磷酸盐
细胞培养
生物化学
圆周率
佛波
化学
生物
蛋白激酶C
酶
遗传学
标识
DOI:10.1002/jcp.1041350117
摘要
Abstract The LLC‐PK 1 cell line transports phosphate (Pi), glucose, and amino acids using carriers similar to those in proximal tubular cells. Others have reported that when monolayers reach confluence, hexose transport increases and activity of the A‐amino acid transporter falls. The present study evaluates Pi uptake by two continuous cell lines derived from renal proximal tubule, and demonstrates that phosphate uptake falls sharply upon reaching confluence in LLC‐PK 1 cells but not in cultured opossum kidney (OK) cells. The fall in Pi uptake in LLC‐PK 1 cells at confluence represents a halving in V max for Na‐dependent phosphate uptake (2.33 vs. 5.00 nmol/mg protein/5 min) without a change in Km (82 vs. 94 μM). Suppression of phosphate transport in confluent monolayers of LLC‐PK 1 cells is completely reversed by bringing the cells into suspension. As has been shown for the phorbol ester 12‐O‐tetradecanoyl‐phorbol‐13‐acetate (TPA), exposure of monolayers to serum stimulates phosphate uptake, but unlike phorbol ester, serum does so without stimulating alanine uptake. OK cells differ from LLC‐PK 1 in that no change occurs in Pi uptake at confluence, although they resemble LLC‐PK 1 cells in that sugar uptake rises and alanine uptake falls at confluence. The different temporal patterns for Pi uptake in the two cell lines indicates that developmental change in the uptake of Pi is not linked to that of glucose or alanine.
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