Literature DB >> 7896596

Quantitation of neutrophil migration in acute bacterial pneumonia in rabbits.

C M Doerschuk1, J Markos, H O Coxson, D English, J C Hogg.   

Abstract

The circulating neutrophils must slow down, adhere to the vessel walls, and migrate out of the microvasculature into the tissue and air spaces to defend the lung against microorganisms. The present study was designed to provide quantitative information about each of these steps. Streptococcus pneumoniae was instilled into the left lower lobe of New Zealand White rabbits to induce a pneumonia, and this lobe was compared with the same region of the opposite lung. The distribution of blood flow was determined by using radiolabeled macroaggregated albumin, and the patterns of perfusion within the capillary bed were quantitated using Monastral blue. The number of neutrophils delivered to the pneumonic site was determined by multiplying the circulating neutrophil count and blood flow. The results show that retention of 51Cr-labeled neutrophils was increased in the pneumonic region 2, 4, and 8 h after instillation of the organisms. The number of intracapillary neutrophils was increased in the pneumonic regions at all time points and in the control regions at 1 and 4 h. Neutrophil migration occurred in the pneumonic site, but only 1-2% of the total neutrophils delivered to the region migrated out of the pulmonary vessels into the air space. We conclude that the circulating neutrophils undergo a generalized response that increases their margination throughout the lung, that increased margination in the pneumonic site changes the distribution of capillary flow, and that the majority of neutrophils delivered to a pneumonic site are returned to the circulation without migrating into the air space.

Entities:  

Mesh:

Year:  1994        PMID: 7896596     DOI: 10.1152/jappl.1994.77.6.2593

Source DB:  PubMed          Journal:  J Appl Physiol (1985)        ISSN: 0161-7567


  15 in total

Review 1.  Streptococcus pneumoniae.

Authors:  J R Catterall
Journal:  Thorax       Date:  1999-10       Impact factor: 9.139

Review 2.  Chronic obstructive pulmonary disease - part 2: pathology and biochemistry of emphysema.

Authors:  J C Hogg; R M Senior
Journal:  Thorax       Date:  2002-09       Impact factor: 9.139

3.  Cytosolic Phospholipase A2α Promotes Pulmonary Inflammation and Systemic Disease during Streptococcus pneumoniae Infection.

Authors:  Rudra Bhowmick; Stacie Clark; Joseph V Bonventre; John M Leong; Beth A McCormick
Journal:  Infect Immun       Date:  2017-10-18       Impact factor: 3.441

Review 4.  Polymorphonuclear leucocyte traffic in lung inflammation.

Authors:  J C Hogg; B A Walker
Journal:  Thorax       Date:  1995-08       Impact factor: 9.139

5.  Regulation of systemic and local neutrophil responses by G-CSF during pulmonary Pseudomonas aeruginosa infection.

Authors:  Alyssa D Gregory; Lisa A Hogue; Thomas W Ferkol; Daniel C Link
Journal:  Blood       Date:  2006-12-21       Impact factor: 22.113

6.  Neutrophil margination, sequestration, and emigration in the lungs of L-selectin-deficient mice.

Authors:  N A Doyle; S D Bhagwan; B B Meek; G J Kutkoski; D A Steeber; T F Tedder; C M Doerschuk
Journal:  J Clin Invest       Date:  1997-02-01       Impact factor: 14.808

7.  Role of CD 11/CD 18 in neutrophil emigration during acute and recurrent Pseudomonas aeruginosa-induced pneumonia in rabbits.

Authors:  T Kumasaka; N A Doyle; W M Quinlan; L Graham; C M Doerschuk
Journal:  Am J Pathol       Date:  1996-04       Impact factor: 4.307

Review 8.  Homeostatic regulation of blood neutrophil counts.

Authors:  Sibylle von Vietinghoff; Klaus Ley
Journal:  J Immunol       Date:  2008-10-15       Impact factor: 5.422

9.  P-selectin/ICAM-1 double mutant mice: acute emigration of neutrophils into the peritoneum is completely absent but is normal into pulmonary alveoli.

Authors:  D C Bullard; L Qin; I Lorenzo; W M Quinlin; N A Doyle; R Bosse; D Vestweber; C M Doerschuk; A L Beaudet
Journal:  J Clin Invest       Date:  1995-04       Impact factor: 14.808

10.  Systemic disease during Streptococcus pneumoniae acute lung infection requires 12-lipoxygenase-dependent inflammation.

Authors:  Beth A McCormick; John M Leong; Rudra Bhowmick; Nang Maung; Bryan P Hurley; Elsa Bou Ghanem; Karsten Gronert
Journal:  J Immunol       Date:  2013-10-02       Impact factor: 5.422

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