Lazarini F, Deslys J P, Dormont D
Laboratoire de Neuropathologie Expérimentale, CRSSA, DSV/DPTE, Commissariat à l'Energie Atomique, Fontenay aux Roses, France.
J Gen Virol. 1992 Jul;73 ( Pt 7):1645-8. doi: 10.1099/0022-1317-73-7-1645.
To begin to understand the molecular basis of cases of Creutzfeldt-Jakob disease recently described in young children, the expression of prion protein and glial fibrillary acidic protein (GFAP) mRNAs was investigated during the development of the brain of scrapie-infected newborn mice. Changes in the time course of expression were identified by Northern blot quantification between days 1 and 172. Although scrapie-infected and control animals showed no detectable changes in brain development (first 56 days of life), GFAP mRNAs were found to increase significantly as early as day 84. A 10-fold increase in the level of GFAP mRNA was observed in brain between day 112 and death (day 172).