TY - JOUR
T1 - Luminal localization of blood-brain barrier sodium, potassium adenosine triphosphatase is dependent on fixation
AU - Manoonkitiwongsa, Panya S.
AU - Schultz, Robert L.
AU - Wareesangtip, Wanpen
AU - Whitter, Ernest F.
AU - Nava, Pedro B.
AU - McMillan, Paul J.
PY - 2000/6
Y1 - 2000/6
N2 - Cytochemical data in the literature reporting localization of sodium, potassium adenosine triphosphatase (Na+, K+-ATPase) in the blood-brain barrier (BBB) have been contradictory. Whereas some studies showed the enzyme to be located exclusively on the abluminal endothelial plasma membrane, others demonstrated it on both the luminal and abluminal membranes. The influence of fixation on localization of the enzyme was not considered a critical factor, but our preliminary studies showed data to the contrary. We therefore quantitatively investigated the effect of commonly used fixatives on the localization pattern of the enzyme in adult rat cerebral microvessels. Fixation with 1%, 2%, and 4% formaldehyde allowed deposition of reaction product on both the luminal and abluminal plasma membranes. The luminal reaction was reduced with increasing concentration of formaldehyde. Glutaraldehyde at 0.1%, 0.25%, 0.5%, in combination with 2% formaldehyde, drastically inhibited the luminal reaction. The abluminal reaction was not significantly altered in all groups. These results show that luminal localization of BBB Na+, K+-ATPase is strongly dependent on fixation. The lack of luminal localization, as reported in the literature, may have been the result of fixation. The currently accepted abluminal polarity of the enzyme should be viewed with caution.
AB - Cytochemical data in the literature reporting localization of sodium, potassium adenosine triphosphatase (Na+, K+-ATPase) in the blood-brain barrier (BBB) have been contradictory. Whereas some studies showed the enzyme to be located exclusively on the abluminal endothelial plasma membrane, others demonstrated it on both the luminal and abluminal membranes. The influence of fixation on localization of the enzyme was not considered a critical factor, but our preliminary studies showed data to the contrary. We therefore quantitatively investigated the effect of commonly used fixatives on the localization pattern of the enzyme in adult rat cerebral microvessels. Fixation with 1%, 2%, and 4% formaldehyde allowed deposition of reaction product on both the luminal and abluminal plasma membranes. The luminal reaction was reduced with increasing concentration of formaldehyde. Glutaraldehyde at 0.1%, 0.25%, 0.5%, in combination with 2% formaldehyde, drastically inhibited the luminal reaction. The abluminal reaction was not significantly altered in all groups. These results show that luminal localization of BBB Na+, K+-ATPase is strongly dependent on fixation. The lack of luminal localization, as reported in the literature, may have been the result of fixation. The currently accepted abluminal polarity of the enzyme should be viewed with caution.
KW - Blood-brain barrier
KW - Enzyme cytochemistry
KW - Fixation
KW - Na, K-ATPase
UR - https://www.scopus.com/pages/publications/0034044426
UR - https://www.scopus.com/pages/publications/0034044426#tab=citedBy
U2 - 10.1177/002215540004800614
DO - 10.1177/002215540004800614
M3 - Article
C2 - 10820159
SN - 0022-1554
VL - 48
SP - 859
EP - 865
JO - Journal of Histochemistry and Cytochemistry
JF - Journal of Histochemistry and Cytochemistry
IS - 6
ER -