TY - JOUR
T1 - Expression of apical Na+–l-glutamine co-transport activity, B0-system neutral amino acid co-transporter (B0AT1) and angiotensin-converting enzyme 2 along the jejunal crypt–villus axis in young pigs fed a liquid formula
AU - Yang, Chengbo
AU - Yang, Xiaojian
AU - Lackeyram, Dale
AU - Rideout, Todd C.
AU - Wang, Zirong
AU - Stoll, Barbara
AU - Yin, Yulong
AU - Burrin, Douglas G.
AU - Fan, Ming Z.
N1 - Publisher Copyright:
© 2016, Springer-Verlag Wien.
PY - 2016/6/1
Y1 - 2016/6/1
N2 - Gut apical amino acid (AA) transport activity is high at birth and during suckling, thus being essential to maintain luminal nutrient-dependent mucosal growth through providing AA as essential metabolic fuel, substrates and nutrient stimuli for cellular growth. Because system-B0 Na+–neutral AA co-transporter (B0AT1, encoded by the SLC6A19 gene) plays a dominant role for apical uptake of large neutral AA including l-Gln, we hypothesized that high apical Na+–Gln co-transport activity, and B0AT1 (SLC6A19) in co-expression with angiotensin-converting enzyme 2 (ACE2) were expressed along the entire small intestinal crypt–villus axis in young animals via unique control mechanisms. Kinetics of Na+–Gln co-transport activity in the apical membrane vesicles, prepared from epithelial cells sequentially isolated along the jejunal crypt–villus axis from liquid formula-fed young pigs, were measured with the membrane potential being clamped to zero using thiocyanate. Apical maximal Na+–Gln co-transport activity was much higher (p < 0.05) in the upper villus cells than in the middle villus (by 29 %) and the crypt (by 30 %) cells, whereas Na+–Gln co-transport affinity was lower (p < 0.05) in the upper villus cells than in the middle villus and the crypt cells. The B0AT1 (SLC6A19) mRNA abundance was lower (p < 0.05) in the crypt (by 40–47 %) than in the villus cells. There were no significant differences in B0AT1 and ACE2 protein abundances on the apical membrane among the upper villus, the middle villus and the crypt cells. Our study suggests that piglet fast growth is associated with very high intestinal apical Na+–neutral AA uptake activities via abundantly co-expressing B0AT1 and ACE2 proteins in the apical membrane and by transcribing the B0AT1 (SLC6A19) gene in the epithelia along the entire crypt–villus axis.
AB - Gut apical amino acid (AA) transport activity is high at birth and during suckling, thus being essential to maintain luminal nutrient-dependent mucosal growth through providing AA as essential metabolic fuel, substrates and nutrient stimuli for cellular growth. Because system-B0 Na+–neutral AA co-transporter (B0AT1, encoded by the SLC6A19 gene) plays a dominant role for apical uptake of large neutral AA including l-Gln, we hypothesized that high apical Na+–Gln co-transport activity, and B0AT1 (SLC6A19) in co-expression with angiotensin-converting enzyme 2 (ACE2) were expressed along the entire small intestinal crypt–villus axis in young animals via unique control mechanisms. Kinetics of Na+–Gln co-transport activity in the apical membrane vesicles, prepared from epithelial cells sequentially isolated along the jejunal crypt–villus axis from liquid formula-fed young pigs, were measured with the membrane potential being clamped to zero using thiocyanate. Apical maximal Na+–Gln co-transport activity was much higher (p < 0.05) in the upper villus cells than in the middle villus (by 29 %) and the crypt (by 30 %) cells, whereas Na+–Gln co-transport affinity was lower (p < 0.05) in the upper villus cells than in the middle villus and the crypt cells. The B0AT1 (SLC6A19) mRNA abundance was lower (p < 0.05) in the crypt (by 40–47 %) than in the villus cells. There were no significant differences in B0AT1 and ACE2 protein abundances on the apical membrane among the upper villus, the middle villus and the crypt cells. Our study suggests that piglet fast growth is associated with very high intestinal apical Na+–neutral AA uptake activities via abundantly co-expressing B0AT1 and ACE2 proteins in the apical membrane and by transcribing the B0AT1 (SLC6A19) gene in the epithelia along the entire crypt–villus axis.
KW - Angiotensin-converting enzyme 2
KW - Gut crypt–villus axis
KW - SLC6A19
KW - Small intestinal apical l-glutamine uptake
KW - System-B Na–neutral amino acid co-transporter
UR - http://www.scopus.com/inward/record.url?scp=84961203039&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84961203039&partnerID=8YFLogxK
U2 - 10.1007/s00726-016-2210-7
DO - 10.1007/s00726-016-2210-7
M3 - Article
C2 - 26984322
AN - SCOPUS:84961203039
SN - 0939-4451
VL - 48
SP - 1491
EP - 1508
JO - Amino Acids
JF - Amino Acids
IS - 6
ER -