## Abstract The objective of the study was to evaluate the distributions of (1) cells expressing the contractile actin isoform, α‐smooth muscle actin (α‐SMA) and (2) a lubricating and antiadhesion glycoprotein, lubricin, in the tissue around loose joint replacement prostheses in human subjects. Per
α Isoform of smooth muscle actin is expressed in astrocytes in vitro and in vivo
✍ Scribed by E. Lecain; F. Alliot; M. C. Laine; B. Calas; Dr. B. Pessac
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 562 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0360-4012
No coin nor oath required. For personal study only.
✦ Synopsis
We have previously reported that astroglial cell lines derived from spontaneously immortalized mouse cerebellar cultures as well as primary astrocyte cultures express the mRNA of the a isoform of smooth muscle actin. In this report, we have used an antiserum specific for the a smooth muscle actin protein to investigate the presence and the pattern of expression of a smooth muscle actin protein at the cellular level with immunocytochemical methods. The results show that an anti-smooth muscle vessels a actin antiserum labels a typical actin network in the D19 astroglial cell clone and in flat astrocytes of primary cultures derived from various CNS regions of embryonic and postnatal mice. Furthermore, this antiserum labels distinct populations of astrocytes in the adult mouse brain, in particular in the corpus callosum and the fornix. However, in the corpus callosum, astrocytic processes are strongly labeled by anti-SMV a actin antibodies only in parasagittal planes. Thus, a smooth muscle actin represents a new marker for subsets of astrocytes.
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