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Inducibility and Expression of Microvascular Endothelial Adhesion Molecules in Lesional, Perilesional, and Uninvolved Skin of Psoriatic Patients Peter Petzelbauer, Jordan S. Pober, Agnes Keh,* and Irwin M. Braverman* Boyer Center for Molecular Medicine and - D epartment of D ermatolo gy, Yale University School of M edicine, New Haven, Connecticut, U.S.A. Previous studies have demonstrated 1) that patterns of inducible endothelial cell expression of endothelial leukocyte adhesion molecule-l (ELAM-l) and vascular cell adhesion molecule-l (VCAM-l) in response to cytokines varies both with anatomic position within the dermal microvasculature and with the presence of perivascular inflammatory infiltrates, and 2) that the anatomic architecture of the dermal superficial plexus (SVP) is altered in inflamed lesional but not in univolved skin of psoriatic patients. The present study was designed to evaluate the pattern of cytokine inducibility ofELAM-l and VCAM-l in altered dermal microvessels of psoriatic patients. At the light microscope level, preculture biopsies of uninvolved and perilesional skin were indistinguishable by morphology and ELAM-l and VCAM-l expression were virtually absent. In contrast, biopsied lesional skin showed elongated capillary loops and increased numbers ofT cells compared to uninvolved and perilesional skin. The dermal microvasculature of the SVP of lesional skin contained ELAM-l+ in 29.4% of vessels and VCAM-l+ endothelial cells in 8.7% of vessels. After 24 h of organ culture in medium supplemented with tumor necrosis factor and interleukin-4, ELAM-l + endothelial cells in the SVP were increased significantly in uninvolved (from mean 0.5% to 27% of vessels), perilesional (from mean 5.5% to 41.8% of vessels), and lesional skin (from mean 29.4% to 45.7% of vessels) . VCAM-l was not inducible on SVP endothelial cells in uninvolved skin but VCAM- l+ endothelial cells were increased significantly in perilesional (from mean 0.7% to 23.7% of vessels) and lesional skin (from mean 8.7% to 41.4% of vessels). In uninvolved and perilesional skin ELAM-l and VCAM-l were confined to endothelial cells below the rete. In contrast, endothelial cells of the intrapapillary part of the capillary loop oflesional skin became cytokine responsive, in that ELAM-l and VCAM-l could be induced at this site. By immunoelectron microscopy, expression was most intense on the luminal surface of venular endothelial cells and at the inter endothelial junctions. In conclusion, we have presented evidence that the cytokine responsiveness of microvascular endothelial cells is altered in psoriasis in a pattern that may explain both the circumscribed nature and the epidermal involvement of the psoriatic plaque. Key words: ELAM-1 / VCAM-1 / organ culture/ superficial vascular plexus.] Invest DermatoI103:300-305, 1994 icrovascular endothelial cells of human skin contribute to the recruitment of inflammatory leukocytes by expressing inducible leukocyte adhesion molecules such as endothelial leukocyte adhesion molecule-1 (ELAM-l, also called E-selectin) , vascular cell adhesion molecule-1 (VCAM-1), and intercell ular adhesion molecule-l (ICAM-1 , also called CD54). ELAM- l appears particularly important in the recruitment of neutrophils and may also participate in recruitment of other leukocytes such as inflammatory T cell s and monocytes [1,2]. VCAM-l contributes to selective recruitment of T cells and eosinophils but not neutrophils [1 ,3,4]. Elevated IC AM-1 also appears more closely associated with T-cell infiltration ill lIillo [5,6]' but also contributes to neutrophil adhesion and transmigration in vitro [1,7]. I " vivo as well as cell and organ-culture experiments have identified inflammatory cytokines, including interleukin (IL)-l, tumor necrosis factor (TNF), interferon (IFN)-y, and IL-4, as the major signals that induce the expression of these adhesion mo lecules [8 - 15]. Furthermore, skin organculture experiments have revealed that the responsiveness of microvascular endothelial cells to cytokines varies with anatomic position. Specifically, in the superficial vascular plexus (SVP), inducible ELAM-1 expression is largely confined to the venules of the horizontal plexus and the venular portions of the capillary