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1 d block LTB(4)-regulated adhesion molecules (beta2 integrins).
2 not abolished by the TTT/AAA mutation in the beta2 integrin.
3 ndent upon intracellular calcium, and on the beta2 integrin.
4 alphavbeta3 integrin, and leukocyte CD44 and beta2 integrin.
5 ein regulating PMN trafficking downstream of beta2 integrins.
6 ndent post-translational regulation of beta1/beta2 integrins.
7 ating on surfaces that cross-linked cellular beta2 integrins.
8 g through selectins to firm adhesion through beta2 integrins.
9 ating neutrophils displayed normal levels of beta2 integrins.
10 fting usage away from beta1 integrins toward beta2 integrins.
11 of beta1 and beta3 subfamilies, but not with beta2 integrins.
12 despite the normal display of high-affinity beta2 integrins.
13 ectin and expression of membrane-bound beta1/beta2-integrins.
14 operation between selectins, G-proteins, and beta2-integrins.
15 pression of ICAM-1, the ligand for leukocyte beta2-integrins.
16 CXCR2 functions, including the activation of beta2-integrins.
19 smic domain, thereby being indispensable for beta2 integrin activation and neutrophil recruitment.
22 lls exhibited a striking defect in beta1 and beta2 integrin activation in response to Mn(2+) or Mg(2+
23 unteracted selectin- and chemokine-triggered beta2 integrin activation on PMNs by activating protein
24 seven mAb epitopes that are associated with beta2 integrin activation, suggesting that it exhibited
26 its in patients with pDGS by disrupting both beta2-integrin activation and activating receptor accumu
27 a novel Rap1 effector, regulates beta1- and beta2-integrin activation and controls neutrophil chemot
28 inhibitory effect of GDF-15 on CXCL1-induced beta2-integrin activation and neutrophil diapedesis.
30 nitial pathogen recognition by TLRs to rapid beta2-integrin activation may critically regulate acute
34 ulatory input of PI3K into the regulation of beta2 integrin activity, and processes dependent on this
36 lood) and mouse lung ILC2s express beta1 and beta2 integrin adhesion molecules and whether these inte
37 assessed for surface expression of beta1 and beta2 integrin adhesion molecules by using flow cytometr
38 ion explored the mechanism for inhibition of beta2 integrin adhesion molecules when neutrophils are e
39 noclonal antibody to the CD18 subunit of the beta2 integrin adhesion receptors (rhuMAb CD18), in redu
41 hils, we show that FlnA negatively regulates beta2 integrin adhesion to complement component iC3b and
42 DAP expression yet show defects in beta1 and beta2 integrin adhesion, leukocyte function-associated a
43 between ITGAM and SLE implicates the alpha(M)beta2-integrin adhesion pathway in disease development.
44 5b rescues the expression of activated beta1/beta2-integrins, adhesion and bone marrow homing of Klf5
45 ars that P. gingivalis proactively modulates beta2 integrin adhesive activity for intracellular uptak
50 In cis interactions between Jurkat T-cell beta2 integrins and CD47 were detected by fluorescence l
51 tion of type I IFN signaling by ITAM-coupled beta2 integrins and demonstrate that ITAM signaling qual
52 w that high-avidity ligation of ITAM-coupled beta2 integrins and FcgammaRs in macrophages inhibited t
54 s suggest that the relative contributions of beta2 integrins and ICAM-3 to neutrophil adhesion is reg
55 esults demonstrate that CD47 associates with beta2 integrins and is necessary to induce high-affinity
56 moattractant-induced activation of beta1 and beta2 integrins and of chemotaxis is defective in mononu
59 ukocyte (PMN) adhesion via downregulation of beta2-integrins and decreases the efficiency of PMN in t
60 we show that loss of the interaction between beta2-integrins and kindlin-3 abolishes the actin-linkag
62 Thus, Skap2 is essential to activate the beta2 integrins, and loss of Skap2 function is sufficien
63 ls were attenuated by blocking antibodies to beta2 integrins, and the caspase-3 cleavage was attenuat
67 Confocal microscopic analysis revealed that beta2 integrins are present on monocytes after initial a
68 CD177 ligation enhanced its interaction with beta2 integrins, as revealed by fluorescence lifetime im
