Respiratory Disease

Total Page:16

File Type:pdf, Size:1020Kb

Respiratory Disease r Volume 132 Number 4 October 1985 ISSN 0003-0805 AMERICARespiratorN REVIEW OF y Disease OFFICIAL JOURNAL OF THE AMERICAN THORACIC SOCIETY MEDICAL SECTION OF THE AMERICAN LUNG ASSOCIATION 1382 Pulmonary Morphologist — Opportunity for Ph.D. or M.D. for ap• tice, teaching affiliations. Proficient all procedures. Available now pointment as Assistant or Associate Professor (research) in the In• or July 1986. Reply Box 582. stitute for Environmental Medicine and the Department of Pathol• ogy and Laboratory Medicine at the University of Pennsylvania Postdoctoral Research Fellowships in Lung Research for 1985-86 School of Medicine. Successful candidate will collaborate with es• and 1986-87 available in the University of California, Davis (UCD) tablished investigators in respiratory physiology/experimental Interdisciplinary Pulmonary Disease Research Group. Ph.D., M.D., pathology and will develop an independent research program in or DVM required. Ongoing research areas include nutritional aspects respiratory cell biology. Experience with electron microscopy is es• of lung disease, alveolar macrophage cytochemistry, respiratory gly• sential. Ample space, funding opportunities, and state-of-the-art coprotein biosynthesis and metabolism, lung collagen and elastin, facilities are available. Deadline for applications is December 31, lung liposomes and lipoprotein metabolism, airway nerves and blood 1985. Interested applicants should send C.V., statement of research supply, relationships of xenobiotic metabolism to pulmonary cyto• interests, and names of three references to Aron B. Fisher, M.D., toxicity, mechanism of respiratory epithelial differentiation, respira• Director, Institute for Environmental Medicine, Chairman, Pulmo• tory tract permeability, and inhalation toxicology. Eight UCD faculty nary Morphology Search Committee, University of Pennsylvania with research activities in lung disease involved in fellowship train• School of Medicine/G2, Philadelphia, PA 19104. The University ing program. Send resume to: Dr. C. E. Cross, Division of Pulmo• of Pennsylvania is an equal opportunity/affirmative action employer. nary Medicine, 4301 "X" St., University of California, Davis Medi• cal Center, Sacramento, CA 95817. Equal Opportunity/Affirma• Pulmonologist: Board certified or eligible to join expanding 2-man tive Action Institution. group in midwest city with large university. Must be proficient in all aspects of pulmonary and critical care medicine and be willing Practice for sale: Pulmonary and Internal Medicine. Active prac• to do some internal medicine. Please reply with C.V. to Box 575. tice for 11 years. Nice Chicago suburban location. Practice includes office building, fully equipped office. Will introduce. Reply to Box 584. Pulmonary physician sought to join pulmonary division of a major Canadian university hospital. Candidate must be experienced and Pulmonologist —To join 7 internists in 20-man multispeciality group. capable of conducting independent clinical or basic research. Reply Must be able to practice excellent general internal medicine as well. Box 583. City of 32,000 with 2 hospitals, serving area of 200,000. No pulmo- nologist in area. Attractive family environment, nearby lake, con• Pulmonologist/Internist, require BE/BC-pulmonary. N.Y.C. sub• venient