loops, i.e. , that portion below the level of the rete just proximal to anastomosis with the horizontal vessels [15]. TNF and IL-l are the most potent signals for induction ofELAM-l. VCAM-l , in normal skin, is not inducible on endothelial cells of the SVP by any combination of cytokines and its expression is confined largely to vessels of the deep vascular plexus. In organ-cultured acutely inflamed skin, ELAM-l is basally expressed and VCAM-l becomes inducible on SVP venular endothelial cells by a combination of TNF and IL-4. Even in dermatitis, these adhesion molecules M Manuscript received N ovember 10 , 1993; accepted for publication March 28, 1994. Reprint requests to: Dr. Peter Petze lbauer, Department of Dermatology, University o[V ienna, A-I090 Vienna, Austria. Abbreviations: SVP, superficia l vascular plexus; UEA I, ulex ellropeus agglutinin I. 0022-202X!94!S07.00 Copyright © 1994 by The Society for Investigative D ermatology,Inc. 300 VOL. 103, NO.3 SEPTEMBER 1994 cannot be induced on the intrapapillary parts of the capillary loops [1 ?fhe architecture of the SVP is altered in psoriasis. Specifically, the capillary loops of lesional skin are tortuous and elongated [16] and the normally well-defined boundary between capillary endothelial cells resting on an arteriolar-like homogeneous basement membrane and endothelial cells on a venular-like laminated basement membrane are aberrant [17]. Microvascular endothelial cells in lesional psoriatic skin express both ELAM-1 and VCAM-1 molecules [10,18], but the anatomic distributions and cytokine responsiveness of altered psoriatic microvessels have not previously been described. In addition, the evaluation of perilesional microvessels presents the opportu~ity ~o sepa~at~ the contributio~s of primary microvascular alteratlOllS 111 psonasls from those of 1I1flammation observed in lesional vessels. C YTOKlNE RESPONSIVENESS OF PSORIATIC ENDOTHELIUM 60 ELAM · ' uninvolve d skin 60 VC AM· , uninvol ve d skin T cells I HPF --<>-- 60 ELAM · ' pe rilesional skin 60 VC AM · ' perilesional skin T col!s / HPF --- --<>-- skin Specimens Trunk skin of eight different psoriatic patients, ranging --0-- in age from 40 to 60 years, was obtained according to a protocol approved by the Yale Human Investigations Committee. Superficial 3-mm punch biopsies were taken from lesional skin (n = 7; six with plaque-type and one with guttate psoriasis), from normal~appearing skin at a 5- to 10-mm distance from the leSion (penleslOnal skill, n = 8), and from chlllcally umnvolved skin at sites at least 50 mm away from the nearest lesion (uninvolved skin, Skin Organ Culture Each punch biopsy was bisected perpendicular to the epidermis. One part was immediately embedded in OCT (Miles, Naperville, IL), snap frozen, and stored at -70 ' C. The other half was placed in skin organ cultures as described previously [15]. In brief, skin specimens were placed in C24-well plates (Falcon, Bedford, MA) with the epidermis facing up, and attached to the plastic by air drying. RPMI 1640 culture medium (Gibco, Grand Island, NY) supplemented with 10% human AB serum (vol/vol; Gibco), L-glutamine (10 mM; Gibco), penicillin (100 U/ rnl; Gibco), streptomycin (100 ,ug/ml; Gibco), recombinant TNF, 200 U/ mI, obtained from Biogen (Cambridge, MA), and recombinant IL-4, 2000 V/ml, obtained from Schering Plough Research (Bloomfield, NJ) was gently added to each well so that just the epidermis remained uncovered. This combination and dosage of cytokines was identified previously as that producing maximal changes in VCAM-l expression on dermal microvascular endothelial cells (DMECs) in organ culture [15]. Explants were incubated at 37" C in humidified CO 2 /95% air for 24 h. At the end of the incubation period, explants were embedded in OCT and snap frozen. Monoclonal Antibodies (MoAbs) and Lectins The following mouse MoAbs wereIgG1 isotypes: anti - ELAM-1 (H4/18), anti- VCAM- 1 (E1/6; gift of M .P. Bevilacqua, Universiry of California at San Diego, San Diego, CAl, anti-CD36 {OKM-5; Ortho, Raritan, NJ, and non-binding control (K16/16; gift of D.L. Mendrick, Brigham and Women's Hospital, Boston, MA) . Mouse anti-human CD3, COla, and CD68 MoAbs were IgG2a isotypes and obtained from Dakopatts (Carpinteria, CAl. Ulex europells agglutinin I {UEA I)-biotin was purchased