Atherosclerotic Lesions Grow Through Recruitment and Proliferation of Circulating Monocytes in a Murine Model
2002; Elsevier BV; Volume: 160; Issue: 6 Linguagem: Inglês
10.1016/s0002-9440(10)61163-7
ISSN1525-2191
AutoresSusan M. Lessner, Heather L. Prado, Edmund K. Waller, Zorina S. Galis,
Tópico(s)Immune cells in cancer
ResumoMacrophage-derived foam cells in developing atherosclerotic lesions may potentially originate either from recruitment of circulating monocytes or from migration of resident tissue macrophages. In this study, we have determined the source of intimal macrophages in the apoE-knockout mouse flow-cessation/hypercholesterolemia model of atherosclerosis using a bone marrow transplantation approach. We also examined the time course and spatial distribution of intercellular adhesion molecule-1 and vascular cell adhesion molecule-1 expression to assess whether endothelial adhesion molecules were involved in recruitment of either circulating monocytes or resident macrophages. We used allelic variants of the mouse common leukocyte antigen (CD45) to distinguish host-derived and donor-derived white blood cells (WBCs) both in blood and in macrophage-rich carotid lesions. We found that the distribution of CD45 isoforms in lesions is similar to that of circulating WBCs, whereas the host-type CD45 isoform is more prevalent in resident adventitial macrophages. These data indicate that macrophage-derived foam cells in the lesion derive mainly from circulating precursors rather than from resident macrophages. The corresponding time course of intercellular adhesion molecule-1 and vascular cell adhesion molecule-1 expression suggests that recruitment of circulating WBCs by endothelial adhesion molecules is likely to be more important during lesion initiation than during the later phase of rapid lesion growth. Macrophage-derived foam cells in developing atherosclerotic lesions may potentially originate either from recruitment of circulating monocytes or from migration of resident tissue macrophages. In this study, we have determined the source of intimal macrophages in the apoE-knockout mouse flow-cessation/hypercholesterolemia model of atherosclerosis using a bone marrow transplantation approach. We also examined the time course and spatial distribution of intercellular adhesion molecule-1 and vascular cell adhesion molecule-1 expression to assess whether endothelial adhesion molecules were involved in recruitment of either circulating monocytes or resident macrophages. We used allelic variants of the mouse common leukocyte antigen (CD45) to distinguish host-derived and donor-derived white blood cells (WBCs) both in blood and in macrophage-rich carotid lesions. We found that the distribution of CD45 isoforms in lesions is similar to that of circulating WBCs, whereas the host-type CD45 isoform is more prevalent in resident adventitial macrophages. These data indicate that macrophage-derived foam cells in the lesion derive mainly from circulating precursors rather than from resident macrophages. The corresponding time course of intercellular adhesion molecule-1 and vascular cell adhesion molecule-1 expression suggests that recruitment of circulating WBCs by endothelial adhesion molecules is likely to be more important during lesion initiation than during the later phase of rapid lesion growth. Both in experimental models of atherosclerosis and in human disease, infiltration of macrophages into the arterial intima constitutes one of the earliest cellular events in the development of atherosclerotic lesions.1Gerrity RG The role of the monocyte in atherogenesis. I. Transition of blood-borne monocytes into foam cells in fatty lesions.Am J Pathol. 1981; 103: 181-190PubMed Google Scholar, 2Joris I Zand T Nunnari JJ Krolikowski FJ Majno G Studies on the pathogenesis of atherosclerosis. I. Adhesion and emigration of mononuclear cells in the aorta of hypercholesterolemic rats.Am J Pathol. 1983; 113: 341-358PubMed Google Scholar, 3Stary HC The intimal macrophage in atherosclerosis.Artery. 