Developmental Changes in Gap Junction Expression in Rat Adrenal Medullary Chromaffin Cells
Cell-to-cell communications are desirable for efficient functioning in endocrine cells. Gap junctions and paracrine factors are major mechanisms by which neighboring endocrine cells communicate with each other. The current experiment was undertaken to morphologically examine gap junction expression...
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Published in | Acta histochemica et cytochemica Vol. 57; no. 6; pp. 189 - 197 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Japan
Japan Science and Technology Agency
20.12.2024
JAPAN SOCIETY OF HISTOCHEMISTRY AND CYTOCHEMISTRY |
Subjects | |
Online Access | Get full text |
ISSN | 0044-5991 1347-5800 |
DOI | 10.1267/ahc.24-00033 |
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Summary: | Cell-to-cell communications are desirable for efficient functioning in endocrine cells. Gap junctions and paracrine factors are major mechanisms by which neighboring endocrine cells communicate with each other. The current experiment was undertaken to morphologically examine gap junction expression and developmental changes in rat adrenal medullary chromaffin (AMC) cells. The expression of connexin 43 (Cx43) was conspicuous in the rat adrenal cortex, but not detected immunohistochemically in neonatal or adult AMC cells. Consistent with the morphological findings, the phosphorylated and non-phosphorylated forms of Cx43 were predominantly and faintly detected by immunoblotting in the adrenal cortical and medullary homogenates, respectively. In contrast to Cx43, Cx36-like immunoreactive (IR) material was detected in neonatal AMC cells, a fraction of which were in the process of migration to the center of the adrenal gland, but this was not seen in adult AMC cells. The current results raise the possibility that the mechanism for cell-to-cell communication changes in a developmental manner in rat AMC cells. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 0044-5991 1347-5800 |
DOI: | 10.1267/ahc.24-00033 |