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Untitled - D Ank Unlimited

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ulcerative colitis (immunologic colitis) 732 ungulate immunity<br />

activated T cells but only a proportion of resting T cells.<br />

This antibody and antibodies to the high molecular-weight<br />

form of CD45 (CD45R) seem to define complementary,<br />

largely nonoverlapping populations in resting peripheral<br />

T cells demonstrating heterogeneity within the CD4 and<br />

CD8 subsets. The antibody labels most thymocytes, a<br />

subpopulation of resting T cells within both the CD4 and<br />

CD8 subsets, and mature activated T cells. Cells of the<br />

myelomonocytic series (e.g., granulocytes and monocytes)<br />

are also labeled, whereas most normal B and natural killer<br />

(NK) cells are consistently negative. Weak cytoplasmic<br />

staining is, however, seen in cases of centroblastic and<br />

immunoblastic lymphoma.<br />

Ulcerative colitis; crypt abscess.<br />

ulcerative colitis (immunologic colitis)<br />

An ulcerative condition that may involve the entire colon<br />

but does not significantly affect the small intestine.<br />

Neutrophils, plasma cells, and eosinophils infiltrate the<br />

colonic mucosa, followed by ulceration of the surface epithelium,<br />

loss of goblet cells, and formation of crypt abscess.<br />

The etiology is unknown. An immune effector mechanism<br />

is believed to maintain chronic disease. Serum immunoglobulins<br />

and peripheral blood lymphocyte counts are<br />

usually normal. Complexes present in the blood are relatively<br />

small and contain IgG, although no antigen has been<br />

identified. The complexes may be merely aggregates of<br />

immunoglobulin G (IgG). Patients have diarrhea with blood<br />

and mucus in stools. The signs and symptoms are intermittent,<br />

and the severity of colon lesions varies. Lymphocytes<br />

are cytotoxic for colon epithelial cells. Antibodies against<br />

Escherichia coli may cross react with colonic epithelium;<br />

whether such antibodies play a role in etiology and pathogenesis<br />

remains to be proven.<br />

ultracentrifugation<br />

The separation of cell components, including organelles<br />

and molecules, through high-speed centrifugation reaching<br />

6000 rpm with a gravitational force of up to 500,000 g. In<br />

differential velocity centrifugation, a stepwise increase in<br />

gravitational force removes selected components. Following<br />

centrifugation of a cellular homogenate at 600 g for 10<br />

minutes to isolate the nuclei, further spinning at 15,000<br />

g for 5 minutes permits isolation of mitochondria, lysosomes,<br />

and peroxisomes. Respinning at 100,000 g for 1<br />

hour permits isolation through sedimentation of the plasma<br />

membrane, microsomal fraction, endoplasmic reticulum,<br />

and large polyribosomes. Respinning at 300,000 g for 2<br />

hours permits sedimentation of ribosomal subunits and<br />

small polyribosomes. This leaves the cytosol—the soluble<br />

portion of the cytoplasm. Separation can also be achieved<br />

by sucrose density gradient ultracentrifugation. Combining<br />

cesium chloride with the molecules to be analyzed permits<br />

the molecules to migrate to a particular density equivalent.<br />

Ultracentrifugation may function as an analytical method<br />

for identifying proteins that differ in sedimentation coefficient<br />

or as a preparative method to separate proteins based<br />

on their densities and shapes.<br />

ultrafiltration<br />

The passage of solutions or suspensions through membranes<br />

with minute pores of graded sizes.<br />

umbrella effect<br />

The masking, by relatively large amounts of immunoglobulin<br />

G (IgG), of low immunoglobulin light chain concentrations<br />

in early IgM macroglobulinemia and IgA myeloma,<br />

observed in immunoelectrophoresis. Immunofixation<br />

electrophoresis, employing fluorochrome-labeled antibodies,<br />

can resolve this masking effect.<br />

undifferentiated connective tissue disease<br />

A prodromal phase of a collagen vascular or connective<br />

tissue disease during which the principal clinical manifestations<br />

have not yet become apparent.<br />

Ungulate immunity.<br />

ungulate immunity<br />

Ungulates develop immune systems similar to those of<br />

most other mammalian species. The thymus and bone<br />

marrow serve as the sources for generation of T and B<br />

cells, respectively. A feature unique to ruminant ungulates<br />

is the major role played in primary B cell development by<br />

the ileal Peyer’s patch, which is a single structure in the<br />

terminal ileum. Ruminants have a higher proportion of<br />

γδ T cells than other species. Ungulate immunoglobulins<br />

consist of IgG 1, IgG 2, IgM, IgA (serum), IgA (secretory),<br />

and IgE isotypes. IgA antibodies predominate on mucosal<br />

surfaces; mammary glands produce milk that is different<br />

in immunoglobulin content compared to other species. No

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