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Biomedical subjects

K Bill

Publications and source records attributed to K Bill.

18 recordsLinked to original sources

Novel C5a receptor antagonists regulate neutrophil functions in vitro and in vivo.

Novel recombinant human C5a receptor antagonists were discovered through modification of the C terminus of C5a. The C5a1-71T1M,C27S,Q71C monomer, (C5aRAM; CGS 27913), was a pure and potent functional antagonist. The importance of a C-terminal cysteine at position 71 to antagonist properties of C5aRAM was confirmed by studying C5a1-71 derivatives with replacements of Q71, C5a derivatives of various lengths (70-74) with C-terminal cysteines, and C5a derivatives of various lengths (71-74) with Q71C replacements. The majority of C5a1-71Q71 derivatives were agonists (C5a-like) in the human neutrophil C5a-induced intracellular calcium mobilization assay. The C5a1-71Q71C derivative was an antagonist. C5a derivatives of lengths 73 and 74 with C-terminal cysteines were agonists, while lengths 70 to 72 were antagonists. C5a derivatives of lengths 72, 73, and 74 with Q71C replacements were agonists, while, again, C5a1-71Q71C was an antagonist. C5aRAM and its adducts, including its dimer, C5aRAD (CGS 32359), were pure antagonists. Additionally, CSaRAM and CSaRAD inhibited binding of 125I-labeled recombinant human C5a to neutrophil membranes (Ki = 79 and 2 pM, respectively), C5a-stimulated neutrophil intracellular calcium mobilization (8 and 13 nM), CD11b integrin up-regulation (10 and 1 nM), superoxide generation (182 and 282 nM), lysozyme release (1 and 2 microM), and chemotaxis (11 and 7 microM). In vivo, intradermal injection of C5aRAM inhibited C5a-induced dermal edema in rabbits. Furthermore, a 5-mg/kg i.v. bolus of C5aRAD significantly inhibited C5a-induced neutropenia in micropigs when challenged with C5a 30 min after C5aRAD administration. C5aRAM and C5aRAD are novel, potent C5a receptor antagonists devoid of agonist or proinflammatory activity with demonstrated efficacy in vitro and in vivo.

Animals↗

Interaction of reduced and oxidized cytochrome c with the mitochondrial cytochrome c oxidase and bc1-complex.

Making use of a hetero-bifunctional reagent (succinimidyl 4-(p-male-imidophenyl)butyrate, SMPB), yeast cytochrome c was linked through a thioether bond to the maleimide group whereas the active N-hydroxy-succinimide ester site of the SMPB was used for the reaction with the primary amino groups of Affi-gel 102. The capacity and stability (also to reducing agents) of the column were greatly improved relative to previous systems. This new gel allowed the study of the interactions of cytochrome c oxidase and reductase with reduced and oxidized cytochrome c. For cytochrome c oxidase a significant difference in the interaction with ferri- and ferro-cytochrome c was observed but no such a difference was seen in the case of cytochrome c reductase.

Animals↗

Affinity chromatography purification of cytochrome c oxidase and b-c1 complex from beef heart mitochondria. Use of thiol-sepharose-bound Saccharomyces cerevisiae cytochrome c.

A method for simultaneous purification of cytochrome c reductase and cytochrome c oxidase using a cytochrome c affinity column is presented. Cytochrome c from Saccharomyces cerevisiae was linked to an activated thiol-Sepharose gel via its Cys-102 residue located far from the lysine residues on the front side of the molecule, responsible for the interaction with the reductase and oxidase. In previously reported affinity chromatography techniques these lysine residues most probably reacted with the column. Cytochrome c oxidase and reductase from bovine heart mitochondria bind specifically to the affinity column and can be recovered separately at different ionic strength in the elution buffer. The enzymes are highly pure and active.

Animals↗

Affinity chromatography purification of cytochrome c binding enzymes.

An efficient affinity chromatography procedure for the isolation of mitochondrial cytochrome c oxidase and reductase is described. Saccharomyces cerevisiae cytochrome c was used as a ligand, bound to a thiol-Sepharose 4B gel through cysteine-107. In this way, the site of interaction of cytochrome c with cytochrome oxidase and reductase remained unmodified and available for binding to a number of partner enzymes. The procedure is adequate for the purification of all those proteins having in common the property of binding with high affinity to cytochrome c--e.g., cytochrome c oxidase, reductase, and peroxidase, sulfite oxidase, and reaction centers of photosynthetic bacteria.

Animals↗

Human milk banking. Effect of refrigeration on cellular components.

The storage of human milk at 4 C for 48 hours after expression resulted in a significant (p < 0.02) loss of cellular viability. Further, the concentration of milk macrophages and neutrophils decreased significantly (p < 0.02), presumably via cell adhesion to the milk container or cytolysis. The milk lymphocyte concentration, however, was not significantly affected by storage. Milk passage through a nasogastric feeding catheter had no additional effect on cell viability or concentration. Thus, while current banking methodologies allow greater availability of breast milk's resistance factors to newborn infants, they do so with significant, but not serious, alterations in both the quantity and quality of these components.

Humans↗

Immunoglobulin synthesis by cord blood lymphocytes.

The IgG, IgA and IgM synthesis by adult peripheral blood and cord blood lymphocytes incubated alone and with pokeweed mitogen was quantitated. The cord blood lymphocytes produced no immunoglobulin even with mitogen stimulation while the adult peripheral blood lymphocytes responded to the mitogen with a significant (p less than 0.04) increase in immunoglobulin production.

Adult↗

Diagnosis of gangrene and perforation of the gallbladder by endoscopic retrograde cholangiography.

Conventional radiographic procedures are not helpful in the preoperative documentation of gangrenous cholecystitis or gallbladder perforation. Three cases in which preoperative diagnosis was accomplished by endoscopic retrograde cholangiography are described. Gangrene was identified in all three by a shaggy outline of the gallbladder wall with amorphous debris and stones in the lumen. Perforation was identified in two of the cases by extravasation of contrast material into a pericholecystic abscess. This information, as well as the status of the common duct, was important to the surgeon.

Cholangiography↗

Fusion anomalies of the pancreatic ductal system differentiation from pathologic states.

If fusion of the ventral and dorsal pancreatic ducts does not occur during fetal life, endoscopic retrograde cannulation of the papilla of Vater will visualize a small complete ductal system which is confined to the head of the pancreas. This system is characterized by normal arborizations throughout, relatively small duct diameters and the absence of a communication with the minor papilla. In contrast, if fusion has taken place and the ductal system is shortened by disease, pancreatography will demonstrate abrupt proximal termination or proximal tapering without side branches, and may show a significant duct of Santorini. If the ducts have fused, an area of narrowing approximately 3-20 mm in length commonly occurs at the level of fusion. This should not be confused with pathologic ductal stenosis.

Diagnosis, Differential↗

The importance of mouth care.

Practice profiles are reflective pieces written by nurses in practice, and based on continuing professional development articles. This week Karen Bill discusses the importance of mouth care.

Attitude of Health Personnel↗