1980; 8: 205-207PubMed Google Scholar Macrophages in the lesion may be derived either from cells already resident in the arterial wall4Miyata K Shimokawa H Kandabashi T Higo T Morishige K Eto Y Egashira K Kaibuchi K Takeshita A Rho-kinase is involved in macrophage-mediated formation of coronary vascular lesions in pigs in vivo.Arterioscler Thromb Vasc Biol. 2000; 20: 2351-2358Crossref PubMed Scopus (175) Google Scholar or from circulating monocytes that have undergone diapedesis. Because the mechanisms of cellular recruitment and/or activation are likely to differ depending on the source of the inflammatory cells, determining the relative contribution to lesion growth of cells from these two sources may have important implications in devising successful strategies to slow the growth of lesions. Although much convincing evidence demonstrates the importance of blood-borne monocytes in early lesion development,1Gerrity RG The role of the monocyte in atherogenesis. I. Transition of blood-borne monocytes into foam cells in fatty lesions.Am J Pathol. 1981; 103: 181-190PubMed Google Scholar, 5Rosenfeld ME Tsukada T Gown AM Ross R Fatty streak initiation in Watanabe heritable hyperlipidemic and comparably hypercholesterolemic fat-fed rabbits.Arteriosclerosis. 1987; 7: 9-23Crossref PubMed Google Scholar, 6Kim C-J Khoo JC Gillotte-Taylor K Li A Palinski W Glass CK Steinberg D Polymerase chain reaction-based method for quantifying recruitment of monocytes to mouse atherosclerotic lesions in vivo. Enhancement by tumor necrosis factor-α and interleukin-1β.Arterioscler Thromb Vasc Biol. 2000; 20: 1976-1982Crossref PubMed Scopus (41) Google Scholar the potential contribution of resident macrophages has been more difficult to assess. Experiments involving injection of labeled tracer monocytes can provide estimates for the rate of recruitment of circulating inflammatory cells but do not directly address the issue of mobilization of macrophages already present in arterial tissue. Moreover, alterations in adhesion molecule expression that can occur during monocyte isolation and labeling may modify the interaction between circulating monocytes and the vascular wall. The recent development of a polymerase chain reaction-based method of quantifying monocyte recruitment has shown promise of improved sensitivity and ease of quantitation compared to more traditional approaches such as labeling injected cells with radioisotopes or with fluorescent dyes,6Kim C-J Khoo JC Gillotte-Taylor K Li A Palinski W Glass CK Steinberg D Polymerase chain reaction-based method for quantifying recruitment of monocytes to mouse atherosclerotic lesions in vivo. Enhancement by tumor necrosis factor-α and interleukin-1β.Arterioscler Thromb Vasc Biol. 2000; 20: 1976-1982Crossref PubMed Scopus (41) Google Scholar but this method has not yet been adapted to the purpose of measuring resident macrophage recruitment. A recent study in which adventitial macrophages were fluorescently labeled in vivo by direct application of a dye solution provided evidence of a possible role for adventitial macrophage recruitment in the development of porcine coronary lesions.4Miyata K Shimokawa H Kandabashi T Higo T Morishige K Eto Y Egashira K Kaibuchi K Takeshita A Rho-kinase is involved in macrophage-mediated formation of coronary vascular lesions in pigs in vivo.Arterioscler Thromb Vasc Biol. 2000; 20: 2351-2358Crossref PubMed Scopus (175) Google Scholar In the present work, we have developed a novel approach to assess the relative contribution of resident versus circulating inflammatory cells to the development of macrophage-rich arterial lesions in the apoE knockout (KO) mouse using bone marrow transplantation (BMT). We have taken advantage of naturally occurring allelic variants of the mouse common leukocyte antigen (CD45 or Ptprc) to distinguish between host- and donor-derived white blood cells (WBCs) both in blood and in macrophage-rich carotid lesions. CD45, a transmembrane glycoprotein having intracellular tyrosine phosphatase activity,7Charbonneau H Tonks NK Walsh KA Fischer EH The leukocyte common antigen (CD45): a putative receptor-linked protein tyrosine phosphatase.Proc Natl Acad Sci USA. 1988; 85: 7182-7186Crossref PubMed Scopus (374) Google Scholar is expressed ubiquitously by nonerythroid hematopoietic cells. Using specific antibodies to two CD45 isoforms, we have been able to differentiate tissue-resident (host-derived) inflammatory cells from blood-borne (bone marrow- or donor-derived) cells in developing carotid lesions. Vascular cells produce a number of adhesion molecules, including intercellular adhesion molecule (ICAM)-1, vascular cell adhesion molecule(VCAM)-1, and P-selectin, which are thought to play a role in the recruitment of inflammatory cells to developing atherosclerotic lesions.8Patel SS Thiagarajan R Willerson JT Yeh ETH Inhibition of α4 integrin and ICAM-1 markedly attenuate macrophage homing to atherosclerotic plaques in apoE-deficient mice.Circulation. 