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W R Hein

Publications and source records attributed to W R Hein.

At least 55 records · Page 3Linked to original sources
PubMed1991

Expression of the "T19" and "null cell" markers on gamma delta T cells of the sheep.

A 215 kDa molecule termed T19 marks CD4-CD8- T cells in sheep and cattle. In this report, we analysed the T19 or "null cell" panel of mAbs against gamma delta T cells of sheep, using a mAb specific for the gamma delta TCR. By two-colour immunofluorescence, all of the mAbs in the T19 panel reacted with gamma delta T cells or subsets thereof, although staining intensities and percentages of cells stained by the different mAbs indicated considerable heterogeneity for the T19 molecule. This probably results from differential expression of certain epitopes on T19. The reactivity of most of the mAbs for the 215 kDa T19 molecule was also confirmed by immunoprecipitation and SDS-PAGE.

Animals↗
PubMed1991

Prominence of gamma delta T cells in the ruminant immune system.

The lymphoid systems of sheep and cattle contain a large number of gamma delta T cells, in striking contrast to the lymphoid systems of humans and mice. In neonatal animals particularly, these cells comprise the predominant fraction of T cells in the blood. Here Wayne Hein and Charles Mackay discuss what is currently known about the ontogeny, phenotype, tissue distribution and function of gamma delta T cells in ruminants. There are a number of interesting molecular features that characterize ruminant gamma delta T cells, but these do not entirely explain the high frequency of use of the gamma delta T-cell receptor in these animals. Studies on sheep, cattle or other animals that preferentially use gamma delta T cells should provide insights into the biological significance of the existence of two distinct forms of the T-cell receptor.

Animals↗
PubMed1991

Mixed micelles as a proliposomal, lymphotropic drug carrier.

Four lipophilic, low molecular weight drugs solubilized in phosphatidylcholine-bile salt mixed micelles were injected s.c. into the hind legs of sheep and their cumulative recoveries in lymph draining from the site of application were determined. Surprisingly, the cumulative recoveries (percentage of dose) varied between less than 1 and 60%. We found that there is a correlation between the lipophilicity of the drug (log P octanol/water approximately Rm degrees value) and the proportion of the dose absorbed by the lymphatic route. Drugs with Rm degrees values greater than 10 are absorbed preferentially by the lymphatics (greater than 50% of dose), whereas compounds with Rm degrees values less than 4 are hardly absorbed at all by the lymphatics (less than 10% of dose). By applying the prodrug principle we demonstrated that it is also possible to target drugs with Rm degrees values less than 4 to the lymphatics. Furthermore, the analysis of the collected lymph samples by gel filtration, quasi-elastic light scattering, and electron microscopy revealed that, following s.c. administration, mixed micelles are converted into homogeneous, unilamellar vesicles. In conclusion, these results suggest that mixed micelles may represent a suitable delivery system for low molecular weight drugs whose targets are lymphoid cells. In addition, for drugs where liposomal application leads to a therapeutic advantage, the thermodynamically stable mixed micelle could be a good alternative to the liposome. However, for both applications a high drug lipophilicity is a prerequisite.

Absorption↗
PubMed1990

Characterization of the CD3 gamma and delta invariant subunits of the sheep T cell antigen receptor.

The CD3 gamma and delta chains of the sheep T cell antigen receptor have been characterized by cDNA cloning. In comparison to human and mouse protein sequences, short oligopeptide stretches have been deleted from both the gamma and delta chains. However, apart from further variability in the number and position of potential N-linked glycosylation sites, the general structure of the CD3 gamma and delta proteins is markedly conserved. Particularly remarkable are two motifs consisting of 8 and 32 amino acids, respectively, which locate in the C-terminal half of each protein and which have been precisely conserved in both the CD3 gamma and delta chains of all three species. These motifs probably contribute structural properties essential for the function of the CD3/T cell receptor complex. mRNA of the sheep CD3 gamma (1.5 and 1.2 kb) and CD3 delta (1.5 kb) chains are transcribed from closely linked, single-copy genes, suggesting that common mechanisms for the regulation of CD3 genes are also preserved between species.