to Twin Cities. Send C.V. to Administrator, Park Clinic, 890 urb, active ICU, office consultation, 80% pulmonary, PVT prac• North Eisenhower, Mason City, IA 50401. Necrology (April-October 1985) Warde B. Allan, M.D. Joseph T. Eagan, M.D. George C. Owen, M.D. Garrison, Maryland Oneonta, New York Brookfield, Wisconsin Kelly M. Berkley, M.D. Norma C. Furtos, M.D. I. Ellis Rudman, M.D. Phoenix, Arizona Escondido, California New York, New York Thomas C. Black, M.D. Joseph C. Hart, M.D. Cecil L. Schultz, M.D. Temple, Texas Poughkeepsie, New York Venice, Florida William Brueggmann, M.D. Peter P. Kozak, Jr., M.D. Clarence Sharp, M.D. Mainville, Ohio Santa Ana, California Jacksonville, Florida Kenneth G. Bulley, M.D. Wiliam H. McCain, M.D. John Srail, M.D. Fort Myers, Florida Springfield, Illinois Tacoma, Washington Henry A. Christian, M.D. Walter H. Modarelli, M.D. George W. Ware, M.D. Whiting, New Jersey Leonia, New Jersey Bowie, Maryland E. Leslie Chusid, M.D. Valerie J. Molzahn, M.D. William L. Weintraub, M.D. New York, New York Redlands, California Totowa, New Jersey Royal S. Davis, M.D. William R. Murlin, M.D. New Rochelle, New York Salem, Oregon INDEX-AUTHORS ABEL, JEFFREY, 159 BIXLER, EDWARD O., 972 CHIESURA-CORONA, P., 1010 ABERNATHY, ROBERT S., 931 BLEECKER, EUGENE R., 220 CHILOSI, M., 400 ACKERMAN, STEVEN J., 981 BOAT, THOMAS F., 770 CHOLLET-MARTIN, SYLVIE, 836 ACOCELLA, GIANNI, 510, 1268, 1274 BOBEY, DAVID G., 409 CHOU, JEAN, 382 ADAMSON, DAVID, 916 BONNEY, THOMAS B., 1174 CHRISTENSEN, LOUISE, 409 ADKINSON, N. FRANKLIN, JR., 99, 367 BORGEN, LOWELL, 1194 CHRISTENSEN, T. G., 362 AGOSTINI, C, 400 BOUCHER, RICHARD C, 311, 1281 CHRISTIANS DAVID C, 120, 1371 AHMED, TAHIR, 839 BOUDIER, CHRISTIAN, 913 CHRISTMAN, JOHN W., 152, 393 AHRENS, JOAN, 752 BOUSHEY, H. A., 690 CHURCH, MARTIN K., 986 ALBERT, RICHARD K., 623, 963 BOXER, LAURENCE A., 1288 CHURG, ANDREW, 922 ALLEN. DARREL, 590 BRADLEY, T. D., 211 CIPRIANI, A., 400 ALLEN. JULIAN L., 343 BRADSHER, ROBERT W., JR., 931 CLARK, JOHN C, 1181 ALTOSE, MURRAY D., 800, 954 BRAIN, JOSEPH D., 606 CLAUDE, JEAN-ROGER, 818 AMEND, PHILIPPE, 504 BRAUN, NORMA M. T., 42 CLAUSEN, JACK L., 685 ANDERSON, R., 1049 BREUER, RAPHAEL, 362, 1155 CLAYTON, JAMES, 321 ANDO, MASAYUKI, 299 BRIDGES, RAYMOND B., 1162 CLOZEL, JEAN-PAUL, 504 ANDREADIS, NICHOLAS, 1344 BRODY, JEROME S., 905, 1307 COALSON, JACQUELINE J., 358, 1262 ANGUS, G. ELSPETH, 894 BROWN, I. G., 211 COHEN, ALLEN B., 1098 ANTHONISEN, NICHOLAS R., 871 BROWN, STEPHEN E., 960 COHEN, BERNICE H., 115 ANTTINEN, HENRIK, 536 BRUCE, MARGARET C, 529 COLE, PHILIP, 1229 ANZAR, UTE T., 619 BRUESKE, DE WANE A., 186 COLLIER, ALBERT M., 875 ARAKI, SHUKURO, 299 BUCKNER, C. K., 305 COLMAN, ROBERT W., 1098 ARBABIAN, MARTIN, 1194 BUIST, A. SONIA, 821, 1186 CONNAUGHTON, JOHN J., 206 ARMOUR, C. L., 30 BURKI, N. K., 1210 CONNELLAN, S. J., 148 ASHTON, JULIET, 564, 1262 BURNS, STEPHEN R., 109 CONOLLY, MATTHEW E., 12 ASTIER, ALAIN, 748 BURRI, PETER H., 777 CONTI, ROBERT, 510 ATASSI, KIN AN, 1118 BURSTIN, S., 133 CONWAY, W., 520 AUSTEN, FRANK, 1204 BUSSE, WILLIAM W., 305, 1194 COOK, JAMES L., 1246 AVOL, EDWARD L., 619 BUTKA, BRENDA J., 931 COONEY, THOMAS P., 596 BACHMANN, MARLIES, 479 BUTLER, JOHN E., 623, 963, 1027 CORDONNIER, CATHERINE, 748, 1118 BALDWIN, STEPHEN R., 1288 BYE, PETER T. P., 236 COREY, E. J., 1204 BALK, ROBERT A., 929 CADIEUX, ROGER J., 972 CORN, CAROLYN J., 143 BALLAS, ZUHAIR