this discrepancy are required.
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http://dx.doi.org/10.1038/ki.1994.314 | DOI Listing |
ACS Biomater Sci Eng
January 2025
Electrical and Computer Engineering, University of Virginia, Charlottesville, Virginia 22904, United States.
Cardiovascular diseases remain the leading cause of mortality, necessitating advancements in cardiac tissue engineering platforms for improved disease modeling, drug screening, and regenerative therapies. The chief challenge to recapitulating the beating behavior of cardiomyocytes is creation of the circular stress profile experienced by hollow organs in the natural heart due to filling pressure and integrated strategies for intercellular communication to promote cell-to-cell connections. We present a platform featuring addressable arrays of nanogrooved polydimethylsiloxane (PDMS) diaphragms for cell alignment and circular mechanical stimulation, with embedded silver nanowires (AgNWs) for electrical cues, so that cardiomyocyte functionality can be assessed under these synergistic influences.
View Article and Find Full Text PDFPrenat Diagn
January 2025
Centre for Bioengineering, School of Engineering and Materials Science, Queen Mary University of London, London, UK.
Objective: We examined the role of myofibroblasts in regulating Cx43 and collagen structure in iatrogenic preterm amniotic membrane (AM) defects subjected to mechanical stimulation.
Method: Preterm AM specimens were collected from women undergoing planned preterm caesarean section after in utero intervention for correction of spina bifida by open fetal surgery (n = 4 patients; preterm delivery at 34 + 0 weeks to 35 + 0 weeks). Control specimens taken 5 cm away from the open fetal surgery defect site were compared with wound edge AM.
Anal Cell Pathol (Amst)
December 2024
Department of Orthopedics, Jincheng General Hospital, China Kangping Street, Beishidian Town, Jincheng 048006, China.
bioRxiv
October 2024
The Department of Cell Biology, Duke University Medical Center, Durham, NC, USA.
Medicina (Kaunas)
October 2024
Department of R&D, Stem Biotechnology Inc., 12F-2, Building F, No. 3, Park Street, Nangang District, Taipei 115, Taiwan.
: The Connexin43 () gene is a suspected tumor suppressor gene, as re-expressed wild-type genes reduce the malignancy potential of tumor cells. However, the role of gene expression in human lung tumorigenesis remains unclear. Tumor tissues from 165 primary lung cancer patients were collected to study Cx43 protein expression and gene mutations using immunohistochemistry and direct DNA sequencing.
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