Amino Acid Sequence↗
PubMed1990

Molecular cloning of sheep T cell receptor gamma and delta chain constant regions: unusual primary structure of gamma chain hinge segments.

The primary structure of sheep T cell receptor (TcR) gamma and delta chain constant (C) regions has been determined by cDNA cloning. A comparison of the nucleotide and deduced amino acid sequences of the sheep chains with known human and mouse sequences shows that the primary structure of the immunoglobulin, transmembrane and cytoplasmic C gamma domains and all of the C delta region has been substantially conserved. However, the hinge or connector region of sheep gamma chains differs significantly from all known TcR chains. Clones representing two different sheep C gamma genes were isolated and both contain additional sequence in this region, making them the longest TcR chains so far identified. The hinge region of both sheep C gamma sequences contains two additional cysteine residues and a motif of five amino acids (TTESP or TTEPP) which has been triplicated in one of the clones. Other repetitive segments of 13-17 amino acids could also be identified suggesting that, as in the human C gamma 2 gene, this region of the sheep genes could have arisen from an exon duplication or triplication event. Southern blot analysis of sheep DNA confirmed the presence of one C delta gene and at least two C gamma genes. A restriction fragment length polymorphism that is probably associated with allelic sequence variation in the sheep C delta gene was detected in DNA from different animals. Although the essential structure of the gamma/delta TcR appears well conserved through evolution, the marked heterogeneity evident in the hinge region of gamma chains both within and between species, and particularly the presence of additional cysteine residues in the sheep sequences, may be of structural and functional importance.

Amino Acid Sequence↗
PubMed1990

Differential peripheral expansion and in vivo antigen reactivity of alpha/beta and gamma/delta T cells emigrating from the early fetal lamb thymus.

The concentrations of different lymphocyte subsets in the blood of lambs which had been thymectomized (Tx) in utero between days 67-75 of fetal gestation were measured at birth and at various intervals during the first year of life. Compared to thymus-intact (Ti) controls, Tx lambs were severely depleted of both alpha/beta and gamma/delta T cells at birth (less than 10% of control levels). The majority of the residual alpha/beta T cells present in Tx lambs at birth were CD4+CD8-. As the Tx lambs aged, the concentration of alpha/beta T cells in blood increased steadily to reach levels around 50% of control values. In contrast, the circulating gamma/delta T cells did not expand in Tx animals and remained barely detectable throughout the observation period, although these cells accounted for 30%-60% of the T cells in the blood of Ti lambs. The expansion of alpha/beta but not gamma/delta T cells was also reflected in changes in the cellular composition of solid lymphoid organs in Tx lambs. B cell numbers were similar in both groups at birth but Tx lambs were persistently B lymphopenic from 3 weeks of age onwards. The alpha/beta T cells that had expanded in Tx lambs responded to stimulation with bacterial antigens in a way that was qualitatively similar to the response in Ti lambs. By contrast, the few gamma/delta T cells in Tx lambs responded abnormally. Our results show that although sheep alpha/beta and gamma/delta T cells are equally thymus dependent during ontogeny, the early fetal thymic emigrants which establish the two T cell lineages in the periphery have strikingly different antigen reactivities and capacities for self-renewal and expansion.

Aging↗
PubMed1990

Effect of molecular weight on the lymphatic absorption of water-soluble compounds following subcutaneous administration.