K., 77 CALAFIORE, DOROTHY C, 261 CORWIN, R. WILLIAM, 576 BANNER, ARTHUR S., 993 CALDWELL, JAMES, 623, 963 COSIO, MANUEL G., 894, 1366 BARNES, PETER J., 541, 1019 CALLEN, PETER W., 1253 COTTON, CALVIN U., 1281 BARON, ROBERT B., 737 CALORE, J. D., 362, 1155 COVER, D., 1233 BARRY, BRENDA E., 548 CALVERLEY, P. M. A., 86 COVERT, DAVID S., 648 BARTER, S. J., 148 CAMPBELL, D. A., 1300 CRAIG, KENNETH C, 1071 BARTLETT, DONALD, JR., 216, 1242 CANTOR, JEROME O., 640 CRANZ, DIANE L., 556 BASS, JOHN B., 379 CARLI, GIULIO, 806 CRAPO, JAMES D., 548 BASSET, FRANCOISE, 836 CARLONE, NICOLA A., 1268, 1274 CRAWFORD, JACK T., 386 BASSET, GUY, 880 CARRICO, C. JAMES, 485 CRITCHLEY, JULIAN A. J. H., 206 BATES, JOSEPH H., 386 CARSTAIRS, J. R., 541 CROWLE, A. J., 742 BATTER, WERNER, 1060 CARTIER, ANDRE, 644, 848 CRUZ, EDGARDO, 48 BAUGHMAN, ROBERT P., 390 CASTAING, YVES, 332 CRYSTAL, RONALD, 821 BAUMANN, HANS R., 1060 CASTELLAN, ROBERT M., 1139 CUFFINI, ANNA MARIA, 1268, 1274 BEASLEY, PAT, 976 CATANESE, ANTHONY, 362, 1155 CULPEPPER, JUDITH A., 1075 BEATY, TERRI H., 115 CATTERALL, J. R., 86 CULVER, BRUCE H., 788 BECKER, CAROLINE, 175 CAUTHEN, GEORGE M., 125, 516 CUNNINGHAM, D. A., 148 BECKLAKE, MARGARET R., 1127 CAVALLO, GIORGIO, 1268 CURLEY, FREDERICK J., 1130 BEKERMAN, CARLOS, 746 CEDERBAUMS, DAINA, 582 CUSHLEY, MICHAEL J., 1 BEN-BASSAT, M., 602 CERVANTES, PIERRE, 712 CUSTER, JOSEPH R., 326 BENFIELD, JOHN R., 434 CHANG, H. K., 104, 350 DAL VECCHIO, L., 1010 BENGALI, ZAKIR, 182 CHAN-YEUNG, MOIRA, 814 DANIEL, E. E., 272, 865 BENOIT, GUY, 748 CHAPARAS, SOTIROS D., 175 DARGENT, FRANCOISE, 479 BENSON, KIM N., 472 CHAPMAN, HAROLD A., JR., 569 DAUBER, JAMES H., 152 BEREND, NORBERT, 582 CHAPMAN, K. R., 845 DAUPHINEE, BETH, 12 BERGER, LORENZ C, 777 CHAPMAN, ROBERT S., 261, 875 DAVIS, GERALD S., 393 BERGOFSKY, EDWARD H., 633 CHATHAM, MARIE D., 36 DAVIS, ROBIN L., 761 BERLINER, S., 602 CHAUSOW, ALAN, 746 DEAL, E. CHANDLER, JR., 1214 BERNAUDIN, JEAN-FRANCOIS, 748, 1118 CHECK, IRENE J., 65 DEARBORN, DORR G., 429, 770 BERRY, DAVID D., 500, 1313 CHENG, C, 311 DEGRAFF, ARTHUR C, JR., 858 BICE, DAVID E., 647, 661 CHERNIACK, NEIL S., 1214 DELACROIX, D. L., 829 BIETH, JOSEPH G., 524, 818, 913 CHERNIACK, REUBEN M., 582, 590 DELANEY, MORGAN D., 1087 BIGBY, TIMOTHY D., 590 CHERNICK, VICTOR, 16 DE MARZO, N., 1010 1383 1384 AUTHOR INDEX DEMLING, ROBERT H., 1257 FRASER, IAN M., 766 HARGREAVE, F. E., 272, 865 DERKSEN, FREDERIK, 1066 FREDBERG, JEFFREY J., 343 HARTEMANN, DENISE, 504 DE TROYER, ANDRE, 53, 793 FRICK, OSCAR L., 292 HARTIALA, JAAKKO, 292 DHILLON, DHARAM P., 926 FUKUDA, TAKESHI, 981 HASSELBLAD, VICTOR, 261 DIAMOND, LOUIS, 885 FULLER, RICHARD K., 770 HAYES, EDWARD E., 367 DICK, E. C, 305 GAGNON, GILLES, 644 HEBEL, J. RICHARD, 36 DIERKS, STEVE E., 1027 GALLINA, CLAUDIA, 712 HECHTMAN, HERBERT, 1257 DI GIACOMO, G. R., 1010 GAMSU, GORDON, 1124, 1253 HEIFETS, LEONID B., 710, 1278 DILLARD, THOMAS A., 230 GANGADHARAM, PATTISAPU R. J., 1278 HEINRICHS, W. LEROY, 916 DIMARCO, ANTHONY F., 800 GANTER, BERNARDUS, 737 HELDT, GREGORY P., 339 DIMARCO, MARIANNE S., 800 GANZ, T., 901 HENDLEY, J. OWEN, 976 DI PEDE, FRANCESCO, 806 GASPAROTTO, G., 400 HENSON, JAN E., 152 DISE, CRAIG A., 191 GAIZY, JOHN T., 1281 HENSON, PETER M., 490, 590 DISTEFANO, SANDRA, 1106 GAULDIE, JACK, 82 HIBBERT, MARIENNE, 1223 DODSON, RONALD F., 143 GAUTHIER, RICHARD, 848 HIDA, W., 278, 671 DOHN, MICHAEL N., 390 GEFFROY, B.
