𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Liver-specific and high-level expression of human serum amyloid P component gene in transgenic mice

✍ Scribed by Iwanaga, Tomohisa ;Wakasugi, Shoji ;Inomoto, Takeaki ;Uehira, Masahiro ;Ohnishi, Shuji ;Nishiguchi, Seiji ;Araki, Kimi ;Uno, Masashi ;Miyazaki, Jun-Ichi ;Maeda, Shuichiro ;Shimada, Kazunori ;Yamamura, Ken-Ichi


Publisher
John Wiley and Sons
Year
1989
Tongue
English
Weight
644 KB
Volume
10
Category
Article
ISSN
0192-253X

No coin nor oath required. For personal study only.

✦ Synopsis


To analyze the regulation of human serum amyloid P component (SAP) gene expression, we have produced seven transgenic mice. The 3.3 kb human SAP genes containing about 0.8 kb of 5' and 1.5 kb of 3' flanking region were injected into fertilized eggs of C57BL/6 mice. In five of the seven transgenic mice, human SAP was detected in the sera and serum concentrations were higher than that o f human serum in three lines. The human SAP gene was expressed only in the liver. Amounts of human mRNA in the liver and serum concentrations of human SAP were roughly proportional to the copy number of the integrated gene. Human SAP production lowered the serum levels of mouse endogenous SAP. With the intraperitoneal administration o f lipopolysaccharide, the mRNA levels in the liver and serum levels o f mouse SAP increased several-fold in both the control and transgenic mice. O n the other hand, neither the mRNA nor the serum levels of human SAP increased significantly.


πŸ“œ SIMILAR VOLUMES


Glial- and fat-specific expression of th
✍ J.D. Cheng; P. Zhao; A. Espinosa de los Monteros; J. de Vellis πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 884 KB

## Glycerol phosphate dehydrogenase (GPDH) is a metabolic enzyme that catalyzes the conversion of dihy droxyacetone phosphate to glycerol-3-phosphate. It provides phospholipid precursors for lipid biosynthesis and energy metabolism. In the brain, GPDH enzymatic activity, protein, mRNA are exclusiv

Hepatocyte-specific expression of the hu
✍ Alexander J. Smith; J. Marleen de Vree; Roelof Ottenhoff; Ronald P. Elferink; Al πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 524 KB

Mice homozygous for a disruption in the Mdr2 gene (Mdr2 (-/-) mice) lack the Mdr2 P-glycoprotein (P-gp) in the canalicular membrane of the hepatocyte and are unable to excrete phosphatidylcholine into the bile. These mice develop a nonsuppurative cholestatic liver disease, presumably caused by the h