The lymphatic absorption of four water-soluble compounds with different molecular weights (MW) was determined by measuring their cumulative recovery in lymph draining from the site of s.c. administration in sheep. The cumulative recoveries (% of dose, mean +/- SD; N = 3) were 4.0 +/- 1.5 (5-fluoro-2'-deoxyuridine, MW 246.2), 21.0 +/- 7.1 (inulin, MW 5200), 38.6 +/- 6.7 (cytochrome c, MW 12,300), and 59.5 +/- 7.7 [human recombinant interferon (rIFN) alpha-2a, MW 19,000], respectively. Our data show that in the investigated MW range, there is a linear relationship between the molecular weight and the proportion of the dose absorbed lymphatically. An increase in molecular weight results in an increased lymphatic absorption. Molecules with MW greater than 16,000 are absorbed mainly by the lymphatics which drain the application site. The knowledge gained in this investigation may help to improve the mode of administration and therapeutic efficacy of endogenous proteins whose targets are lymphoid cells (e.g., interferons, interleukins). Practical implications for the clinical use of such proteins are discussed.

Absorption↗
PubMed1990

Distribution of lymphocyte subsets in the large intestinal lymphoid follicles of lambs.

The phenotypes of lymphocytes in the large intestinal patches (LIP) of lambs were examined by flow cytometry and immunohistology, using a panel of monoclonal antibodies (mAb), and compared to those found in the jejunal (JPP) and ileal Peyer's patches (IPP). T-cell markers were detected on 25% of the LIP and JPP lymphocytes by cytofluorometry, and nearly all T cells expressed the CD4 molecule. In contrast, T cells were scarce in the IPP (less than 1%). The B-cell marker p220 was expressed by 74% of the LIP lymphocytes, whereas surface immunoglobulin-positive cells comprised 50-60% of the lymphocyte population. The adhesion molecule CD2 was expressed by a larger proportion of cells from the LIP and JPP than from the IPP, whereas the adhesion molecule CD44 was detected on more IPP lymphocytes. Major histocompatibility complex (MHC) class I antigens were expressed by nearly all lymphocytes from the LIP, JPP and IPP. The LIP contained 70-80% cells with MHC class II expression, whereas the majority of IPP cells (greater than 95%) were MHC class II positive. Immunohistology showed many CD4+ T lymphocytes in the follicles of the LIP and JPP, but none in the IPP follicles. CD8+ lymphocytes were found in the interfollicular areas and were absent from the follicles. The interfollicular areas of the rectal patch contained about 15% tau delta T cells. In contrast, the JPP, IPP and the colon patch at the beginning of spiral colon contained less than 3% tau delta T cells.

Animals↗
PubMed1989

T cell receptor gene expression in sheep: differential usage of TcR1 in the periphery and thymus.

We have isolated cDNA clones for each chain of the sheep T cell receptor (TcR) and used these to analyze TcR gene expression in thymocyte and peripheral T cell subsets. Outer cortical thymocytes expressed a low level of mature message for all TcR chains suggesting that intrathymic precursors for the alpha/beta and gamma/delta lineages occur in this population. Inner cortical and medullary thymocytes expressed high levels of mature alpha/beta transcripts, low levels of mature delta transcripts but no detectable gamma message. Mature alpha/beta transcripts were detected in peripheral CD4+ lymphocytes and these as well as CD8+ cells expressed a surface heterodimer of 85 kDa which resolved into 40- and 50-kDa subunits after reduction. Peripheral CD4-CD8-lymphocytes, which in sheep are marked by the T19 antigen and may account for up to 60% of T cells in blood, expressed a surface heterodimer of 75 kDa. The T19+ cells had high levels of mature delta and truncated beta transcripts in their cytoplasm but did not express the C gamma gene detected in DN thymocytes, although they seem to share V gamma and/or J gamma elements. Both forms of the sheep TcR are associated with CD3 molecules on the cell surface. These results show that (a) in contrast to the situation in rodents and humans, a large proportion of peripheral sheep lymphocytes use TcR gamma/delta; (b) the proportion of T cells in the periphery which use TcR gamma/delta is greater than in thymus; and (c) CD4-CD8- cells in thymus and periphery (T19+) use the same C delta gene but appear to use different C gamma genes, suggesting that in sheep there may be more than one lineage of lymphocytes expressing TcR gamma/delta.

