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M Stambolova

Publications and source records attributed to M Stambolova.

3 recordsLinked to original sources

HMG-2 protein in developing rat brain cells.

1. The distribution of HMG-2 protein was followed in unfractionated rat brain cells at different stages of development. Its amount gradually decreased and reached the lowest level in the terminally differentiated and non-proliferating cells. 2. In isolated oligodendrocyte nuclei the changes in the content of HMG-2 followed the same pattern of distribution which corresponded to their stage of development and proliferative activity, while in the terminally differentiated and non-proliferating cortical neurons a substantial amount of HMG-2 protein was present up to the twenty-eighth postnatal day. 3. In the presence of anti-HMG-2 antibodies the DNA synthetic activity of oligodendrocyte nuclei in vitro was significantly decreased. The treatment with antibodies affected mainly the DNA replicative activity of the nuclei, while their DNA repair activity remained unchanged.

Aging↗

Distribution and metabolic behaviour of "tightly bound" acid-soluble non-histone chromosomal proteins in developing rat brain cells.

"Tightly bound" acid-soluble non-histone chromosomal proteins of rat brain were studied, and limited but detectable tissue specificity of their pattern was demonstrated. This class of proteins showed specific distribution in rat brain cells at different stages of development. The most prominent differences were observed between non-differentiated and terminally differentiated cells. In non-differentiated rat brain cells the acid-soluble non-histone protein fraction contained both metabolically labile and metabolically stable proteins, while in fully developed cells the main portion of acid-soluble proteins showed metabolic stability.

Aging↗

Histone H1o in developing rat brain cells.

Histone H1o was found both in neuronal and oligodendrocyte rat-brain nuclei fractionated by sucrose-gradient isopycnic centrifugation. This histone was absent during the early stages of development when the brain cells were still proliferating, but it appeared in significant amounts in the terminally differentiated cells.

Aging↗