TY - JOUR
T1 - Differential expression of major gap junction proteins, connexins 26 and 32, in rat mammary glands during pregnancy and lactation
AU - Yamanaka, Ichiro
AU - Kuraoka, Akio
AU - Inai, Tetsuichiro
AU - Ishibashi, Tatsuro
AU - Shibata, Yosaburo
N1 - Funding Information:
Acknowledgements We are very grateful for the generous gift of Cx26 cDNA from Dr. Bruce J. Nicholson (State University of New York, Buffalo, N.Y., USA), of Cx32 cDNA from Dr. David L. Paul (Harvard Medical School, Boston, Mass., USA), and of anti-Cx32 monoclonal antibody from Dr. Akira Takeda (Ehime University, Ehime, Japan). This work was supported in part by grants from Koga Hideya Funds and by Grants-in-Aid for Scientific Research from the Ministry of Education, Science and Culture, Japan (numbers 05454136 and 07407001).
PY - 2001
Y1 - 2001
N2 - We examined the expression pattern of two major gap junction proteins, connexin 26 (Cx26) and connexin 32 (Cx32), in rat mammary glands during pregnancy and lactation. Immunohistochemically the two different Cxs were coexpressed in acinar cells and were independently modulated according to the physiological cell activity. Western blot analysis demonstrated that Cx26 gradually increased from early pregnancy, while Cx32 rapidly and dramatically increased at 16 h after parturition, and that both Cxs reached a maximum early in lactation. Increased expression of both Cxs was confirmed by Northern blot analysis showing that their mRNA transcripts were significantly induced on the day of parturition. We also analyzed double-immunofluorescent staining for Cx26 and Cx32 on a confocal laser scanning microscope, in order to examine colocalization of these Cxs in situ. Cx26 immunoreactivity mostly overlapped with Cx32-positive sites in acinar cells of lactating mammary glands, indicating that both Cxs were colocalized together in the same gap junctional plaques in lactation. These results suggest that upregulation of Cx26 and Cx32 in acinar cells at lactating stages, with colocalization in the same gap junctional plaques, may be important for control of secretion by acinar cells in rat mammary glands.
AB - We examined the expression pattern of two major gap junction proteins, connexin 26 (Cx26) and connexin 32 (Cx32), in rat mammary glands during pregnancy and lactation. Immunohistochemically the two different Cxs were coexpressed in acinar cells and were independently modulated according to the physiological cell activity. Western blot analysis demonstrated that Cx26 gradually increased from early pregnancy, while Cx32 rapidly and dramatically increased at 16 h after parturition, and that both Cxs reached a maximum early in lactation. Increased expression of both Cxs was confirmed by Northern blot analysis showing that their mRNA transcripts were significantly induced on the day of parturition. We also analyzed double-immunofluorescent staining for Cx26 and Cx32 on a confocal laser scanning microscope, in order to examine colocalization of these Cxs in situ. Cx26 immunoreactivity mostly overlapped with Cx32-positive sites in acinar cells of lactating mammary glands, indicating that both Cxs were colocalized together in the same gap junctional plaques in lactation. These results suggest that upregulation of Cx26 and Cx32 in acinar cells at lactating stages, with colocalization in the same gap junctional plaques, may be important for control of secretion by acinar cells in rat mammary glands.
UR - http://www.scopus.com/inward/record.url?scp=0035049208&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0035049208&partnerID=8YFLogxK
U2 - 10.1007/s004180100256
DO - 10.1007/s004180100256
M3 - Article
C2 - 11405055
AN - SCOPUS:0035049208
SN - 0948-6143
VL - 115
SP - 277
EP - 284
JO - Histochemistry and Cell Biology
JF - Histochemistry and Cell Biology
IS - 4
ER -