from Vector Labs (Burlingame, CAl. Inununohistochemistry Four-micrometer sections were processed and double-stained as described [15]. In brief, the first MoAb {H4/18, El/6, or OKM-5} was visualized using the alkaline phosphatase anti-alkaline phosphatase (APAAP) technique and stained in blue by the alkaline phospatase substrate kit obtained from Vector. The biotinylatcd lectin UEA I was visualized using peroxidase-labeled avidin-biotin complexes and stained in red by 3-amino-9-ethylcarbazole (Sigma Chemical Co., St. Louis, MO). Controls were performed by using a non-binding control MoAb (K16/16) as a first-step reagent and/or by omitting the lectin. For CDla, CD3, or CD68 antigens, single antibody staining was performed using the peroxidase VectaStain ABC kit (Vector). Scoring and Statistical Analysis CD36, ELAM-l and VCAM-l expression on endothelial cells were quantified on sections double stained with UEA I as described [15] . The total number of vascular profiles (as identified by UEA I staining) within the superficial vascular plexus (SVP) was determined in four randomly selected high-power fields in two different sections/skin specimens and then the number of CD36-, ELAM-1 - , and VCAM-l-positive vessels were determined in the same fields. Vessels of the deep vascular plexus were excluded because the deeper portions of the dermis were usually not present in the biopsy specimens. Vessel cross-sections were considered to be positively stained when at least one cell in the cross-section was clearly reactive with the specific MoAb. Staining intensity was not considered. Data are expressed as the percentage of the total vessels 7 8 5 7 MATERIALS AND METHODS n =4). 301 60 ELAM· ' lesionai skin 60 6 8 6 9 4 9 57 16 VCAM· ' lesio nal skin T cells I H PF ---0--- ---- ptO- cu ltured s k in pre cu l1 ured sk in CYloktnoInduced phenotype 46 200 120 --0-- - 26 26 ------- "0 45 c yloki noInduced phenolype Figure 1. Percentage of ELAM-l+ or VCAM-l+ SVP vessel crosssections in uninvolved, perilesional, and lesional psoriatic skin. Each liue connects preculture valu.es (left). with the percentage of positive vessels after 24 h of organ culture 111 medium supplemented with TNF and IL-4 (right) of an individual skin specimen evaluated as described in Materials OIl d Methods. The numbers to the right of the figure indicate the densities of CI?3+ cells within the papillary dermis for uninvolved , perivascular, or leslOual skill pnor to culture. Although VCAM-l expression is significantly II1duclble III organ-cultured penleslOnal skin, the density of dermal T cells in perilesional skin is comparable to th at seen in uninvolved skin. (UEA 1+) in the SVP showing C D36 , ELAM-I, or VCAM-l expression . Num~ers of T+ cells were quantified in the preculture skin specimen by countlllg CD3 cells I~ four lugh-power fields (HPF; 0.5 mm in diameter) wlthlll the upper dernus Il1 two different sections and the mean densiry / HPF was detenlll~l~d. All specllnens were scored by a single observer (PP) blinded to th e conditIOns .. The interobserver correlation coefficient (R2) has been preVIOusly determllled as being 0.95 [15]. Data were pooled for each rype of specimen {lesional, perilesional , or normal skin} and for each MoAb, and are presented as mean ± SEM. Statistics were performed using the Student t test. Immunoelectron Microscopy The organ-culture specimens were hand cut into approximately 100-lim sections and fixed by immersion in 30/0 paraformaldehyde in 0.1 M phosphate buffer, pH 7.4, for 2 h at 4' C , followed by rinsing in phosphate buffer for 1 h. Immunohistochemistry was performed using the peroxidase Vectastain ABC kit (Vector) . The sections were incubated with the prima.ry MoAbs (H4/ 18 and E1 / 6) overnight at 4 ' C and the reaction products were visualized with diaminobezidine (Sigma). Sections were post-fixed with half-strength Karnovsky 's fixative and .wlth 1% OS04 and then embedded in Spurr's epoxy res in [19). Ultrathin sectIOns were prepared for viewin g usin g a Zeiss electron microscope model EM-l09. RESULTS Uninvolved Skin The mean density of CD3+ cells/HPF in uninvolved skin from psoriatic patients was 6.7 ± 0.6 (Fig 1), which 302 PETZELBAUER ET AL is comparable to previously published CD3 counts in normal skin [20]. In the preculture specimens, endothelial