The embryonic blood- cerebrospinal fluid barrier function before the formation of the fetal choroid plexus: role in cerebrospinal fluid formation and homeostasis CEREBROSPINAL FLUID PHYSIOLOGY AND MOVEMENT
نویسندگان
چکیده
www.cmj.hr Cerebrospinal fluid (CSF) has attracted interest as an active signaling milieu that regulates brain development, homeostasis, and course disease. CSF is a nutrient-rich fluid, which also contains growth factors and signaling molecules that regulate multiple cell functions in the central nervous system (CNS). CSF constitution is controlled tightly and constituent concentrations are maintained narrow, depending on developmental stage. From fetal stages to adult life, CSF is produced mainly by the choroid plexus. The development and functional activities of the choroid plexus, and other blood-brain barrier systems in adults, have been extensively analyzed. However, the study of CSF production and homeostasis in embryos from the closure of the anterior neuropore, when the brain cavities become physiologically sealed, to the formation of the functional fetal choroid plexus has been largely neglected. This developmental stage is characterized by tightly controlled morphological and cellular events in the anterior part of the CNS, such as rapid brain anlagen growth and initiation of primary neurogenesis in the neural progenitor cells lining the cavities, events which are driven by specific molecules contained within the embryonic CSF. In this article, we review the existing literature on formation and function of the temporary embryonic blood-CSF barrier, from closure of the anterior neuropore to the formation of functional fetal choroid plexuses, with regard to crucial roles that embryonic CSF plays in neural development. David Bueno, Maryam Parvas, Jordi GarciaFernàndez
منابع مشابه
Cerebrospinal fluid physiology of the developing fetus.
Formation of the ventricular system begins at the time the neural groove closes to form a neural tube. Fluid is present within the tube, even before the choroid plexus anlage appears. This fluid serves as a structural support for the tube, as well as a pathway for diffusion of metabolites prior to the formation of blood vessels. In the small, thin-walled fetal brain, fluid movement is character...
متن کاملBicarbonate formation in cerebrospinal fluid: role in sodium transport and pH regulation.
MAREN, THOMAS H. Bicarbonate formation in cetebrospinal fluid: role in sodium transport and pH regulation. Am. J. Physiol. 222(4) : 885-899. 1972.-Two series of experiments were performed which clarified the role of HCOaformation and movement into cerebrospinal fluid (CSF), and its relation to sodium transport and pH regulation. In the first, the rates of access of HC03, Na+, and Clfrom plasma ...
متن کاملA SCL4A10 gene product maps selectively to the basolateral plasma membrane of choroid plexus epithelial cells.
The choroid plexus epithelium of the brain ventricular system produces the majority of the cerebrospinal fluid and thereby defines the ionic composition of the interstitial fluid in the brain. The transepithelial movement of Na+ and water in the choroid plexus depend on a yet-unidentified basolateral stilbene-sensitive Na+-HCO3- uptake protein. Reverse transcriptase-polymerase chain reaction (R...
متن کاملReassessing cerebrospinal fluid (CSF) hydrodynamics: a literature review presenting a novel hypothesis for CSF physiology.
The traditional model of cerebrospinal fluid (CSF) hydrodynamics is being increasingly challenged in view of recent scientific evidences. The established model presumes that CSF is primarily produced in the choroid plexuses (CP), then flows from the ventricles to the subarachnoid spaces, and is mainly reabsorbed into arachnoid villi (AV). This model is seemingly based on faulty research and mis...
متن کاملAltered pHi regulation and Na /HCO3 transporter activity in choroid plexus of cilia-defective Tg737 mutant mouse
Banizs B, Komlosi P, Bevensee MO, Schwiebert EM, Bell PD, Yoder BK. Altered pHi regulation and Na /HCO3 transporter activity in choroid plexus of cilia-defective Tg737 mutant mouse. Am J Physiol Cell Physiol 292: C1409–C1416, 2007. First published December 20, 2006; doi:10.1152/ajpcell.00408.2006.—Tg737 mice have defects in cilia assembly and develop hydrocephalus in the perinatal period of lif...
متن کامل