69 n of vimentin, alpha-smooth muscle actin and beta2-integrin, as well as the production of abundant ex
70 egulation of alphav/beta3, alphav/beta5, and beta2 integrins, associated with increased cortactin exp
72 adhesion deficiency-1 (LAD-I) do not express beta2 integrins because of mutations in the gene specify
73 t that the cooperativity of alpha4beta1 with beta2 integrins becomes evident when they are concurrent
75 sing IL-8 production and interrupting ICAM-1-beta2 integrin binding of melanoma cells to the endothel
77 cted for adhesive function, we find that the beta2 integrin bonds activated in Mn2+ or Mg2+ possess s
78 4- or fMLP-stimulated expression of beta1 or beta2 integrins, but did exert a small inhibitory effect
79 products induce the functional activation of beta2 integrins, but the signaling events that link memb
80 de, we identified colocalization of Ly6G and beta2-integrins by confocal microscopy and confirmed clo
81 Mutation of the kindlin-3 binding site in beta2 integrins caused a loss of firm adhesion of T cell
88 ling from Toll-like receptor 2 (TLR2) to the beta2 integrin CD11b/CD18, leading to the induction of t
90 on of CD11b, the alpha subunit of the alphaM/beta2 integrin (CD11b/CD18), macrophage-1 antigen, or co
92 stitutively and physically associated with a beta2 integrin, CD11b, and cross-linking of CD66b induce
94 population that constitutively expresses the beta2 integrin CD11c and displays a biased central memor
96 is characterized by absent or dysfunctional beta2 integrin (CD18), leading to defective chemotaxis,
97 eficient in the alphaE integrin (CD103), the beta2 integrin (CD18), or the recombination activating g
101 immunodeficiency caused by mutations in the beta2 integrin, CD18, that impair CD11/CD18 heterodimer
102 mice expressing reduced levels of the common beta2 integrin chain develop aggravated Lyme carditis, c
107 s in response to C. albicans mediated by the beta2 integrin, complement receptor 3 (CR3, CD11b/CD18,
108 monocytes, resulting in monocytic beta1- and beta2-integrin conformational change toward an extended,
111 he data provide a novel example of beta1 and beta2 integrin crosstalk in stem/progenitor cell mobiliz
112 feron-gamma-inducible protein-10, beta1- and beta2-integrins, cyclooxygenase-2 (COX-2), monocyte chem
113 and binding of talin-1 and kindlin-3 to the beta2 integrin cytoplasmic domain, thereby being indispe
116 the leukocyte recruitment defect observed in beta2 integrin-deficient (CD18(-/-)) mice, Hck(-/-)Fgr(-
118 ll-cell contact-dependent signaling involved beta2 integrins, dendritic cell-specific ICAM-3-grabbing
119 and c-Jun N-terminal kinase 1 that was also beta2-integrin dependent; pharmacologic inhibition of th
122 asts from the subject demonstrated deficient beta2 integrin-dependent adhesive function similar to th
123 ular stores to the venular surface triggered beta2 integrin-dependent arrest of neutrophils rolling o
125 that Vav proteins are required for multiple beta2 integrin-dependent functions, including sustained
129 regulation of beta2 integrin-independent and beta2 integrin-dependent migration, respectively, reveal
133 ough a novel pathway involving regulation of beta2-integrin-dependent adhesion, NADPH oxidase, and a
136 shown to function as a negative regulator of beta2-integrin-dependent neutrophil recruitment to the l
138 le blocking mAb to the alpha subunits of the beta2 integrins each partially blocked the O2- response.
139 h face cumulative stimulations by TNF-alpha, beta2-integrin engagement, C5a, and ANCA by the FcgammaR
140 okine receptor (CCR2) and adhesion receptor (beta2 integrin) engagement leads to an interaction betwe
143 adoptive transfer and early accumulation of beta2 integrin-expressing CD4+ T cells in the gastrointe
144 D177-driven cell activation enhanced surface beta2 integrin expression and affinity, impaired interna
145 s demonstrate that hypoxia induces leukocyte beta2 integrin expression and function by transcriptiona
146 psoriasiform dermatitis due to reduced CD18/beta2 integrin expression to 2-16% of wild-type levels,
148 nal upregulation of integrin signaling, with beta2-integrin expression being modulated by NOTCH1 muta
149 f5(Delta/Delta) mice, and reduced beta1- and beta2-integrin expression on hematopoietic progenitors s