Animals↗
PubMed1989

Ontogeny, morphology and tissue distribution of a unique subset of CD4-CD8- sheep T lymphocytes.

The morphology, distribution and ontogeny of the 197+ T lymphocyte subpopulation is described. Cells were identified by immunofluorescent and immunoenzymic staining of cell suspensions and tissue sections. In the circulation, 197+ cells are small and regular, indistinguishable in size from peripheral CD4+ and CD8+ cells, with little cytoplasm and a large amount of condensed chromatin. In the post-natal animal they are unevenly distributed, being most common in the circulatory pathways, particularly in the blood. In the thymus they chiefly localize in the regions around Hassal's corpuscles and medullary blood vessels. They are totally absent from B cell areas in all tissues. They are the last of the T cells to appear in ontogeny, and are first detected in the thymus. Their frequency in blood is age-dependent with peak levels occurring perinatally. There is a post-natal decline in the frequency of 197+ cells in ileocaecal but not in prescapular lymph nodes. We conclude that these T cells differ from the more commonly described T cells, not only in their surface expression of the CD4, CD8 and T19 antigens, but also in the time of their first appearance, their age-related prevalence and their distribution between and within tissues.

Animals↗
PubMed1989

Functional characteristics of 197+ CD4- CD8- sheep T lymphocytes: expansion and differentiation of peripheral T cells.

This report describes the results of functional studies on the CD3+ 197+ CD4- CD8- TCR gamma/delta + peripheral T lymphocyte of sheep. Cell types were identified by immunofluorescent and immunoenzymic staining and separated by fluorescence activated flow cytometry. Newly synthesized DNA was labelled in vivo by incorporation of 5-bromo-2-deoxyuridine (BrdU), and total DNA by in vitro incubation with propidium iodide. Cells were challenged in vivo with alloantigens, in vitro with alloantigens or a range of mitogens, and activation/differentiation was assessed by determination of cell number, phenotype, and thymidine incorporation. In normal lambs the 197+ cells showed no in vivo DNA synthesis except at a low level in the ileocaecal lymph node. A similarly low level of synthesis in the prescapular node was induced by local allogeneic challenge. A higher proportion of 197+ cells than of other T cells isolated from blood and lymph had G2/M phase DNA content, while very few had S phase DNA content. The response of 197+ cells in terms of change in relative numbers following in vivo allogeneic challenge was quite different to that of CD4+ or CD8+ cells. Instead of rising to a peak at 5-8 days after challenge and then declining, the percentage of 197+ cells rose steadily with no evidence of decline by 14 days. Purified 197+ cells were activated in vitro by phytohaemagglutinin (PHA) and concanavalin-A (Con-A) but not by B cell mitogens; such activation was dependent on the inclusion of feeder cells or interleukin-2 (IL-2).(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1989

A large proportion of bovine T cells express the gamma delta T cell receptor and show a distinct tissue distribution and surface phenotype.

The numbers, phenotype, and tissue distribution of gamma delta T cells in cattle were studied using two monoclonal antibodies (mAbs) which react with the bovine gamma delta T cell receptor (TCR). Both mAbs stained 20-40% of T cells in peripheral blood, and immunoprecipitated molecules of 44 and 36 kd (reduced) and 70-80 kd (non-reduced). In cattle the majority of circulating gamma delta T cells showed a distinct surface phenotype; they expressed T19, a 215 kd molecule described in sheep and cattle which marks only gamma delta T cells. Bovine gamma delta T cells were also CD2-, CD4-, and mostly CD8-, and failed to express CD6, a molecule possibly involved in T cell activation. The distribution of gamma delta T cells in cattle lymphoid tissues differed markedly from that in humans, in that bovine gamma delta T cells were concentrated around lymph node trabeculae and were usually sparse or absent from the B cell and T cell domains of lymph nodes. Like most other species studied, gamma delta T cells in cattle were localized to epithelial surfaces, particularly within the skin and intestine, indicating that it was at these sites where gamma delta T cells functioned. Our results provide further evidence for the unusual localization, recirculation pattern, and phenotype of gamma delta T cells, and also show that some features of gamma delta T cells can differ quite markedly from species to species.