Recommended publications
  • Oral Health and Respiratory Infection
    C LINICAL P RACTICE Oral Health and Respiratory Infection • Philippe Mojon, DMD, PhD • Abstract The oral cavity has long been considered a potential reservoir for respiratory pathogens. The mechanisms of infec- tion could be aspiration into the lung of oral pathogens capable of causing pneumonia, colonization of dental plaque by respiratory pathogens followed by aspiration, or facilitation by periodontal pathogens of colonization of the upper airway by pulmonary pathogens. Several anaerobic bacteria from the periodontal pocket have been isolated from infected lungs. In elderly patients living in chronic care facilities, the colonization of dental plaque by pulmonary pathogens is frequent. Notably, the overreaction of the inflammatory process that leads to destruc- tion of connective tissue is present in both periodontal disease and emphysema. This overreaction may explain the association between periodontal disease and chronic obstructive pulmonary disease, the fourth leading cause of death in the United States. These findings underline the necessity for improving oral hygiene among patients who are at risk and those living in long-term care institutions. MeSH Key Words: aged; periodontal diseases/epidemiology; pneumonia, aspiration/epidemiology; pneumonia, aspiration/ prevention & control © J Can Dent Assoc 2002; 68(6):340-5 This article has been peer reviewed. he anatomical continuity between the lungs and the different for the 2 types. CAP is a frequent illness, with an oral cavity makes the latter a potential reservoir of incidence rate estimated at about 8 cases per 1,000 inhabi- Trespiratory pathogens. Yet an infective agent must tants per year in industrialized countries. The mortality rate defeat sophisticated immunological and mechanical is about 7% in hospitalized patients.1 Streptococcus pneumo- defence mechanisms to reach the lower respiratory tract.
    [Show full text]
  • Diffuse Alveolar Hemorrhage Syndrome Secondary to Bocavirus
    Case report Diffuse alveolar hemorrhage syndrome secondary to bocavirus and rhinovirus infection in a pediatric patient Síndrome de hemorragia alveolar difusa secundaria a coinfección por Rhinovirus y Bocavirus en un paciente pediátrico Carlos Eduardo Reina1 , Sandra Patricia Concha2, Rubén Eduardo Lasso2, Fernando Bermúdez2, María Teresa Agudelo3 Abstract The diffuse alveolar hemorrhage syndrome is characterized by the presence of blood in the pulmonary alveolus from arterioles, venules and pulmonary Date correspondence: capillaries, as a consequence of the lesion of the alveolar wall and without an Received: February 20, 2015. endobronchial alteration. Its presentation includes a classic triad of hemopty- Revised: September 11, 2017. sis, anemia and diffuse alveolar infiltrates. It´s a rare but potentially fatal entity Accepted: October 31, 2017. and there are no clear data on its real incidence in the pediatric population. We present the case of a previously healthy pediatric patient, immunocompetent, How to cite: who presented diffuse alveolar hemorrhage syndrome with secondary venti- Reina CE, Concha SP, Lasso RE, latory failure. After discarding all possible etiologies, coinfection by Rhinovirus Bermudez F, Agudelo MT. Diffuse and human Bocavirus was detected through the polymerase chain reaction, alveolar hemorrhage syndrome determining them as causal factors of the event. Recently, viral infections secondary to Rhinovirus and have been postulated as causing serious lung disease, especially coinfec- Bocavirus coinfection in a tion in immunocompromised patients, in this case Rhinovirus and human pediatric patient. Rev CES Bocavirus; however there are no reports on the syndrome caused by these Medicina. 2018; 32(1): 53-60. viruses. Open access Keywords: Diffuse alveolar hemorrhage; Respiratory failure; Rhinovirus; © Derecho de autor Human Bocavirus.
