Porcine choroid plexus cells in culture: expression of polarized phenotype, maintenance of barrier properties and apical secretion of CSF-components.

We have successfully cultured choroid plexus epithelial cells from porcine brain in pure form by the addition of cytosine arabinoside to the culture medium which prevented growth of other contaminating cells. We characterized the cells in culture by the presence of desmoplakin, fibronectin, thrombospondin, and the zonula occludens protein ZO-1 in comparison to frozen fractions of the isolated choroid plexus tissue. The cells in culture express those marker proteins and moreover exhibit a polarized phenotype which was expected from the presence of tight junction strands that correlate to an electrical resistance of 120 Ohm.cm2 measured across the cell monolayer on a permeable support. Permeability studies with fluorescein-labeled dextrans also indicate a biochemical tightness. The polarity of the cells is demonstrated by the presence of microvilli and cilia on the surface of the cultured cells as well as by the laser scanning microscopic determination of the apical localization of the ZO-1-protein and the Na+K(+)-ATPase. Thrombospondin and fibronectin were found to be localized at the basolateral membrane side. The cells in culture secrete medium containing prealbumin predominantly into the apical compartment which demonstrates that they are able to release medium containing CSF-proteins and therefore verifies the usefulness of this in vitro model.

Constitutive secretion of beta-trace protein by cultivated porcine choroid plexus epithelial cells: elucidation of its complete amino acid and cDNA sequences.

Primary porcine choroid plexus epithelial cells cultivated in chemically defined medium maintain their epithelial characteristics and form confluent monolayers. They produce a fluid the composition of which resembles cerebrospinal fluid. The present study demonstrates constitutive secretion of large amounts of beta-trace protein. This intrathecally synthesized protein is a prominent polypeptide constituent of natural cerebrospinal fluid. According to the identity of amino acid sequences it has previously been tentatively identified as a prostaglandin-D synthase and as a member of the lipocalin protein family. beta-Trace was purified from cell culture supernatants and was subjected to tryptic digestion and amino acid sequencing of the resulting peptides. The complete primary structure of the protein was obtained by additional isolation of the cDNA from cultured epithelial cells. The porcine 163-amino acid polypeptide showed 69% identity with the human beta-trace and contained two N-glycosylation sites occupied by complex-type oligosaccharides as is the case for the human protein. The amino acid sequences around the N-glycosylation sites of mammalian beta-trace proteins (porcine, human, murine, and rat) were highly conserved. The nucleotide sequence was found to be less conserved; the porcine cDNA had a strikingly high GC-content (67%). The constitutive secretion of beta-trace protein from the in vitro cultivated porcine choroid plexus epithelial cells demonstrates that the cells have retained their major in vivo physiological properties: secretion of cerebrospinal fluid proteins. Therefore, this in vitro culture system may be used as a versatile tool for studying the regulation of the formation of cerebrospinal fluid.

Biochemical and histological study of the ossification in the early developing pedicle of the fallow deer (Dama dama).

To date, no histochemical data exist concerning the process of ossification of developing pedicles in deer. Four different zones of the growing pedicle (subcutaneous tissue; fibrous layer of the periosteum; cambial layer of the periosteum; woven bone of the primary spongiosa) were analysed in direct correlation to their histological appearance. The level of extractable specific alkaline phosphatase in the preosseous zones of the pedicle was 4-fold higher than levels in the epiphyseal growth plate previously reported. These results reflect that rapid bone formation takes place in the growing pedicle. Highest buffer-extractable alkaline phosphatase activity was found in the cambial layer directly in front of the mineralization area of the pedicle-bone, connected with maximal values for organically bound phosphate and inorganic phosphate. Moreover, the values for buffer-extractable alkaline phosphatase, organically bound phosphate and inorganic phosphate decreased with increasing mineralization in the zone of the primary spongiosa. The present histological and biochemical findings on the process of ossification in the pedicle show similarities to typical endochondral ossification. The process of pedicle growth may serve as a new and important system for chondrogenic and osteogenic studies, including a better understanding of antler development.

Light microscopic observations on the ossification process in the early developing pedicle of fallow deer (Dama dama).

The ossification process of the early developing pedicle was studied in five male fallow deer fawns, aged about seven months. The incipient pedicle was covered by a periosteum, the cambial layer of which was significantly thicker at the apex of the outgrowth than in the more peripheral areas of the pedicle. As was demonstrated histologically, in the central part of the pedicle elongation occurred by a process corresponding to endochondral ossification, whereas in the more peripheral areas the pedicle became enlarged by typical intramembranous ossification. Thus, cartilage formation must be regarded as a normal feature in pedicle growth of fallow deer. The assumption that the transition from pedicle to first antler growth in cervids is reflected by a switch from intramembranous ossification to chondrogenesis at the apex of the growing primary cranial appendage, based mainly on observations in roe deer, does, therefore, not hold for fallow deer. Furthermore, histogenesis of the central part of the fallow deer pedicle closely resembles the developmental events leading to formation of subsequent antlers.