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Biomedical subjects

M Hornung

Publications and source records attributed to M Hornung.

25 records · Page 2Linked to original sources
PubMed1987

[Postoperative endotoxin determination and immunoglobulin therapy of infected patients in the intensive care unit].

Seventy-four patients with septic postoperative complications were prospectively listed. Plasma-borne endotoxin was daily determined in all of them by means of the limulus-amoebocyte-lysate test. Maximum sensitivity of the test amounted to 64 per cent, related to days of illness due to severe septicaemia. The conclusion is drawn that additional parameters should be used in future studies to define sepsis, including determination of sepsis score. Endotoxin titres declined in response to immunoglobulin therapy. Lethality went down, as well.

Adolescent↗
PubMed1979

[Proof of glycosaminoglycans in the corneal endothelium].

The corneal endothelium of three species (man, dog, and guinea pig) was examined for glycosaminoglycans by using TEM, REM, and EDAX (energy-dispersive analysis of X-rays). Since no clear results can be determined by using ruthenium red (RR) alone, a testicular hyaluronidase was used to digest the glycocalyx. After incubation with hyaluronidase, the dark RR borderline of the outer leaflet of the cell membrane became more fluffy when examined by using TEM and REM. When EDAX was applied, the Ru peak became smaller compared with the S peak. These impressive results had not been found when the material was fixed in glutaraldehyde for 24 h before incubation. Considering the individual results, it can be concluded that RR, even wouthout OsO4, marks the acid groups of glycosaminoglycans that might be in the cell membrane, as well as other acid groups. There was no difference in the results among the three species used in this experiment. Some pictures showed that RR/OsO4 penetrates through the intercellular space into the Descemet's membrane.

Animals↗
PubMedDate not supplied

Preferential migration of CD62L cells into the appendix in mice with experimental chronic colitis.

BACKGROUND: Clinical and experimental studies suggest that appendectomy can protect against development of ulcerative colitis and Crohn's disease. However, how T cells in the appendix affect the development of colitis has not been clarified. AIM: To investigate the in vivo migration and activation of colitis-inducing CD62L+ cells during development of chronic colitis. METHODS: CD62L+CD4+ cells were fluorescently labeled and transferred to severe combined immunodeficient (SCID) mice to induce colitis. In vivo migration of T cells into the mucosa of the appendix and colon was quantified by in vivo microscopy after 7 weeks. In a second experiment, unlabeled CD62L+CD4+ cells were transferred, reisolated after 7 weeks, and adhesion molecule (integrin alpha4beta7) and costimulatory molecule (CD154) expression was analyzed. RESULTS: Six to eight weeks after CD62L+CD4+ cell transfer, SCID mice developed chronic colitis. In vivo microscopic analysis demonstrated a preferential migration of fluorescence-labeled CD62L+CD4+ cells into the mucosa of the appendix versus the colon. Re-isolation of lamina propria cells from mice with colitis confirmed that CD62L+CD4+ cell migration was significantly enhanced in the appendix, compared to the colon (3.5-fold). Furthermore, a higher proportion of CD62L+CD4+ cells re-isolated from the appendix expressed integrin alpha4beta7 and CD154 than from the colon. CONCLUSION: This study demonstrates the preferential migration of CD62L+CD4+ cells into the appendix as compared to the colon. This migration pattern correlated with upregulation of integrin alpha4beta7 and CD154 (CD40 ligand) on T cells. Our results suggest an important role of the appendix in the pathogenesis of colitis.

Adoptive Transfer↗