    [Show full text]
  • Lipid–Protein and Protein–Protein Interactions in the Pulmonary Surfactant System and Their Role in Lung Homeostasis
    International Journal of Molecular Sciences Review Lipid–Protein and Protein–Protein Interactions in the Pulmonary Surfactant System and Their Role in Lung Homeostasis Olga Cañadas 1,2,Bárbara Olmeda 1,2, Alejandro Alonso 1,2 and Jesús Pérez-Gil 1,2,* 1 Departament of Biochemistry and Molecular Biology, Faculty of Biology, Complutense University, 28040 Madrid, Spain; [email protected] (O.C.); [email protected] (B.O.); [email protected] (A.A.) 2 Research Institut “Hospital Doce de Octubre (imasdoce)”, 28040 Madrid, Spain * Correspondence: [email protected]; Tel.: +34-913944994 Received: 9 May 2020; Accepted: 22 May 2020; Published: 25 May 2020 Abstract: Pulmonary surfactant is a lipid/protein complex synthesized by the alveolar epithelium and secreted into the airspaces, where it coats and protects the large respiratory air–liquid interface. Surfactant, assembled as a complex network of membranous structures, integrates elements in charge of reducing surface tension to a minimum along the breathing cycle, thus maintaining a large surface open to gas exchange and also protecting the lung and the body from the entrance of a myriad of potentially pathogenic entities. Different molecules in the surfactant establish a multivalent crosstalk with the epithelium, the immune system and the lung microbiota, constituting a crucial platform to sustain homeostasis, under health and disease. This review summarizes some of the most important molecules and interactions within lung surfactant and how multiple lipid–protein and protein–protein interactions contribute to the proper maintenance of an operative respiratory surface. Keywords: pulmonary surfactant film; surfactant metabolism; surface tension; respiratory air–liquid interface; inflammation; antimicrobial activity; apoptosis; efferocytosis; tissue repair 1.
    [Show full text]
  • Respiratory System
    RESPIRATORY SYSTEM Dept.Dept. ofof HistologyHistology andand EmbryologyEmbryology 周莉周莉 教授教授 Respiratory System Nose Pharynx Larynx Trachea Bronchus Lung NASAL CAVITY 1. Mucosa:epithelium and lamina propria 1.1 Vestibular Region: 1.2 Respiratory Region: pseudostratified ciliated columnar epithelium, mixture glands (nasal glands), abundant blood vessels and lymphoid tissue in lamina propria 1.3 Olfactory Region (1) Olfactory epithelium: pseudostratified ciliated columnar epithelium A. supporting cells B. olfactory cells C. basal cells (2) Lamina Propria: olfactory glands (serous type) Olfactory epithelium TRACHEA AND BRONCHUS Mucosa: Pseudostratified ciliated columnar epiothelium Lamina propia Submucosa:LCT Advantitia: cartilage tissue and CT 1. Mucosa 1.11.1 PseudostratifiedPseudostratified ciliatedciliated columnarcolumnar epitheliumepithelium (1)(1) ciliatedciliated cellscells (2)(2) gobletgoblet cellscells (3)(3) basalbasal cellscells (4)(4) brushbrush cellscells (5)(5) diffusediffuse neuroendocrineneuroendocrine cellscells (small(small granulegranule cells)cells) Tracheal Sueface (SEM) Pseudostratified ciliated columnar epithelium(LM) 1.21.2 LaminaLamina PropriaPropria ThickThick basementbasement membrane,membrane, CTCT,, immuneimmune cellscells 2.2. SubmucosaSubmucosa::LCTLCT TrachealTracheal glandsglands (( mixturemixture type)type),, mucousmucous barrierbarrier lymphoidlymphoid tissuetissue thethe effectseffects ofof sIgAsIgA Tracheal wall 3. Advantitia C- shaped rings of hyaline cartilage and LCT membrane portion:ligament rich in
    [Show full text]
  • Investigation on Microparticle Transport and Deposition Mechanics in Rhythmically Expanding Alveolar Chip
    micromachines Article Investigation on Microparticle Transport and Deposition Mechanics in Rhythmically Expanding Alveolar Chip Jun Dong 1,† , Yan Qiu 1,†, Huimin Lv 1, Yue Yang 2,* and Yonggang Zhu 2,* 1 School of Science, Harbin Institute of Technology, Shenzhen 518055, China; [email protected] (J.D.); [email protected] (Y.Q.); [email protected] (H.L.) 2 School of Mechanical Engineering and Automation, Harbin Institute of Technology, Shenzhen 518055, China * Correspondence: [email protected] (Y.Y.); [email protected] (Y.Z.) † These authors contributed equally to this work. Abstract: The transport and deposition of micro/nanoparticles in the lungs under respiration has an important impact on human health. Here, we presented a real-scale alveolar chip with movable alveolar walls based on the microfluidics to experimentally study particle transport in human lung alveoli under rhythmical respiratory. A new method of mixing particles in aqueous solution, instead of air, was proposed for visualization of particle transport in the alveoli. Our novel design can track the particle trajectories under different force conditions for multiple periods. The method proposed in this study gives us better resolution and clearer images without losing any details when mapping the particle velocities. More detailed particle trajectories under multiple forces with different directions in an alveolus are presented. The effects of flow patterns, drag force, gravity and gravity directions are evaluated. By tracing the particle trajectories in the alveoli, we find that the drag force contributes to the reversible motion of particles. However, compared to drag force, the gravity is the decisive factor for particle deposition in the alveoli.