1998; 97: 75-81Crossref PubMed Scopus (157) Google Scholar, 9Iiyama K Hajra L Iiyama M Li H DiChiara M Medoff BD Cybulsky MI Patterns of vascular cell adhesion molecule-1 and intercellular adhesion molecule-1 expression in rabbit and mouse atherosclerotic lesions and at sites predisposed to lesion formation.Circ Res. 1999; 85: 199-207Crossref PubMed Scopus (549) Google Scholar, 10Ramos CL Huo Y Jung U Ghosh S Manka DR Sarembock IJ Ley K Direct demonstration of P-selectin and VCAM-1-dependent mononuclear cell rolling in early atherosclerotic lesions of apolipoprotein E-deficient mice.Circ Res. 1999; 84: 1237-1244Crossref PubMed Scopus (231) Google Scholar, 11Cybulsky MI Iiyama K Li H Zhu S Chen M Iiyama M Davis V Gutierrez-Ramos J-C Connelly PW Milstone DS A major role for VCAM-1, but not ICAM-1, in early atherosclerosis.J Clin Invest. 2001; 107: 1255-1262Crossref PubMed Scopus (953) Google Scholar To assess whether recruitment of resident and circulating WBCs may depend differently on presentation of adhesion molecules by vascular cells, we have also examined the time course and spatial distribution of ICAM-1 and VCAM-1 expression in carotid lesions in relation to inflammatory cell infiltration. Monoclonal antibodies (mAbs) against mouse CD45.1 (clone A20), CD45.2 (clone 104), CD31 (PECAM-1; clone MEC 13.3), CD54 (ICAM-1; clone 3E2), CD106 (VCAM-1; clone 429), and Mac-3 (clone M3/84) were obtained from BD PharMingen (San Diego, CA). Nile Red and Alexa Fluor 488-streptavidin were purchased from Molecular Probes (Eugene, OR). Rhodamine Red X-conjugated secondary antibodies were from Jackson ImmunoResearch (West Grove, PA). Monoclonal rat anti-bromodeoxyuridine (BrdU) was purchased from Abcam, Ltd. (Cambridge, UK). Polyclonal rabbit anti-human CD3ε that cross-reacts with mouse T lymphocytes and monoclonal mouse anti-smooth muscle α-actin (clone 1A4) were from Sigma Chemical Co. (St. Louis, MO). Injectable busulfan (Busulfex) was obtained from Orphan Medical (Minnetonka, MN). Custom primers for polymerase chain reaction were prepared by Invitrogen (Rockville, MD). An atherogenic diet containing 1.25 wt% cholesterol, 0.5 wt% cholate, and 35 kcal% fat was purchased from Research Diets (New Brunswick, NJ). ApoE KO mice in the C57BL/6 background (B6.129P2-Apoetm1Unc) and mice in the same background homozygous for the CD45.1 alloantigen (B6.SJL-PtprcaPep3b/BoyJ) were purchased from Jackson Laboratories (Bar Harbor, ME). ApoE KO mice homozygous for the CD45.1 alloantigen (ApoE PepBoys) were obtained by crossbreeding the two strains. These mice were confirmed as apoE KOs by polymerase chain reaction of genomic DNA. Mouse genomic DNA was isolated from 1-cm tail samples using the Wizard Genomic DNA kit (Promega, Madison, WI). ApoE KO genotyping was performed using the primer set recommended by the developers of this strain.12Piedrahita JA Zhang SH Hagaman JR Oliver PM Maeda N Generation of mice carrying a mutant apolipoprotein E gene inactivated by gene targeting in embryonic stem cells.Proc Natl Acad Sci USA. 1992; 89: 4471-4475Crossref PubMed Scopus (742) Google Scholar Phenotypic analysis of CD45 alloantigen expression was performed by flow cytometry of peripheral blood WBCs as described below. Groups of CD45.1 apoE KO recipient mice were transplanted with bone marrow obtained from CD45.2 apoE KO donor mice. Donor mice and recipient mice were sex- and age-matched. Before BMT, recipient mice were injected intraperitoneally with 20 μg of busulfan/g body weight for 4 consecutive days to ablate the host bone marrow.13Yeager AM Shinn C Pardoll DM Lymphoid reconstitution after transplantation of congenic hematopoietic cells in busulfan-treated mice.Blood. 