cells did not express ELAM-l (0.5% ± 0.5% of vessels) or VCAM-l (0.7% ± 0.7% of vessels) molecules, consistent with previous reports [15,21]. The percentage of CD36+ vessel cross-sections within the SVP ranged from 15% to 25%, which is identical to that seen in normal nonpsoriatic skin specimens [15]. CD36 molecule expression was unaltered by the cytokine treatment used and no differences were observed among uninvolved, periesional, or lesional skin specimens and will not be discussed further. When uninvolved skin was placed in organ-culture medium supplemented with TNF and IL-4 for 24 h, ELAM-l expression on endothelial cells was significantly upregulated (27% ± 1.7% of vessels; p < 0.001 compared to precultured skin; Fig 1) and was restricted to venular endothelial cells. This extent of ELAM-l upregulation is comparable to that seen in normal, non-psoriatic skin [15]. The capillary loops within the tips of the papillae above the lower level of the rete ridges remained ELAM-l negative, as previously noted in normal skin [15] . VCAM-l expression on endothelial cells was undetectable after 24 h of organ culture (1.5% ± 1.0% of vessels; Figs 1,2a), also consistent with previous findings in endothelial cells of the SVP in normal skin. Perilesional Skin At the light microscope level, perilesional skin was generally indistinguishable from uninvolved skin in terms of vascularization and density of dermal leukocytes. The rete were not elongated in any of the eight specimens, although the epidermis in two of eight specimens was slightly acanthotic. The mean density of CD3+ cells/HPF was 14.3 ± 6.2, difference not significant compared to uninvolved skin (Fig 1). The num.bers of CD1a+ dendritic cells and CD68+ macrophages were also comparable to those seen in uninvolved skin (data not shown). Only 5.5% ± 2.3% of vessels contained ELAM-l + endothelial cells, difference not significant compared to uninvolved skin. VCAM-l expression on endothelial cells was virtually undetectable (0.7% ± 0.4% of vessel cross sections ·contained VCAM-l + endothelial cells). After 24 h of organ culture in medium supplemented with TNF and IL-4, ELAM-1 + endothelial cells were significantly increased to 41.8% ± 4.2% of vessel cross-sections (p < 0.001 compared to precultured perilesional skin; Fig 1), which is similar to the findings in uninvolved skin. In striking contrast to uninvolved skin, VCAM-1 expression was induced on endothelial cells in cytokine-treated perilesional skin to a level of 23.7% ± 7.1 % of vessel cross-sections; p < 0.05 compared to precultured skin (Fig 1). The expression of both ELAM-l and VCAM-l (Fig 2b) was restricted to the horizontal venules and the venular limb of the capillary loops below the level of the rete. No ELAM-1+ or VCAM-1+ endothelial cells were noted in the capillary loops above the level of the rete. By immunoelectron microscopy, staining for VCAM-1 molecules was found on the luminal side of the venular endothelial cells and on the interendothelial junctions. VCAM-l + endothelial cells could be detected next to VCAM-1 - endothelial cells within the same microvessel. Lesional Skin Morphologically, lesional specimens showed epidermal hyperproliferation, elongation of the rete ridges, tortuous elongation of the capillary loops, and a moderate perivascular round Figure 2. Uninvolved (a), perilesional (b), and lesional (c) psoriatic skin after 24 h of organ culture in medium supplemented with TNF and IL-4, stained immunohistochemically with anti- VCAM-l MoAb in blue and the panendothelial marker UEA I in red. In uninvolved skin (a), VCAM-l cannot be induced on SVP endothelial cells; in pcrilesional skin (b), VCAM-l expression is found on the horizontal venules of the SVP (arrows). Capillary loops extending upward to the papillae are VCAM-l - (arrowhead). In lesional skin (e), VCAM-l expression is found on capillaries and small venulcs of the SVP (arrows), but also extends upward into the intrapapillary portion of the capillary loop (arrowhead). Bar, SO lim. THE JOURNAL OF INVESTIGATIVE DERMATOLOGY VOL. 1.03, NO.3 SEPTEMBER 1994 C YTOKlNE RESPONSIVENESS OF PSORIATIC ENDOTHELIUM 303 DISCUSSION Figure 3. The proximal part of a dermal capillary loop in lesional psoriatic skin after 24 h of organ culture in medium supplemented with TNF and IL-4 