151 These genes encode the alpha subunits of the beta2 integrin family of leukocyte adhesion receptors.
153 naling involves specific phosphorylations of beta2 integrin followed by interactions with cytoplasmic
154 tion: a first signal that also activates PMN beta2 integrins, followed by a second, beta2 integrin-me
156 very low doses of cytochalasin D disconnect beta2-integrins from their cytoskeletal links, allowing
160 against the possibility that CD37 regulates beta2 integrin function via a direct molecular interacti
161 a second exposure is required for increased beta2 integrin function, intravascular neutrophil aggreg
163 plate flow chamber to define the dynamics of beta2-integrin function during recruitment and transmigr
164 Our data suggest that strategies to target beta2 integrin have clinical potential to alleviate or p
167 lular adhesion, in particular the CD11b/CD18 beta2 integrin heterodimer complement receptor type 3/Ma
169 ack of CD18 results in the deficiency of all beta2 integrins, i.e., CD11a/CD18 (LFA-1), CD11b/CD18 (M
178 acquisition of cooperation between beta1 and beta2 integrins in the cell/substrate adhesive interacti
180 Anti-Ly6G Ab impaired surface expression of beta2-integrins in LTB(4)-stimulated neutrophils and mim
181 rdance with these findings, we observed that beta2 integrins, including Mac-1, trigger proliferation
182 comitant negative and positive regulation of beta2 integrin-independent and beta2 integrin-dependent
183 ed a profound defect in adhesion mediated by beta2 integrins indicative of a variant form of LAD-1.
185 ulation of beta1-integrin, overexpression of beta2-integrin, inhibited phosphorylation of focal adhes
186 effectively rescued by treatment with either beta2-integrin inhibitory antibodies or FAK inhibitors.
189 However, the specific roles of kindlin-3-beta2-integrin interactions in T-cell adhesion and homin
190 prevented by depleting neutrophils, blocking beta2 integrin-intercellular adhesion molecule 1 interac
193 eptide of ruminant CD18, the beta subunit of beta2 integrins, is not cleaved and hence remains intact
194 pted in mice lacking adhesion molecules like beta2-integrins (Itgb2-/-) which have defective neutroph
195 w that basal Ab levels are normal in TTT/AAA beta2-integrin KI mice, but B cell numbers in lymph node
198 esulted in profound defects in clustering of beta2 integrins, leading to defective adhesion and trans
199 RP1 also is implicated because inhibition of beta2-integrins led to increased VWF levels in control (
200 of intercellular adhesion molecule-1 to the beta2-integrin leukocyte function associated antigen-1 (
204 ll receptors, we show that engagement of the beta2 integrin LFA-1 on NK cells by intercellular adhesi
205 o target cells was not attributed to altered beta2 integrin LFA-1 properties but was instead due to r
209 dhesion of CD37-deficient neutrophils to the beta2 integrin ligand, ICAM-1, despite the normal displa
211 eactive oxygen species (ROS) following CD11b beta2-integrin ligation with fibrinogen in a sialic acid
212 ntegrin-responsive actin assembly and alphaM/beta2 integrin localization are compromised in Arpc2(-/-
213 y molecule CD154, the CD4 coreceptor, or the beta2 integrin lymphocyte function-associated antigen (L
214 uring inflammation critically depends on the beta2 integrins lymphocyte function-associated antigen 1
215 treated with C1q were found to activate the beta2 integrins lymphocyte function-associated antigen 1
217 sels before an adhesion step mediated by the beta2 integrins, lymphocyte function-associated antigen
219 heterophilic interaction with the leukocyte beta2 integrin Mac-1, thereby mediating interactions bet
220 - in particular, increased expression of the beta2-integrin Mac-1 (alphaMbeta2, or CD11b/CD18), which
221 n to be a counter receptor for the leukocyte beta2-integrin Mac-1 (CD11b/CD18), thereby mediating int
222 tment was prevented in mice deficient in the beta2-integrin Mac-1 but not in those deficient in LFA-1
223 , via its apo(a) moiety, is a ligand for the beta2-integrin Mac-1, thereby facilitating inflammatory
224 moiety Lp(a) specifically interacts with the beta2-integrin Mac-1, thereby promoting the adhesion of
225 reted ACT binds to macrophages utilizing the beta2 integrin, Mac-1 (CR3, CD11b/CD18), and subsequent
226 optosis that is inhibited by antibody to the beta2 integrin, Mac-1, and requires NADPH oxidase-derive
230 In response to SS RBCs, leukocyte CD44 and beta2 integrins mediated PBMC adhesion to ECs, a process
