Biomedical subjects

K Warfvinge

Publications and source records attributed to K Warfvinge.

21 records · Page 2Linked to original sources

PubMed1988

Single modified cilia displayed by cells of human internal stratified epithelia (oral cavity, vagina).

Serial sections of human vaginal and keratinized oral-gingival epithelia were investigated for ciliary structures. Most melanocytes of the gingival epithelium lacked cilia, whereas almost all basal keratinocytes of the deeper portion of the epithelial ridges possessed one cilium each. In the suprabasal layers of the ridges only a few keratinocytes exhibited a single cilium. In the basal layer, at the top of the connective tissue papillae, approximately every second keratinocyte displayed a single cilium. In the suprabasal layers above the ridges no ciliated keratinocytes were observed. The basal cells of the vaginal epithelium were endowed with cilia, while cilia were absent from the suprabasal cells. In the human forearm epidermis most melanocytes and keratinocytes are supplied with a single cilium; it has been suggested that they may play a role in light reception. However, the widespread occurrence of 9 + 0 cilia in epithelial cells of internal epithelia and their coincidence with the sites of renewal of keratinocytes suggests that a relationship may exist between solitary cilia and mitotic activity.

Adult↗

PubMed1987

New views on the construction of human gingival epithelium.

The effects on the basal and spinous layers of human keratinized oral epithelium of 2 glutaraldehyde-based fixatives with buffers hypoosmolar and isoosmolar to blood, respectively, have been investigated. The first-mentioned solution produced an electron microscopic image corresponding to the classical view, that is an epithelium consisting of closely-packed cells having short and stubby membrane projections and separated by an extremely narrow intercellular space. In the Langerhans cells, the specific granules appeared racket-shaped and had a unilaminar limiting membrane with a periodic structure along its internal face. There are strong reasons to believe that these morphological characteristics are swelling artifacts. The last-mentioned fixative produced keratinocytes provided with numerous microvilli and membrane ruffles and disk-shaped Langerhans cell granules surrounded by a trilaminar membrane. Concomitantly, the intercellular space appears very wide and there is evidence for the view that this is a more realistic picture of the in vivo situation and not a gross distortion caused by shrinking during the tissue processing. Broad interstices can explain certain basic events as rapid cell motility within the epithelium and offer efficient pathways for rapid transport of substances.

Adult↗

PubMedDate not supplied

Expression of nitric oxide synthase during the development of RCS rat retinas.

Nitric oxide (NO) has been reported to be both neurodestructive and neuroprotective in the central nervous system and could possibly play an important role in neurodegenerative disorders. On the assumption that NO synthesis may influence degenerative processes in the retina, we have examined the development and distribution of nitric-oxide-synthase(NOS)-immunoreactive cells in developing Royal College of Surgeons (RCS) rat retinas, which is an animal model for retinal degeneration. An antibody against constitutive neuronal NOS was used for immunocytochemistry on RCS rat retinas from postnatal (PN) days 3, 7, 10, 14, 35, 70 and 281 and compared with that in the normal rats of PN days 3, 7, 10, 14, 54 and adults. Immunoreactive cells were not seen in PN 3 retinas but were distinctly seen in the PN 7 retina along with a plexus in the inner plexiform layer. In both groups (normal and RCS rats) a distinct sublayering of the plexus in the inner plexiform layer could be seen at PN 10, which became more distinct at PN 14. The immunoreactive cells were detected also in the oldest retina examined, which was PN 281 in the case of RCS rats. In both groups, certain amacrine cells, certain bipolar cells and certain horizontal cells were found to be immunoreactive. In conclusion, the developmental timetable of the NOS immunoreactivity was identical in the normal and the RCS rat retinas. The NOS-immunoreactive cells persisted in the RCS retinas even when the retina had degenerated extensively. Abnormalities with the inducible isoforms of NOS cannot be ruled out from this study. We conclude that the chronological and qualitative development of the constitutive neuronal NOS immunoreactivity is normal in RCS rat retinas.

Animals↗