shown in a i-ttm plastic section. The epidermis (E) is separated from the dermal papilla (P); arterial limb (A); venous limb (V). cell infiltrate. The mean density of dermal CD3+ cells/HPF was 81.8 ± 24.4, which is significantly higher than in perilesional or uninvolved skin (p < 0.05; Fig 1). The percentage of vascular pro@es containing ELAM-1+ endothelial cells was 29.4% ± 6% and 8.7% ± 3.2% contained VCAM-1+ endothelial cells (Fig 1). The expression of both molecules was detectable on endothelial cells in the venules of the SVP and in the capillary loops below the lower level of the rete ridges. Of note, these molecules were also expressed on capillary endothelial cells within the tips of the papillae in that part of the loop that is in close anatomical proximity to the basal keratinocytes. In lesional skin, treatment with cytokines in organ culture increased ELAM-1 + endothelial cells to 45.7% ± 3.1 % of vessels; p < 0.05 (Fig 1). VCAM-1+ endothelial cells were further increased to 41.4% ± 4.6% of vascular profiles; p < 0.005 compared to precultured skin (Fig 1), Again, as seen in fresh lesional skin, inducible ELAM-1 and VCAM-1 (Fig 2c) expression was detectable on capillary loops below and above the lower level of the rete ridges. Furthermore, the staining intensity appeared enhanced in organ-cultured skin compared to preculture specimens. Immunoelectron microscopy confirmed the light microscopic observations. Within the horizontal part of the SVP ELAM-1+ and VCAM-1 endothelial cells (Fig 2) were found to be present within venules but not arterioles. Immunoelectron microscopic evaluation was also used to localize ELAM-1 and VCAM-1 within the capillary loops. This is best illustrated by comparing Figs 3 and 4. Figure 3 is a 1-l1m plastic section of organ-cultured lesional skin showing a capillary loop. As seen in Fig 4, only the endothelial cells of the venular side of the loop characterized by a laminated basement membrane express ELAM- l molecules. We have examined the ELAM-1 and VCAM-1 expression patterns in uninvolved, perivascular, and lesional psoriatic skin before and after 24 h of organ culture in medium supplemented with TNF and IL-4. We found that in preculture uninvolved and in perilesional skin ELAM-1 and VCAM-l molecules are virtually absent on SVP endothelium, whereas these molecules are expressed on endothelial cells in lesional skin. After 24 h of cytokine treatment in organ culture. ELAM-l is inducible on venules in uninvolved, perilesional, and in lesional skin. In contrast, VCAM-1 is not inducible in uninvolved skin of psoriatic patients, consistent with our previous report on organ-cultured normal skin of non-psoriatics [15]. Unexpectedly, cytokine stimulation of perilesional skin causes a significant upregulation of VCAM-1 expression on venular endothelial cells of the SVP, compared to the preculture specimen, which is comparable to the cytokine-induced upregulation ofVCAM-1 expression in organ-cultured lesional skin. Arteriolar endothelial cells are consistently ELAM-1 and VCAM-1 negative in all specimens. However, in psoriatic lesional skin, the intrapapillary portion of the capillary loop acquires cytokine responsiveness and is able to express ELAM- 1 or VCAM-1 molecules. These altered cytokille responses parallel the elongation of the venular side of the loop characterized by a laminated basement membrane. The phenotypic change ofSVP endothelial cells consisting in the ability to express VCAM-1 in perilesional psoriatic skin may be relevant to the pathogenesis of psoriasis. VCAM-1 expression has been observed in SVP endothelial cells ill lIillo only in settings of natural or cytokine-induced inflammation [9,18,22,23J, and our previous organ culture experiments of inflamed skin suggested that the infiltrating leukocytes were necessary for endothelial cells to display this capacity [15]. This led us to propose that infiltrating leukocytes provide an as-yet unidentified co-factor that relieved some inhibitory constraint. The present study suggests that SVP endothelial cells can be relieved of this inhibition in the absence of infiltrating leukocytes. The basis of this change is unknown but is consistent with previous observations that the function of the microvasculature in perilesional psoriatic skin is altered. For