1991; 78: 3312-3316PubMed Google Scholar Bone marrow was harvested by flushing the femurs and tibias of donor mice with RPMI 1640 supplemented with 1% fetal bovine serum, 1% l-glutamine, and penicillin/streptomycin (transplant medium). Harvested bone marrow cells were washed twice with the same medium, diluted to a final concentration of 2.5 × 107 cells/ml, and injected into recipient mice via the retro-orbital venous sinus 18 to 24 hours after the final busulfan injection. The extent of donor bone marrow engraftment was assessed at 2 and 6 weeks after transplant by flow cytometric analysis of peripheral blood WBCs. For flow cytometric analysis, peripheral blood WBCs were isolated by gravity sedimentation of whole blood on 3% dextran in Hanks' balanced salt solution followed by red blood cell lysis by hypotonic shock. The WBCs were resuspended in fluorescence-activated cell sorting (FACS) staining medium (phenol red-free Hanks' balanced salt solution supplemented with 6% fetal bovine serum and 0.01 mol/L Na2-ethylenediaminetetraacetic acid). Isolated peripheral WBCs were stained for 30 minutes at 4°C in the dark with fluorescein isothiocyanate-labeled anti-mouse CD45.2 and R-phycoerythrin-labeled anti-mouse CD45.1 (1:100) before FACS analysis, then washed once with FACS staining medium, and resuspended in the same medium. Samples were analyzed by flow cytometry on a Becton-Dickinson FACSCalibur (Becton-Dickinson, Mountain View, CA). Between 5 × 105 and 12 × 105 total events were collected for analysis of engraftment of each transplanted mouse. Flow cytometric data were gated to exclude residual red blood cells and cell aggregates. Fractional engraftment was calculated as (CD45.2-positive WBCs)/(CD45.2-positive WBCs + CD45.1-positive WBCs) × 100%. Approximately 8 weeks after BMT, formation of arterial lesions was induced in recipient mice by ligation of the left common carotid artery according to our previously published method14Godin D Ivan E Johnson C Magid R Galis ZS Remodeling of carotid artery is associated with increased expression of matrix metalloproteinases in mouse blood flow cessation model.Circulation. 2000; 102: 2861-2866Crossref PubMed Scopus (178) Google Scholar and the mice were placed on an atherogenic diet. Groups of four to eight mice were sacrificed by means of CO2 asphyxiation after 3, 7, or 14 days on diet. The 0-day group consisted of mice that had received BMT but that had not been ligated. For analysis of cellular proliferation in carotid lesions, groups of three to four mice at each time point were injected intraperitoneally with the thymidine analog 5-bromo-2′-deoxyuridine (BrdU) (250 μl of 10 mg/ml in normal saline) at 12 hours and 1 hour before sacrifice. Blood samples were obtained from the retro-orbital venous sinus for analysis of total plasma cholesterol using the Infinity Cholesterol Reagent (Sigma Diagnostics). After sacrifice, the vasculature was cleared of blood by brief pressure perfusion with normal saline via the left ventricle, with outflow through the severed vena cava. Tissue samples (spleen, liver, lung, carotids) were dissected out, embedded in OCT medium, and frozen in liquid nitrogen with 2-methylbutane as heat transfer fluid. Both carotids were removed together with the aortic arch and embedded in a vertical orientation. All animal protocols were approved by the Emory University Institutional Animal Care and Use Committee. Frozen sections were cut at 7 μm and collected on Superfrost Plus slides (Fisher Scientific, Pittsburgh, PA). We sectioned the entire length of each carotid artery from its origin at the aortic arch to the vicinity of the ligation. Serial sections for immunohistochemistry were collected in groups of seven with intervals of 140 μm between the first section in each group. To determine which groups of serial sections encompassed the apex of the lesion, one section out of each group of 40 was examined by phase contrast microscopy. Serial frozen sections of carotid lesions were fixed in ice-cold acetone and stained with biotinylated mAbs to CD45.1 or CD45.2 (1:20 dilution) followed by Alexa Fluor 488-labeled streptavidin to determine the distribution and relative abundance of host-type and donor-type WBCs, respectively. Nuclei were counterstained with Hoechst 33258. Sections from carotid lesions of apoE PepBoys that had not undergone BMT were stained identically for comparison. To assess the cellular composition of lesions in the transplanted mice, additional serial sections were