231 ulation with TNFalpha was found to result in beta2 integrin-mediated activation of the cytoplasmic ty
233 ils had markedly impaired chemokine-induced, beta2 integrin-mediated arrest, spreading, and migration
234 a surrogate vessel wall and can also support beta2 integrin-mediated immobilization of neutrophils if
237 s PMN beta2 integrins, followed by a second, beta2 integrin-mediated signal, which occurs physiologic
238 utrophils exhibited normal selectin-induced, beta2 integrin-mediated slow rolling, in sharp contrast
241 ed to the membrane of neutrophils engaged in beta2-integrin-mediated adhesion, while these antigens a
242 grins on hematopoietic cells, especially the beta2 integrins, mice and primates were treated with ant
246 ils that trigger activation of high-affinity beta2-integrins necessary for transition to shear-resist
248 alphaLbeta2 immobilized on microspheres and beta2 integrin on neutrophils, we quantified an impressi
249 alphaLbeta2 immobilized on microspheres and beta2 integrin on neutrophils, we quantified an impressi
252 osinophil adhesion to HCEs in vitro involved beta2 integrins on eosinophils but not intercellular adh
253 uidic device, that a substantial fraction of beta2 integrins on human neutrophils acquire an unexpect
254 is critical in hemostasis, and the beta1 and beta2 integrins on leukocytes have many roles in cell-me
255 ion molecule-1 (ICAM-1) on melanoma cells to beta2 integrins on PMNs, which is mediated by endogenous
256 sent study we examine bond formation between beta2-integrins on neutrophils and immobilized ICAM-1 wh
257 Simultaneous engagement of ITAM-coupled beta2 integrins or Dectin-1 with TLR4 did not affect TLR
258 metalloproteinase 9 (MMP-9), G-CSF receptor, beta2 integrins, or selectins responded to Ptx treatment
261 onsequently, attenuation of IFN responses by beta2 integrins protected primary human macrophages from
263 neutrophils from beta2 null mice identified beta2 integrin receptors as a master switch for NET indu
265 based on experiments performed with chimeric beta2-integrins recombinantly expressed in a cell line t
266 n of Rab5 family members, mediators of beta1/beta2-integrin recycling in the early endosome, is decre
267 y to the alpha-subunit of Mac-1, a leukocyte beta2 integrin required for innate immunity to invading
268 firm adhesion are known to be selectins and beta2 -integrins, respectively, the precise dynamic mech
270 itor, piceatannol, which blocks 'outside-in' beta2 integrin signalling in leukocytes, detached the ad
274 stablish a structure and function map of the beta2 integrin subunit, we mapped the epitopes of a pane
275 Pretreatment of monocytes with mAb to the beta2-integrin subunit CD18 decreased adhesion and aboli
278 pathways to induce conformational changes in beta2 integrins that allow these phagocytes to effective
279 signaling, by means including activation of beta2 integrins that are coupled to the ITAM-containing
280 coronin 1A (Coro1A) as a novel regulator of beta2 integrins that interacts with the cytoplasmic tail
282 promoting the high affinity conformation of beta2 integrins, thereby facilitating PMN trafficking du
283 irect assay for the off-rates of ICAM-1 from beta2 integrin throughout the course of each experiment.
284 del of psoriasis, reduced expression of CD18/beta2 integrin to 2-16% of wild-type levels is associate
289 ction circuit that rapidly converts extended beta2-integrins to high-affinity shear-resistant bond cl
290 eficient, neutrophils into mice deficient in beta2 integrins transiently decreases neutrophilia and r
291 to induce strong activation of the beta1 and beta2 integrins via an avidity-modulation mechanism.
292 dency of these inflammatory processes on the beta2 integrins was investigated in CD18 hypomorph mice,
294 dependent on chemokines but not on beta1 or beta2 integrins, was observed in loose fibronectin and c
295 To determine the function of individual beta2 integrins, we examined CD8 T cell responses to Lis
296 n addition, the adhesion molecules beta1 and beta2 integrins were found to be crucial for EAR secreti
297 hat initial monocyte adhesion is mediated by beta2 integrins, whereas during the induction of macroph
299 tin in vitro and in vivo, failed to activate beta2 integrins while rolling, and did not emigrate into
300 ng segment 1 fibronectin and interactions of beta2 integrins with endothelial intercellular adhesion
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