A student laboratory exercise illustrating active transport across the small intestine

1965 ◽  
Vol 20 (5) ◽  
pp. 1102-1105 ◽  
Author(s):  
T. Hastings Wilson ◽  
Angela DeCarlo

A 7-year experience with student laboratory exercises dealing with intestinal transport in vitro is described. A single experiment which has evolved from trial and error in the student laboratory is given in detail. Everted sacs of small intestine from the golden hamster are incubated in flasks containing bicarbonate-saline with 10 mm glucose and 2 mm d- or l-tyrosine. Glucose and l-tyrosine are transported across the intestinal wall against concentration gradients; d-tyrosine is not, illustrating the stereospecificity of the amino acid transport system. A second experiment which illustrates the stimulation of vitamin B12 absorption by gastric intrinsic factor is briefly recorded. The student interest aroused and the high degree of satisfactory results make such experiments useful additions to the repertoire of student laboratory exercises in physiology. intestinal transport; amino acid transport; B12 transport Submitted on November 12, 1964

1993 ◽  
Vol 28 (3) ◽  
pp. 261-266 ◽  
Author(s):  
K. Hayashi ◽  
H. Amioka ◽  
J. I. Kurokawa ◽  
Y. Kuga ◽  
S. I. Nomura ◽  
...  

2021 ◽  
Vol 85 (3) ◽  
pp. 587-599
Author(s):  
Akane Sato ◽  
Takumi Kimura ◽  
Kana Hondo ◽  
Miyuki Kawano-Kawada ◽  
Takayuki Sekito

ABSTRACT In Saccharomyces cerevisiae, Avt4 exports neutral and basic amino acids from vacuoles. Previous studies have suggested that the GATA transcription factors, Gln3 and Gat1, which are key regulators that adapt cells in response to changes in amino acid status, are involved in the AVT4 transcription. Here, we show that mutations in the putative GATA-binding sites of the AVT4 promoter reduced AVT4 expression. Consistently, a chromatin immunoprecipitation (ChIP) assay revealed that Gat1-Myc13 binds to the AVT4 promoter. Previous microarray results were confirmed that gln3∆gat1∆ cells showed a decrease in expression of AVT1 and AVT7, which also encode vacuolar amino acid transporters. Additionally, ChIP analysis revealed that the AVT6 encoding vacuolar acidic amino acid exporter represents a new direct target of the GATA transcription factor. The broad effect of the GATA transcription factors on the expression of AVT transporters suggests that vacuolar amino acid transport is integrated into cellular amino acid homeostasis.


2001 ◽  
Vol 283 (1) ◽  
pp. 174-178 ◽  
Author(s):  
Roberta R. Alfieri ◽  
Pier-Giorgio Petronini ◽  
Mara A. Bonelli ◽  
Alessandro E. Caccamo ◽  
Andrea Cavazzoni ◽  
...  

2002 ◽  
Vol 282 (1) ◽  
pp. C196-C204 ◽  
Author(s):  
Yoko Okamoto ◽  
Masahiro Sakata ◽  
Kazuhiro Ogura ◽  
Toshiya Yamamoto ◽  
Masaaki Yamaguchi ◽  
...  

The neutral amino acid transport system L is a sodium-independent transport system in human placenta and choriocarcinoma cells. Recently, it was found that the heterodimer composed of hLAT1 (a light-chain protein) and 4F2 heavy chain (4F2hc), a type II transmembrane glycoprotein, is responsible for system L amino acid transport. We found that the mRNAs of 4F2hc and hLAT1 were expressed in the human placenta and a human choriocarcinoma cell line. The levels of the 4F2hc and hLAT1 proteins in the human placenta increased at full term compared with those at midtrimester. Immunohistochemical data showed that these proteins were localized mainly in the placental apical membrane. Data from leucine uptake experiments, Northern blot analysis, and immunoblot analysis showed that this transport system was partially regulated by protein kinase C and calcium ionophore in the human choriocarcinoma cell line. Our results suggest that the heterodimer of 4F2hc and hLAT1 may play an important role in placental amino acid transport system L.


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