Human subcommissural organ, with particular emphasis on its secretory activity during the fetal life

The subcommissural organ (SCO) is a conserved brain gland present throughout the vertebrate phylum. During ontogeny, it is the first secretory structure of the brain to differentiate. In the human, the SCO can be morphologically distinguished in 7‐ to 8‐week‐old embryos. The SCO of 3‐ to 5‐month‐old fetuses is an active, secretory structure of the brain. However, already in 9‐month‐old fetuses, the regressive development of the SCO‐parenchyma is evident. In 1‐year‐old infants, the height of the secretory ependymal cells is distinctly reduced and they are grouped in the form of islets that alternate with cuboid non‐secretory ependyma. The regression of the SCO continues during childhood, so that at the ninth year of life the specific secretory parenchyma is confined to a few islets of secretory ependymal cells. The human fetal SCO shares the distinct ultrastructural features characterizing the SCO of all other species, namely, a well‐developed rough endoplasmic reticulum, with many of its cisternae being dilated and filled with a filamentous material, several Golgi complexes, and secretory granules of variable size, shape, and electron density. The human fetal SCO does not immunoreact with any of the numerous polyclonal and monoclonal antibodies raised against RF‐glycoproteins of animal origin. This and the absence of RF in the human led to the conclusion that the human SCO does not secrete RF‐glycoproteins. Taking into account the ultrastructural, lectin‐histochemical, and immunocytochemical findings, it can be concluded that the human SCO, and most likely the SCO of the anthropoid apes, secrete glyco‐ protein(s) with a protein backbone of unknown nature, and with a carbohydrate chain similar or identical to that of RF‐glycoproteins secreted by the SCO of all other species. These, as yet unidentified, glycoprotein(s) do not aggregate but become soluble in the CSF. Evidence is presented that these CSF‐soluble proteins secreted by the human SCO correspond to (1) a 45‐kDa compound similar or identical to transthyretin and, (2) a protein of about 500 kDa. Microsc. Res. Tech. 52:573–590, 2001. © 2001 Wiley‐Liss, Inc.

[1]  B. Dastugue,et al.  SCO-spondin is evolutionarily conserved in the central nervous system of the chordate phylum , 1999, Neuroscience.

[2]  E. Rodríguez,et al.  Partial sequencing of Reissner’s fiber glycoprotein I (RF-Gly I) , 1998, Cell and Tissue Research.

[3]  E. Rodríguez,et al.  The subcommissural organ , 1998, Microscopy research and technique.

[4]  M. Cifuentes,et al.  Bovine Reissner’s fiber (RF) and the central canal of the spinal cord: an immunocytochemical study using a set of monoclonal antibodies against the RF-glycoproteins , 1996, Cell and Tissue Research.

[5]  E. Rodríguez,et al.  Immunochemical analysis of the subcommissural organ-Reissner’s fiber complex using antibodies against alkylated and deglycosylated glycoproteins of the bovine Reissner’s fiber , 1996, Cell and Tissue Research.

[6]  B. Dastugue,et al.  SCO-spondin: a new member of the thrombospondin family secreted by the subcommissural organ is a candidate in the modulation of neuronal aggregation. , 1996, Journal of cell science.

[7]  E. Rodríguez,et al.  Historical Landmarks in the Investigation of the Subcommissural Organ and Reissner’s Fiber , 1993 .

[8]  E. Rodríguez,et al.  Evidence for the Release of CSF-Soluble Secretory Material from the Subcommissural Organ, with Particular Reference to the Situation in the Human , 1993 .

[9]  A. Oksche Phylogenetic and Conceptual Aspects of the Subcommissural Organ , 1993 .

[10]  R. Olsson Reissner’s Fiber Mechanisms: Some Common Denominators , 1993 .

[11]  E. Rodríguez,et al.  Cell biology of the subcommissural organ. , 1992, International review of cytology.

[12]  E. Rodríguez,et al.  Identification and partial characterization of the secretory glycoproteins of the bovine subcommissural organ-Reissner's fiber complex. Evidence for the existence of two precursor forms. , 1991, Brain research. Molecular brain research.

[13]  W. Naumann [Immunohistochemical investigations on the ontogenesis of the subcommissural organ]. , 1986, Acta histochemica. Supplementband.

[14]  A. Castañeyra-Perdomo,et al.  The early development of the human subcommissural organ. , 1985, Journal of anatomy.

[15]  C. Bouchaud,et al.  The ependymal secretion of the fetal and adult rat subcommissural organ. morphological aspects linked to the synthesis, storage and release of the secretory products , 1983, Biology of the cell.

[16]  T. Shimada,et al.  The fine structure of the subcommissural organ of the human fetus. , 1970, Archivum histologicum Japonicum = Nihon soshikigaku kiroku.

[17]  U. Smith Aspects of fine structure and function of the subcommissural organ of the embryonic chick. , 1970, Tissue & cell.

[18]  M. Palkovits,et al.  [Topographical relations of the human subcommissural organ to the epiphysis and their functional significance]. , 1962, Endokrinologie.

[19]  R. Olsson Subcommissural ependyma and pineal organ development in human fetuses. , 1961, General and comparative endocrinology.

[20]  R. Friede Surface structures of the aqueduct and the ventricular walls: α Morphologic, comparative and histochemical study , 1961, The Journal of comparative neurology.

[21]  P. Gõmez Bosque,et al.  The subcommissural organ in the grown-up man. , 1961, Acta anatomica.

[22]  G. B. Wislocki,et al.  Selective staining of the human subcommissural organ , 1958, The Anatomical record.

[23]  W. Möllendorff,et al.  Handbuch der Mikroskopischen Anatomie des Menschen , 1958 .

[24]  Keene Mf,et al.  The Subcommissural Organ and the Mesocoelic Recess in the Human Brain, together with a note on Reissner's Fibre. , 1935 .

[25]  A. Opalski Über lokale Unterschiede im Bau der Ventrikelwände beim Menschen , 1934 .