immunostained with cell type-specific antibodies including anti-Mac3 for monocytes/macrophages, anti-smooth muscle α-actin for smooth muscle cells (SMCs), anti-CD3 for T lymphocytes, and anti-CD31 for endothelial cells. Some frozen sections were fixed in 4% paraformaldehyde and stained with Nile Red to visualize the distribution of lipids in the lesions. Adhesion molecule expression was evaluated by staining acetone-fixed frozen sections with primary mAbs to ICAM-1 (1:50 dilution) or VCAM-1 (1:50 dilution) followed by Rhodamine Red X-labeled secondary antibodies for detection by immunofluorescence microscopy. Cell proliferation in carotid lesions was analyzed by staining paraformaldehyde-fixed frozen sections using a rat mAb to BrdU (1:20) followed by detection with a Rhodamine Red X-labeled anti-rat IgG. Some sections were stained simultaneously with anti-BrdU and biotinylated anti-CD45.1 or anti-CD45.2 mAbs for analysis of host- and donor-specific WBC proliferation. Total intimal cell numbers were determined by semiautomated image analysis of Hoechst-stained nuclei. Intimal proliferation index was defined as (number of BrdU-stained intimal nuclei)/(total number of intimal nuclei) × 100%. For morphometric analysis, frozen sections obtained from the apex of the carotid lesion were stained with anti-CD31 to visualize the luminal boundary as defined by the endothelium. Luminal area was measured by tracing this boundary. The elastic laminae were visualized by means of their autofluorescence using a fluorescein isothiocyanate filter set. Internal elastic lamina (IEL) area was measured by tracing the contour of the IEL. Lesion (intimal) area was calculated as the difference between IEL area and luminal area. External elastic lamina (EEL) area was measured as the area encompassed by the outermost elastic lamina. Images were acquired using a Zeiss Axioskop fluorescence microscope equipped with a Photonic Science cooled CCD camera. All image analysis was performed using ImagePro Plus software (Media Cybernetics, Silver Spring, MD). Student's t-test was used for comparison of means between groups at each time point. A value of P < 0.05 was considered significant. We successfully established a strain of apoE KO mice homozygous for the rare CD45.1 (Ptprca) allele of the mouse common leukocyte antigen. The genotype (apoE KO) and the phenotype (CD45.1 homozygote) of these mice were confirmed by polymerase chain reaction (data not shown) and by FACS analysis of peripheral WBCs, respectively (Figure 1A). Engraftment of bone marrow transplanted from apoE KO CD45.2 homozygous donors to apoE KO CD45.1 homozygous recipients after busulfan conditioning followed a uniform time course as measured by flow cytometry of peripheral WBCs. By 2 weeks after transplant, FACS analysis indicated that 63 ± 14% (n = 33) of circulating WBCs were donor-derived (CD45.2-positive). Donor-derived hematopoietic engraftment increased steadily throughout time to a value of 84 ± 7% (n = 37) donor-type cells at 6 weeks after transplant (Figure 1B), after which the values approached a plateau. Chimerism of peripheral WBCs at 8 weeks (81 ± 9%, n = 4) was not significantly different from that at 6 weeks. In this study, arterial lesion development was initiated by carotid ligation on average 8 weeks after BMT to ensure that donor-type cells predominated in the circulation. We measured total plasma cholesterol levels in apoE KO mice that had received BMTs and compared them to levels in nontransplanted apoE KO mice to confirm that BMT in itself did not alter the response to an atherogenic diet. Plasma cholesterol levels were significantly elevated over baseline by 3 days on diet. After 14 days of atherogenic diet, the plasma cholesterol level was not significantly different in transplanted apoE KO mice than in nontransplanted mice (1700 ± 570 mg/dl, n = 9, versus 1830 ± 460 mg/dl, n = 5). Plasma cholesterol levels in transplanted apoE KO mice fed a standard chow diet also were not significantly different from those in nontransplanted mice on the same diet (data not shown). Carotid lesions developed rapidly in the ligated arteries of ApoE KO transplant mice fed an atherogenic diet (Figure 2). No lesions were present in nonligated carotid arteries of the transplanted mice. By 3 days after