Betaine transporter cdna cloning and effect of osmolytes on its
mrna induction.
Ferraris, Joan D., Maurice B. Burg, Chester K. Williams, Eugenia M.
Peters, and Arlyn Garc[acute]ia-P[acute]erez.
Laboratory of Kidney and Electrolyte Metabolism, National Heart,
Lung, and Blood Institute, National Institutes of Health, Bethesda,
MD 20892-1598
APStracts 2:0327C, 1995.
Cells generally adapt to long term hyperosmolality by accumulating
compatible organic osmolytes thereby helping to normalize both volume
and intracellular inorganic io concentration. When organic osmolytes
are accumulated, as in renal inner medullary cells, it is the sum of
their concentrations that is theoretically important. In effect, when
one organic osmolyte rises, the others generally fall to maintain
their sum approximately constant. The present study addresses the
mechanism controlling betaine accumulation. Hypertonicity induces
accumulation of betaine, sorbitol, inositol, and other organic
osmolytes in PAP-HT25 cells, a line derived from rabbit renal
papilla. Hypertonicity increases the betaine transporter expression
in these cells. To obtain a specific probe for betaine transporter
mRNA, we cloned from PAP-HT25 cells a cDNA that encodes the full
protein. We then examined the effect of betaine, sorbitol, and
inositol on betaine transporter mRNA abundance. Increased
accumulation of any of these three organic osmolytes reduces betaine
transporter mRNA. We previously observed similar results for aldose
reductase, the enzyme responsible for osmotically regulated sorbitol
accumulation. We conclude that the accumulation of organic osmolytes
regulates betaine transporter gene expression. Since the aldose
reductase gene is controlled in a similar fashion, we surmise that
the two genes share a common signal for induction.
Received 25 May 1995; accepted in final form 21 August 1995.
APS Manuscript Number C304-5.
Article publication pending Am. J. Physiol. (Cell Physiology).
ISSN 1080-4757 Copyright 1995 The American Physiological Society.
Published in APStracts on 23 September 1995.