Animals↗
PubMed1989

Evidence that the B5 molecule on sheep lymphocytes is a homologue of mouse Ly 6 and human CD59.

When analysed by SDS-PAGE, the B5 molecule immunoprecipitated from sheep thymocytes, T cells and B cells migrated as multiple bands within a size range of 11,000-17,000 MW. After digestion with endoglycosidase-F, the precipitate from all cell types yielded a 6000 MW band. T-cell lysates gave an additional band at 6300 MW. All forms of the B5 molecule were anchored to the cell membrane via phosphatidylinositol. These results strengthen earlier evidence that the B5 molecule is a sheep homologue of the mouse Ly 6 antigen. The additional protein unit found on T cells may be of functional importance since the B5 molecule is known to be involved in an activation pathway of T cells but not of thymocytes or B cells.

Animals↗
PubMed1989

Restricted expression of CD2 among subsets of sheep thymocytes and T lymphocytes.

A monoclonal antibody (mAb) generated against sheep T-cell blasts, called I/35 A, blocks sheep autologous E rosetting and competes with purified T11 target structure (TS), the sheep form of LFA3, for binding sites on the sheep T-cell surface. Immunoprecipitation from lysates of surface iodinated sheep T cells identifies the cell surface molecule recognized by mAb I/35 A as a single chain polypeptide migrating as a diffuse band of MW 55,000. From its binding properties and the biochemical nature of the target antigen, we conclude that mAb I/35 A is directed at sheep CD2. This finding makes sheep the first animal model in which the CD2-LFA3 (T11TS) system is defined by mAbs to both receptor and ligand. When analysed by two-colour flow cytometry and by immunohistochemistry, the cellular expression of CD2 in sheep differs significantly to that reported in humans. In peripheral blood, CD2 is found exclusively on CD4+8- and CD4-8+ T cells, while the third, CD4-8- (predominantly SBU-T19+) subset of sheep T cells (around 20% in peripheral blood) is CD2-. In thymus, only low to moderate levels of CD2 expression occurs on 80% of cells. Among these, medullary 'single positive' thymocytes express the highest level of CD2, whereas the CD4-8- 'double negative' population (which in contrast to peripheral CD4-8- T cells contains only very few SBU-T19+ cells) consists of CD2- and weakly positive cells. In peripheral lymphoid organs, CD2+ lymphocytes occur in the T-cell regions of spleen, lymph nodes and jejunal Peyer's patches (JPP). Tissue macrophages found in B-cell follicles of lymph nodes and JPP are also CD2+. The implications of these findings are discussed in terms of the role CD2 plays in the proliferation of immature thymocytes and of the possible importance of CD2/LFA3 interactions in lymphocyte recirculation.

Animals↗
PubMed1989

Surface expression of differentiation antigens on lymphocytes in the ileal and jejunal Peyer's patches of lambs.