ligation, inflammatory cell recruitment was evident in some but not all transplanted mice as a partial lining of adherent WBCs at the luminal surface. By 7 days after ligation, all transplanted mice had developed intimal lesions (Figure 2A). Lesion area increased dramatically between 7 and 14 days after ligation (Figure 2B), leading to nearly complete occlusion of the vessel lumen (Figure 2C). Immunohistochemical analysis of host and donor WBC distribution in carotid artery lesions of ApoE KO transplant mice showed that the majority of inflammatory cells in the lesions at 7 and 14 days after ligation were donor-derived (CD45.2-positive), as demonstrated by serial sections (Figure 3). At 14 days, 85 ± 8% (n = 4) of intimal WBCs were donor-derived, as measured by digital image analysis of immunostained serial sections. Few host-derived WBCs were present in the developing lesions, although some were evident in the adventitia of the ligated arteries. Cell type-specific immunohistochemical staining with antibody to Mac-3 demonstrated that the majority of inflammatory cells present in the carotid lesions of ligated, transplanted mice were monocyte/macrophages (Figure 4). A few CD3-positive T lymphocytes were present as well (data not shown). At 7 and 14 days after ligation, macrophages in the lesion contained substantial amounts of lipid, indicative of their transition into foam cells. Double labeling with antibodies to Mac-3 and CD45.2 revealed that the distribution of host- and donor-derived macrophages in the vessel changed during the course of lesion development (Figure 4). As expected, control animals that had not undergone BMT or carotid ligation showed no staining for donor-type macrophages. Host-type macrophages were identified only in the adventitial layer of the vessel. In transplanted mice before initiation of lesion development, adventitial macrophages comprised a mixture of host- and donor-derived cells. By 3 days after ligation, donor-type monocyte/macrophages had begun to adhere to the luminal endothelium. At 14 days, the majority of macrophages and macrophage-derived foam cells in the neointima of the left carotid were of donor origin, whereas examination of the nonligated, contralateral artery at the same time point revealed a mixture of host- and donor-type macrophages in the adventitia, similar to that observed in the left carotids before ligation. A quantitative analysis revealed that, before ligation, ∼55 ± 3% (n = 4) of adventitial WBCs originated from the donor bone marrow. The adventitial distribution of host- and donor-type WBCs was distinctly different from that in the circulation, where donor-derived cells constituted 78 ± 11% (n = 4) of circulating WBCs at 6 weeks after transplant in the same mice (P = 0.013, two-tailed paired t-test). Thus, before the initiation of atherosclerotic lesions, host-type cells accounted for a significantly greater fraction of tissue-resident, adventitial macrophages than of circulating monocytes. Intimal proliferation index increased significantly between 7 and 14 days after ligation, from 3.7 ± 2.6% (n = 3) of intimal cells to 14.8 ± 2.8% (n = 4). Compared to baseline values, the total number of proliferating cells in the neointima was significantly elevated at 14 days after ligation (Table 1). Many of these proliferating intimal cells stained positively for CD45.2, establishing their identity as donor-derived WBCs (Figure 5). Proliferating donor-derived leukocytes were observed throughout the neointima, with no apparent spatial preference (Figure 5; additional data not shown).Table 1Intimal Proliferation in ApoE Transplant Mice after Carotid LigationTime on diet, daysBrdU-labeled intimal cells, mean ± SEM (n)00.2 ± 0.2 (4)37.0 ± 3.6 (4)77.3 ± 3.4 (3)1487.2 ± 18.0*P < 0.05 relative to day 0. (4)* P < 0.05 relative to day 0. Open table in a new tab To evaluate possible routes of inflammatory cell recruitment, we examined the time course of adhesion molecule expression in the ligated carotids by means of immunohistochemical staining for ICAM-1 and VCAM-1. The time course of expression and the spatial localization of ICAM-1 were distinctly different from those of VCAM-1 (Figure 6). Before the initiation of lesions and at 3 days after ligation (Figure 6), VCAM-1 was expressed at the luminal boundary of the