𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Analysis of activin A gene expression in human bone marrow stromal cells

✍ Scribed by Karen E. Dolter; Julie C. Palyash; Li-En Shao; John Yu


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
253 KB
Volume
70
Category
Article
ISSN
0730-2312

No coin nor oath required. For personal study only.

✦ Synopsis


Activin A, a member of the TGF-␀ superfamily, plays roles in differentiation and development, including hematopoiesis. Our previous studies indicated that the expression of activin A by human bone marrow cells and monocytes is highly regulated by inflammatory cytokines and glucocorticoids. The present study was undertaken to investigate the regulation of activin A gene expression in the human bone marrow stromal cell lines L87/4 and HS-5, as well as in primary stromal cells. Northern blots demonstrated that, like primary stromal cells, the cell lines expressed four activin A RNA transcripts (6.4, 4.0, 2.8, and 1.6 kb), although distribution of the RNA among the four sizes varied. The locations of the 5' ends of the RNAs were investigated by Northern blots and RNase protection assays. The results identified a transcription start site at 212 nucleotides upstream of the translation start codon. In addition, luciferase expression assays of a series of deletion constructs were used to identify regulatory sequences upstream of the activin A gene. A 58 bp upstream sequence exhibits promoter activity. However, severalfold higher expression requires a positive element consisting of an additional 71 bp of the upstream region. Promoter activity was also identified between 2.5 and 3.6 kb upstream of the start codon. These findings suggest that expression of activin A at the transcriptional level follows complex patterns of regulation.


πŸ“œ SIMILAR VOLUMES


Receptor tyrosine kinase expression in h
✍ Kazuhito Satomura; Anna R. Derubeis; Neal S. Fedarko; Kyomi Ibaraki-O'Connor; Se πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 468 KB πŸ‘ 1 views

Bone marrow stromal cells (BMSCs) are a heterogeneous population of cells derived from colony-forming units-fibroblastic (CFU-Fs). These cells reside in the bone marrow cavity and are capable of differentiating into several cell phenotypes including osteoblasts, chondroblasts, hematopoiesis-supporti

Biocompatibility analysis of different b
✍ Wilke, A. ;Orth, J. ;Lomb, M. ;Fuhrmann, R. ;Kienapfel, H. ;Griss, P. ;Franke, R πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 195 KB πŸ‘ 1 views

A cell culture system for biocompatibility testing of hip implant materials is described. Human bone marrow cells have been chosen because these cells are in direct contact with the biomaterial after implantation in situ. The sensitivity of this method is evaluated for materials which are already be

Differential display of human marrow str
✍ Suzanne C. DieudonnΓ©; Janet M. Kerr; Tianshun Xu; Beatrice Sommer; Anna R. DeRub πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 383 KB πŸ‘ 2 views

Human bone marrow stromal cells (hBMSC) are pluripotent cells that have the ability to differentiate into bone, cartilage, hematopoietic-supportive stroma, and adipocytes in a process modulated by dexamethasone (DEX). To characterize changes in hBMSC in response to DEX, we carried out differential d

Serial analysis of gene expression in a
✍ Haruhisa Inoue; Makoto Sawada; Akihide Ryo; Hiroshi Tanahashi; Toru Wakatsuki; A πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 121 KB πŸ‘ 2 views

We used the serial analysis of gene expression (SAGE) method to systematically analyze transcripts present in a microglial cell line. Over 10,000 SAGE tags were sequenced, and shown to represent 6,013 unique transcripts. Among the diverse transcripts that had not been previously detected in microgli