Table 2.
WPC | Feature | Species | References |
---|---|---|---|
6th | Appearance of a primary meninx around most parts of the brain | Human | O'Rahilly and Muller, 1986 |
Amoeboid microglial cells penetrate the brain by crossing the pial basement membrane | Human | Verney et al., 2010 | |
7th | The skeletogenous layer becomes visible | Human | O'Rahilly and Muller, 1986 |
Differentiation of a leptomeningeal meshwork that is presumed to contain liquid and represent the future SAS | Human | O'Rahilly and Muller, 1986 | |
8th | The dural limiting layer is almost complete in hindbrain and midbrain but only present in the area adjacent to the lateral fossa in the forebrain | Human | O'Rahilly and Muller, 1986 |
The fenestrated sinusoids of the pia-arachnoid become non-fenestrated (E14) | Rat (E14) | Balslev et al., 1997 | |
Most of the cisternae of the adult is already present | Human | O'Rahilly and Muller, 1986 | |
7–10th | Initial communication between the ventricular and subarachnoid compartments | Human and rat (E17) | Brocklehurst, 1969; Johansson et al., 2008 |
11th | Completion of the subpial end feet layer (E16) and claudin-11 positive arachnoid blood-CSF barrier (E18) and thereby appearance of a clearly defined subarachnoid space | Rat (E16 and E18) | Balslev et al., 1997 |
12–13th | Second wave of microglial cells penetrate the brain via the BBB and inner CSF-brain barrier | Human | Verney et al., 2010 |
12 (13–15th) | RGCs begin to transform into astrocytes | Rhesus monkey (E64) and newborn ferret | Schmechel and Rakic, 1979; Voigt, 1989 |
25–28th | Transition from subpial end feet layer to glia limitans | Human | Kadhim et al., 1988 |
Data were mainly based on human material and approximated to weeks post-conception. It is clearly stated when results from other mammals are used. The work of Clancy et al. (2001) was used for conversion to estimated human age.