    [Show full text]
  • Synchrotron X-Ray Imaging of Pulmonary Alveoli in Respiration In
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE OPEN Synchrotron x-ray imaging of pulmonary SUBJECT AREAS: alveoli in respiration in live intact mice RESPIRATION Soeun Chang1,2*, Namseop Kwon1,3*, Jinkyung Kim1, Yoshiki Kohmura4, Tetsuya Ishikawa4, IMAGING TECHNIQUES Chin Kook Rhee5, Jung Ho Je1,2,4 & Akira Tsuda6 IMAGING 1X-ray Imaging Center, Pohang University of Science and Technology, San 31, Hyoja-dong, Pohang, 790-784, Korea, 2Department Received of Materials Science and Engineering, Pohang University of Science and Technology, San 31, Hyoja-dong, Pohang, 790-784, Korea, 3School of Interdisciplinary Bioscience and Bioengineering, Pohang University of Science and Technology, San 31, Hyoja- 19 September 2014 4 5 dong, Pohang, 790-784, Korea, RIKEN SPring-8 Center, 1-1-1 Kouto, Sayo-cho, Sayo, Hyogo, 679-5198, Japan, Division of Accepted Pulmonary and Critical Care Medicine, Department of Internal Medicine, Seoul St. Mary’s Hospital, Catholic University of Korea, 6 3 February 2015 505 Banpo-dong, Seocho-Gu, Seoul, 137-701, Korea, Harvard School of Public Health, Boston, Massachusetts, USA. Published 4 March 2015 Despite nearly a half century of studies, it has not been fully understood how pulmonary alveoli, the elementary gas exchange units in mammalian lungs, inflate and deflate during respiration. Understanding alveolar dynamics is crucial for treating patients with pulmonary diseases. In-vivo, real-time visualization of the alveoli during respiration has been hampered by active lung movement. Previous studies have been Correspondence and therefore limited to alveoli at lung apices or subpleural alveoli under open thorax conditions. Here we report requests for materials direct and real-time visualization of alveoli of live intact mice during respiration using tracking X-ray should be addressed to microscopy.
    [Show full text]
  • Regulation of Silica-Induced Pulmonary Inflammation
    University of Montana ScholarWorks at University of Montana Graduate Student Theses, Dissertations, & Professional Papers Graduate School 2014 Regulation of silica-induced pulmonary inflammation Rupa Biswas The University of Montana Follow this and additional works at: https://scholarworks.umt.edu/etd Let us know how access to this document benefits ou.y Recommended Citation Biswas, Rupa, "Regulation of silica-induced pulmonary inflammation" (2014). Graduate Student Theses, Dissertations, & Professional Papers. 4394. https://scholarworks.umt.edu/etd/4394 This Dissertation is brought to you for free and open access by the Graduate School at ScholarWorks at University of Montana. It has been accepted for inclusion in Graduate Student Theses, Dissertations, & Professional Papers by an authorized administrator of ScholarWorks at University of Montana. For more information, please contact [email protected]. Regulation of silica-induced pulmonary inflammation By Rupa Biswas At University of Montana Department of Biomedical and Pharmaceutical Sciences Center for Environmental Health Sciences Advisory Committee Members Andrij Holian, Ph.D., Chair Department of Biomedical and Pharmaceutical Sciences Kevan Roberts, Ph.D. Department of Biomedical and Pharmaceutical Sciences Howard Beall, Ph.D. Department of Biomedical and Pharmaceutical Sciences Christopher Migliaccio, Ph.D. Department of Biomedical and Pharmaceutical Sciences Stephen Lodmell, Ph.D. Division of Biological Sciences 1 Rupa Biswas Ph.D., June 2014 Toxicology Abstract Title: Regulation of silica-induced pulmonary inflammation Chairperson: Andrij Holian, Ph.D. Abstract Inhalation of crystalline silica for an extended period of time results in inflammation in the lungs, which plays a pivotal role in the development of silicosis, a progressive, inflammatory and fibrotic pulmonary disease. Inhaled silica particles are encountered by alveolar macrophages (AM) in the lungs.
