G. Estrada et al., QUANTITATIVE-ANALYSIS OF LACTASE-PHLORHIZIN HYDROLASE EXPRESSION IN THE ABSORPTIVE ENTEROCYTES OF NEWBORN RAT SMALL-INTESTINE, Journal of cellular physiology, 167(2), 1996, pp. 341-348
At birth, the mammalian small intestine displays regional differences
in morphology as well as complex proximal-to-distal (horizontal) patte
rns of protein distribution. Lactase-phlorizin hydrolase (LPH), an ent
erocyte-specific disaccharidase crucial for the digestion of lactose i
n milk, reveals a characteristic horizontal pattern of expression at b
irth. However, it is not certain whether this topographic pattern is d
ue to variations in epithelial structure along the length of the small
intestine or to regional differences in the transcription of the LPH
gene. In order to understand the mechanisms that regulate the regional
ization of LPH at birth, we characterized the epithelial structure alo
ng the horizontal axis using stereologic techniques and correlated the
se data with the patterns of lactase activity and LPH mRNA abundance i
n the small intestine of unsuckled, newborn rats. Epithelial volume an
d microvillar surface area per unit of intestinal length decreased thr
ee-to fourfold from duodenum to distal ileum. In contrast, lactase act
ivity and LPH mRNA abundance were highest in proximal jejunum and lowe
st in the most proximal and distal ends of the small intestine. Mean l
actase activity per cell in proximal duodenum, proximal jejunum, and d
istal ileum was estimated at 12.0, 26.7, and 5.6 nU/absorptive enteroc
yte, respectively, and paralleled the concentration of LPH mRNA in the
same segments: 20, 45, and 15 molecules of LPH mRNA/absorptive entero
cyte. Our data indicate that horizontal gradients of lactase activity
in the newborn rat intestine do not depend on epithelial organization
or on enteral factors, since the horizontal gradient is established be
fore suckling. Each absorptive enterocyte along the small intestine ex
presses lactase activity in a position-dependent manner which is contr
olled at the level of mRNA abundance. (C) 1996 Wiley-Liss, Inc.