The surface phenotype of lymphocytes in the ileal (IPP) and jejunal (JPP) Peyer's patches (PP) of lambs was compared using flow cytometry and immunohistology with a panel of monoclonal antibodies (mAb). The B-cell markers p220, BAS9A and surface Ig molecules were detected on 70-95% of cells from the IPP. T-cell markers were detected on less than 1% of IPP lymphocytes, confirming that the IPP in lambs contains virtually only B lymphocytes. The JPP contained a lower proportion of B cells and 16% T cells, nearly all of which expressed the CD4 molecule. Interestingly, the reactivity of a fourth B-cell markers, BAQ44a, differed from this pattern; only 12% of IPP lymphocytes were positive whereas 70% of JPP lymphocytes expressed this marker. A majority of both IPP and JPP lymphocytes (80-95%) expressed the cell adhesion molecules CD11a (LFA-1) and LFA-3. Other adhesion molecules, such as CD2 and CD44, were expressed by fewer cells from the IPP than from the JPP. MHC class I antigens were detected on more than 95% of lymphocytes from both the IPP and JPP. In the case of MHC class II antigens, more positive cells occurred in the IPP (greater than 95%) than in the JPP (80%). The in situ localization of cell-surface antigens was assessed by immunohistology. CD4+ T cells occurred in the interfollicular T-cell regions and in JPP follicles, whereas CD8+ T cells localized only in the interfollicular regions and were absent from follicles. The pattern of expression of B-cell markers, adhesion molecules and MHC antigens indicated that a gradient of increasing maturity of B cells existed within follicles from the base towards the dome region. The data presented here lend support to the notion that the IPP in lambs represents a novel B-cell lymphoid tissue with a function different from that of the conventional Peyer's patches found in the jejunum.

Animals↗
PubMed1988

A novel glycoprotein expressed on sheep T and B lymphocytes is involved in a T cell activation pathway.

We have produced a new mouse mAb that identifies a sheep T cell activation Ag. The mAb B5-5 is specific for low m.w. components on nearly all sheep thymocytes and peripheral T and B lymphocytes but does not label immature B cells in Peyer's patches or germinal centers. After cross-linking of target structures either directly by plastic-bound mAb or indirectly using anti-Ig reagents, peripheral T cells, but not thymocytes or peripheral B cells, were activated. IL-2 was secreted by T cells after cross-linking and activation was strongly augmented in the presence of PMA. The addition of soluble B5-5 mAb to mitogen-stimulated cultures of sheep lymphocytes resulted in a suppression of PHA responses and augmentation of PWM responses and had a variable effect on Con A responses but had no effect on LPS- or protein A-induced proliferation. When added to alloantigen-stimulated cultures, B5-5 augmented the proliferative response. The B5-5 membrane component consists of 14- to 19-kDa glycoproteins but the banding patterns obtained during SDS-PAGE analysis of 125I-labeled Ag differed between thymocytes, peripheral T cells, and peripheral B cells. On the basis of its range of expression on lymphoid cells and known biochemical and functional properties, we conclude that the B5-5 component on sheep lymphocytes is different from T cell activation Ag in other species.

Animals↗
PubMed1988

Unusual expression of CD2 in sheep: implications for T cell interactions.

The CD2 adhesion/activation molecule on the surface of mammalian T lymphocytes binds to a ubiquitous receptor, LFA-3. We show that CD2 in sheep differs significantly in its expression from CD2 in humans, and this most likely relates to the high level of expression of the sheep LFA-3 molecule. In sheep, in contrast to man, CD2 was weakly expressed on peripheral T cells and thymocytes. Moreover, a large subset of T cells identified by the monoclonal antibody T19 and considered to be gamma/delta receptor-bearing T cells completely lacked the CD2 molecule. T19+ cells constituted up to 50% of peripheral blood T cells in lambs, and 20-30% of T cells in older sheep, whereas the CD4+ and CD8+ subsets, which are both CD2+, constituted relatively small subsets in peripheral blood. Only those T cells which did express CD2 adhered as "rosettes" to dendritic cells, and the localization of CD2 to the membrane junction indicated that CD2 was critical for this adhesion. However, CD2 adhesion was not necessary for CTL-mediated killing of allogeneic target cells, since T19+ cells generated in bulk mixed lymphocyte culture were extremely efficient at killing appropriate target cells. Some of the behavioral differences between T19+ and CD4+/CD8+ subsets might be explained by the presence or absence of CD2. The results also indicate that the expression of CD2 (and LFA-3) may differ markedly between species.

Animals↗