    [Show full text]
  • 数字 Accessory Bronchus 副気管支 Accessory Fissure 副葉間裂
    数字 accentuation 亢進 accessory 副の 数字 accessory bronchus 副気管支 accessory fissure 副葉間裂 10-year survival 10年生存 accessory lobe 副肺葉 18F-fluorodeoxy glucose (FDG) 18F-フルオロデオキシグルコース accessory lung 副肺 2,3-diphosphoglycerate (2,3-DPG) 2,3ジフォスフォグリセレート accessory nasal sinus 副鼻腔 201TI (thallium-201) タリウム accessory trachea 副気管 5-fluorouracil(FU) 5-フルオロウラシル acclimation 順化 5-HT3 receptor antagonist 5-HT3レセプター拮抗薬 acclimation 馴化 5-hydroxytryptamine 5-ヒドロオキシトリプタミン acclimatization 気候順応 5-year survival 5年生存 acclimatization 順化 99mTc-macroaggregated albumin (99mTc-MAA) 99mTc標識大 acclimatization 馴化 凝集アルブミン accommodation 順応 accommodation 調節 accommodation to high altitude 高所順(適)応 A ACE polymorphism ACE遺伝子多型 acetone body アセトン体 abdomen 腹部 acetonuria アセトン尿[症] abdominal 腹部[側]の acetylcholine(ACh) アセチルコリン abdominal breathing 腹式呼吸 acetylcholine receptor (AchR, AChR) アセチルコリン受容体(レセプ abdominal cavity 腹腔 ター) abdominal pressure 腹腔内圧 acetylcholinesterase (AchE, AChE) アセチルコリンエステラーゼ abdominal respiration 腹式呼吸 achalasia アカラシア abdominal wall reflex 腹壁反射 achalasia 弛緩不能症 abduction 外転 achalasia [噴門]無弛緩[症] aberrant 走性 achromatocyte (achromocyte) 無血色素[赤]血球 aberrant 迷入性 achromatocyte (achromocyte) 無へモグロビン[赤]血球 aberrant artery 迷入動脈 acid 酸 aberration 迷入 acid 酸性 ablation 剥離 acid base equilibrium 酸塩基平衡 abnormal breath sound(s) 異常呼吸音 acid fast 抗酸性の abortive 早産の acid fast bacillus 抗酸菌 abortive 頓挫性(型) acid-base 酸―塩基 abortive 不全型 acid-base balance 酸塩基平衡 abortive pneumonia 頓挫[性]肺炎 acid-base disturbance 酸塩基平衡異常 abrasion 剥離 acid-base equilibrium 酸塩基平衡 abscess 膿瘍 acid-base regulation 酸塩基調節 absolute
    [Show full text]
  • Quantification of the Tissue Changes in the Human Lung with Chronic Lung Disease Using a Combination of Computed Tomography and Stereology
    QUANTIFICATION OF THE TISSUE CHANGES IN THE HUMAN LUNG WITH CHRONIC LUNG DISEASE USING A COMBINATION OF COMPUTED TOMOGRAPHY AND STEREOLOGY by HARVEY OWEN COXSON B.Sc, The University of British Columbia, 1986 A THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIRMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY in THE FACULTY OF GRADUATE STUDIES (Department of Experimental Medicine) We a^ept this thesis as>GOTTfl7rfning ;te>fhe required standard THE UNIVERSITY OF BRITISH COLUMBIA April 1998 © Harvey Owen Coxson, 1998 In presenting this thesis in partial fulfilment of the requirements for an advanced degree at the University of British Columbia, I agree that the Library shall make it freely available for reference and study. I further agree that permission for extensive copying of this thesis for scholarly purposes may be granted by the head of my department or by his or her representatives. It is understood that copying or publication of this thesis for financial gain shall not be allowed without my written permission. Department of The University of British Columbia Vancouver, Canada DE-6 (2/88) ABSTRACT Idiopathic pulmonary fibrosis (IPF) and pulmonary emphysema are chronic lung diseases exhibiting progressive deterioration in pulmonary function as the lung architecture is remodeled. This thesis quantifies these tissue changes using a novel combination of computed tomography (CT) and quantitative histology. Pre-operative CT scans were obtained from patients with IPF, patients receiving lung volume reduction surgery for diffuse emphysema and from patients with minimal to mild emphysema undergoing lobectomy for a small peripheral • •• • • • j. tumour. Total lung volume was calculated using the pixel dimensions on the CT scan while airspace and tissue volume as well as the regional lung expansion were estimated using the X- ray attenuation values.
    [Show full text]
  • Characterization of Air Flow and Lung Function in the Pulmonary Acinus by Fluid-Structure Interaction in Idiopathic Interstitial Pneumonias
    RESEARCH ARTICLE Characterization of air flow and lung function in the pulmonary acinus by fluid-structure interaction in idiopathic interstitial pneumonias 1 2 Long Chen , Xia ZhaoID * 1 College of Aerospace Engineering, Nanjing University of Aeronautics and Astronautics, Nanjing, Jiangsu, China, 2 Department of Rheumatology, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China * [email protected] a1111111111 a1111111111 a1111111111 Abstract a1111111111 a1111111111 Background and objective The idiopathic interstitial pneumonias (IIPs) are diffuse parenchymal lung disorders that are associated with substantial morbidity and mortality. Early diagnosis and disease stratifica- OPEN ACCESS tion of IIP patients are important because these are related with the treatment and progno- Citation: Chen L, Zhao X (2019) Characterization of sis. Idiopathic pulmonary fibrosis (IPF) and nonspecific interstitial pneumonia (NSIP) are air flow and lung function in the pulmonary acinus by fluid-structure interaction in idiopathic interstitial two major distinctive pathologic patterns of pulmonary fibrosis. We researched the applica- pneumonias. PLoS ONE 14(3): e0214441. https:// tion of the fluid-structure interaction (FSI) to the respiratory system and compared the pul- doi.org/10.1371/journal.pone.0214441 monary acinus mechanics and functions in healthy and IIP models. Editor: Josue Sznitman, Technion Israel Institute of Technology, ISRAEL Methods Received: October 26, 2018 The human pulmonary alveolus is idealized by a three-dimensional honeycomb-like geome- Accepted: March 13, 2019 try, and a fluid-structure interaction analysis is performed to study the normal and diseased Published: March 28, 2019 breathing mechanics. The computational domain consists of two generations of alveolar Copyright: © 2019 Chen, Zhao. This is an open ducts within the pulmonary acinus, with alveolar geometries approximated as closely access article distributed under the terms of the packed 14-sided polygons.
