Late human cytomegalovirus (HCMV) proteins inhibit differentiation of human neural precursor cells into astrocytes

• Published in: Journal of neuroscience research 2007-02, Vol.85 (3), p.583-593
• Main Authors: Odeberg, Jenny, Wolmer, Nina, Falci, Scott, Westgren, Magnus, Sundtröm, Erik, Seiger, Åke, Söderberg-Nauclér, Cecilia
• Format: Article
• Language: English
• Subjects: Abortion, Induced; apoptosis; Apoptosis - drug effects; astrocytes; Astrocytes - cytology; Astrocytes - drug effects; Astrocytes - physiology; Cell Differentiation - drug effects; cytomegalovirus; Cytomegalovirus - physiology; Cytomegalovirus Infections - embryology; Cytomegalovirus Infections - transmission; differentiation; Female; Flow Cytometry; Humans; Medicin och hälsovetenskap; Pregnancy; Prosencephalon - cytology; Prosencephalon - drug effects; Prosencephalon - embryology; Prosencephalon - virology; stem cells; Viral Proteins - pharmacology
• ISSN: 0360-4012; 1097-4547
• DOI: 10.1002/jnr.21144

Human cytomegalovirus (HCMV) is the most common cause of congenital infections in developed countries, with an incidence varying between 0.5–2.2%. Such infection may be the consequence of either a primary infection or reactivation of a latent infection in the mother and the outcome may vary from asymptomatic to severe brain disorders. Moreover, infants that are asymptomatic at the time of birth may still develop neurologic sequelae at a later age. Our hypothesis is that infection of stem cells of the central nervous system by HCMV alters the proliferation, differentiation or migration of these cells, and thereby gives rise to the brain abnormalities observed. We show that infection of human neural precursor cells (NPCs) with the laboratory strain Towne or the clinical isolate TB40 of HCMV suppresses the differentiation of these cells into astrocytes even at an multiplicity of infection (MOI) as low as 0.1 (by 33% and 67%, respectively). This inhibition required active viral replication and the expression of late HCMV proteins. Infection as late as 24 hr after the onset of differentiation, but not after 72 hr, also prevented the maturation of infected cultures. Furthermore, in cultures infected with TB40 (at an MOI of 1), approximately 54% of the cells were apoptotic and cell proliferation was significantly attenuated. Clearly, HCMV can reduce the capacity of NPCs to differentiate into astrocytes and this effect may provide part of the explanation for the abnormalities in brain development associated with congenital HCMV infection. © 2006 Wiley‐Liss, Inc.