example, there is increased blood flow in perilesional psoriatic skin in the absence of any microscopically detectable changes [24]. This alteration in the behavior of endothelial cells only at the advancing edge of a psoriatic plaque may contribute to the sharply circumscribed character of psoriatic lesions. The other finding in this paper relevant for the pathogenesis of psoriasis involves the phenotypic alteration of the endothelial cells in the capillary loop in lesional skin of psoriasis that is not found in acute dermatitis [15]. The expression ofELAM-1 and VCAM-1 in this part of the capillary loop that is in proximity to the epidermis probably contributes to the typical histopathologic appearance of psoriatic lesions with epidermotropic neutrophils and T cells. ELAM-1 is important for neutrophil recruitment [1,2]' and thus expression of ELAM-1 at that site could initiate neutrophil traffic into the epidermis that results in the characteristic picture of "mounds of neutrophils on top of parakeratosis," which are typically localized above a tip of a papilla [25]. Epidermotropic T cells that express the ELAM-1 ligand detected with MoAb HECA 452 (sometimes called cutaneous lymphocyte-associated antigen-1) could also adhere in this part of the capillary loop [26,27]. Endothelial cell VCAM-1 interactions with T-cell VLA-4 may aJso contribute to epidermotropism of these cells [2]. These speculations are supported by adhesion assays that demonstrate the enhanced binding of leukocytes, especially CD4+ lymphocytes, to psoriatic SVP endothelium within the intra papillary part of the capillary loop [28-30]. In conclusion, we have presented evidence that the cytokine responsiveness of microvascular endothelial cells is a.ltered in psoriasis in a pattern that may explain both the circumscribed nature and the epidermal involvement of the psoriatic plaque. These findings also suggest the more general proposition that analysis of the contribution of endothelial cell adhesion molecules to inflammatory disease must not only take into account the presence of inflammatory cyto- 304 THE JOURNAL OF INVESTIGATIVE DERMATOLOGY PETZELBAUER ET AL Figure 4. Immunoelectron microscopy ofELAM-l from the section shown in Fig 3. Arterial limb with a homogenous basement membrane (A); venous limb with a laminated basement membrane (V); de granulated mast cells (M). Bar, 111m. Lift upper itlSct, higher magnification of the arterial limb indicated by the box. The endothelial cell (E) surface is nega tive for the peroxidase reaction product. Bar, 111m. Right upper inset, higher magnification of the venous limb indicated by the box and shows the endothelial cell (E) surface positive for the peroxidase reaction product. Bar, 111 m . kines that induce these molecules but the variable ability of specific endothelial cells to respond. 4. 5. 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Br] Dermato!1 27:560 - 565 , 1992 Cotran RS, Gimbrone Jr MA, Bevilacqua MP, Mendrick DL, Pober JS: Induction and detection of human endothelial activation antigen in vivo.] Exp Med 164:661 -666 , 1986 Norris P, Poston RN , Thomas DS , Thornhill M , H awk J, Haskard DO: The expression of endothelial leukocyte adhesion molecule-I (ELAM-1), intercellular adhesion molecule-I (ICAM- I), and vascular cell adhesion molecule-l 28. 29. 30. homing receptor for skin homing T cells.] Illlmu Il0!150:1122-1136, 1993 C hin YH , Fa langa V, Taylor JR, CaiJP, Bax J : Adherence of human heIper/ memory T-cell subsets to psoriatic dermal endothelium.] [ liVest Derlll aloI 94:413 417,1990 Barker IN, Groves R W, Allen MH , MacDonald DM: Preferential ad herence ofT lymphocytes and neutrophils to psoriatic epidermis. Br] Derm ato!127:2052 11 , 1992 Sackstein R, Falanga V, StrcileinJW, C hin YH: Lymphocyte ad hesion to psoriatic dermal endothelium is mediated by a tissue-specific receptor/ ligand interaction.] /tlllest Dermato! 91 :423 - 428 , 1988 ANNOUNCEMENT "The Board of the Austrian Society of Dermatology and Venereology (hoc tempore president, Klaus Wolff, M.D.) has awarded the Ferdinand von Hebra Medal in gold to Professor John Thorne Crissey, University of Southern California, Los Angeles for achievements in the history of medicine (dermatology} ." (Upon application by Karl Holubar, M .D., past president and historian) .