    [Show full text]
  • Type 2 Alveolar Cells Are Stem Cells in Adult Lung Christina E
    Research article Type 2 alveolar cells are stem cells in adult lung Christina E. Barkauskas,1 Michael J. Cronce,2 Craig R. Rackley,1 Emily J. Bowie,2 Douglas R. Keene,3 Barry R. Stripp,1 Scott H. Randell,4 Paul W. Noble,1 and Brigid L.M. Hogan2 1Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Duke University Medical Center, Durham, North Carolina, USA. 2Department of Cell Biology, Duke University, Durham, North Carolina, USA. 3Shriners Research Center, Portland, Oregon, USA. 4Department of Cell Biology and Physiology, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA. Gas exchange in the lung occurs within alveoli, air-filled sacs composed of type 2 and type 1 epithelial cells (AEC2s and AEC1s), capillaries, and various resident mesenchymal cells. Here, we use a combination of in vivo clonal lineage analysis, different injury/repair systems, and in vitro culture of purified cell populations to obtain new information about the contribution of AEC2s to alveolar maintenance and repair. Genetic lineage-tracing experiments showed that surfactant protein C–positive (SFTPC-positive) AEC2s self renew and differentiate over about a year, consistent with the population containing long-term alveolar stem cells. Moreover, if many AEC2s were specifically ablated, high-resolution imaging of intact lungs showed that individual survivors undergo rapid clonal expansion and daughter cell dispersal. Individual lineage-labeled AEC2s placed into 3D culture gave rise to self-renewing “alveolospheres,” which contained both AEC2s and cells expressing multiple AEC1 markers, including HOPX, a new marker for AEC1s. Growth and differentiation of the alveolospheres occurred most readily when cocultured with primary PDGFRα+ lung stromal cells.
    [Show full text]
  • Silicosis and Smoking: Intrinsic Phenomenon in the Respiratory System
    Advances in Applied Sociology, 2018, 8, 659-667 http://www.scirp.org/journal/aasoci ISSN Online: 2165-4336 ISSN Print: 2165-4328 Silicosis and Smoking: Intrinsic Phenomenon in the Respiratory System Diemen Delgado Garcia1*, Nayab Mahmood Sultan2, Oscar Ramirez Yerba3, Sofia Jimenez Castro4, Enmanuel Agila Palacios5, Ashley Delgado Cano1 1Research Institute for Safety and Health at Work, University of Guadalajara, Guadalajara, Mexico 2Department of Environmental Sciences and Earth, University of Birmingham, Birmingham, UK 3Occupational Medicine and the Environment, Scientific University of the South, Lima, Peru 4Occupational Medicine, University of Manchester, Manchester, UK 5Faculty of Security and Risks, University of the Armed Forces of Ecuador, Quito, Ecuador How to cite this paper: Garcia, D., Sultan, Abstract N. M., Yerba, O. R., Castro, S. J., Palacios, E. A., & Cano, A. D. (2018). Silicosis and Purpose of the Review: Some physiopathological mechanisms that could Smoking: Intrinsic Phenomenon in the support the relationship between tobacco and silicosis have been postulated Respiratory System. Advances in Applied but exact pathogenesis remains unknown. Recent Findings: Local inflamma- Sociology, 8, 659-667. https://doi.org/10.4236/aasoci.2018.810039 tion in workers with silicosis is a complex process characterized by an infil- tration of inflammatory cells in the respiratory alveolus, accompanied by an Received: July 31, 2018 increase in the expression of cytokines, chemokines, enzymes, growth factors Accepted: September 27, 2018 and adhesion molecules. Although in smokers without silicosis a similar pat- Published: September 30, 2018 tern of inflammation can be observed, in workers with silicosis this process Copyright © 2018 by authors and seems to be characterized by more pronounced increases in structural dam- Scientific Research Publishing Inc.
    [Show full text]