A distal to proximal gradient of human choroid plexus development, with antagonistic expression of Glut1 and AQP1 in mature cells versus calbindin and PCNA in proliferative cells

• Published in: Frontiers in neuroanatomy Vol. 10
• Main Authors: Leandro Castañeyra-Ruiz, Ibrahim Gonzalez-Marrero, Luis G Hernandez-Abad, Emilia M Carmona-Calero, Gundela Meyer, Agustin Castañeyra-Perdomo
• Format: Journal Article
• Language: English
• Published: Frontiers Media S.A 01.09.2016
• Subjects: aquaporin-1; calbindin; Choroid plexus development; GLUT1; PCNA
• ISSN: 1662-5129
• DOI: 10.3389/fnana.2016.00087

The choroid plexuses (ChP) are highly vascularized tissues suspended from each of the cerebral ventricles. Their main function is to secret CSF that fills the ventricles and the subarachnoid spaces, forming a crucial system for the development and maintenance of the CNS. However, despite the essential role of the ChP–CSF system to regulate the CNS in a global manner, it still remains one of the most understudied areas in neurobiology. Here we define by immunohistochemistry the expression of different proteins involved in the maturation and functionality of the ChP from the late embryological period to maturity. We found an opposite gradient of expression between AQP1 and Glut1 that define functional maturation in the ChP periphery, and PCNA and calbindin, present in the ChP roof zone with proliferative activity. We conclude that the maturation of the ChP matures from distal to proximal, starting in the areas nearest to the cortex, expressing in the distal, mature areas AQP1 and Glut1 (related to ChP functionality to support cortex development), and in the proximal immature areas (ChP root) calbindin and PCNA related to progenitor activity and proliferation.