vessel, where it co-localized with endothelial cells identified by CD31 staining. By 7 days after ligation, however, VCAM-1 expression had disappeared from the endothelium and had shifted to the media, where VCAM-1 staining co-localized with smooth muscle α-actin. In contrast, the endothelium expressed ICAM-1 throughout the course of carotid lesion development up to 14 days after ligation, although expression at later time points was diminished compared to baseline levels. Adventitial ICAM-1 expression was evident by 3 days after ligation and increased during the course of lesion progression. In addition, ICAM-1 staining was detected on cells in the deeper layers of the neointima during the later stages of lesion development. Bone marrow transplantation in the apoE KO and LDL-receptor KO mouse models has been well established as a method for examining the influence of protein expression by macrophages on the development of atherosclerotic lesions.15Boisvert WA Spangenberg J Curtiss LK Treatment of severe hyper-cholesterolemia in apolipoprotein E-deficient mice by bone marrow transplantation.J Clin Invest. 1995; 96: 1118-1124Crossref PubMed Scopus (183) Google Scholar, 16Fazio S Babaev VR Murray AB Hasty AH Carter KJ Gleaves LA Atkinson JB Linton MF Increased atherosclerosis in mice reconstituted with apolipoprotein E null macrophages.Proc Natl Acad Sci USA. 1997; 94: 4647-4652Crossref PubMed Scopus (248) Google Scholar, 17Accad M Smith SJ Newland DL Sanan DA King Jr, LE MacRae L Fazio S Farese RV Massive xanthomatosis and altered composition of atherosclerotic lesions in hyperlipidemic mice lacking acyl CoA:cholesterol acyltransferase 1.J Clin Invest. 2000; 105: 711-719Crossref PubMed Scopus (207) Google Scholar Previous studies have shown that transplantation of syngeneic wild-type bone marrow into apoE KO recipients retards atherosclerotic lesion growth in these mice, partially rescuing the phenotype through production of apoE by donor-derived macrophages.15Boisvert WA Spangenberg J Curtiss LK Treatment of severe hyper-cholesterolemia in apolipoprotein E-deficient mice by bone marrow transplantation.J Clin Invest. 1995; 96: 1118-1124Crossref PubMed Scopus (183) Google Scholar In the present study, however, we were interested in using the difference between donor- and host-derived cells primarily as a means to track inflammatory cell migration into developing lesions in vivo. We reasoned that this approach could be used to resolve definitively the longstanding issue of whether intimal macrophages in developing atherosclerotic lesions originate primarily from tissue-resident precursors or from circulating monocytes. We therefore aimed to develop a model in which BMT itself would have minimal effect on the course of atherosclerotic lesion development compared to that observed in nontransplanted apoE KO mice. In the work that we report here, we have demonstrated the utility of a novel approach to track the recruitment of inflammatory cells into developing atherosclerotic lesions in the mouse carotid artery in vivo, using differences in CD45 (Ptprc) alleles to distinguish host- and donor-derived WBCs in a BMT model. This approach offers several advantages over protocols in which WBCs are labeled ex vivo and re-injected. First, the label (ie, antigenic difference between CD45.1 and CD45.2) is permanent and does not diminish in intensity in succeeding generations of cells descended from the original donors, unlike fluorescent dye labels that are diluted at each cell division. Secondly, our protocol avoids artifacts resulting from inadvertent activation of WBCs during isolation, labeling, and re-injection. The donor WBCs that function as tracers in this model have not been genetically manipulated in any manner that might alter their functionality. The difference between the Ptprca (CD45.1) and Ptprcb (CD45.2) alleles amounts to five amino acid changes in the extracellular region of the protein,18Zebedee SL Barritt D Epstein R Raschke WC Analysis of Ly5 chromosome 1 position using allelic differences and recombinant inbred mice.Eur J Immunogenet. 1991; 18: 155-163Crossref PubMed Scopus (9) Google Scholar which confer altered antigenicity but have no other known effects on leukocyte function. The more common Ptprcb (CD45.2) allele occurs in b
Referência(s)