Literature DB >> 19868996

THE RELATIVE REACTION WITHIN LIVING MAMMALIAN-TISSUES : II. ON THE MOBILIZATION OF ACID MATERIAL WITHIN CELLS, AND THE REACTION AS INFLUENCED BY THE CELL STATE.

P Rous1.   

Abstract

The acidity of the macrophage granules in which litmus comes to be stored during life is considerable. It has proved possible to stain these granules in vivo with some of the phthalein indicators and the results, had they been obtained under controlled conditions, would indicate a pH of 3.0 or less. The amount of acid material which may accumulate within the cells of animals stained with litmus is great, sufficient in the case of the elements of a peritoneal exudate for the acid reaction to prevail when they are gathered together and crushed. The material is derived, not from the dye, but from living elements responding characteristically to a stimulus far from unique. Such responses may well play a rôle in normal physiological activities and in the cellular defense against microorganisms. Vital staining with litmus demonstrates anew that the intracellular reaction during life is independent of that of the body fluids. By means of color changes in the stored indicator one can distinguish sick as well as dead cells of certain sorts and follow their distribution and fate within the organism. There are data to suggest that with the aid of the indicator the normal period of survival of certain elements at least can be determined. By the indicator method, of which the foregoing observations afford a crude illustration, much should be learnt in the future about body processes. The present paper is the second of a series upon the theme.

Entities:  

Year:  1925        PMID: 19868996      PMCID: PMC2130947          DOI: 10.1084/jem.41.3.399

Source DB:  PubMed          Journal:  J Exp Med        ISSN: 0022-1007            Impact factor:   14.307


  1 in total

1.  THE PROTECTION OF PATHOGENIC MICROORGANISMS BY LIVING TISSUE CELLS.

Authors:  P Rous; F S Jones
Journal:  J Exp Med       Date:  1916-05-01       Impact factor: 14.307

  1 in total
  22 in total

1.  Cellular death and necrosis: chemical, physical and morphologic changes in rat liver.

Authors:  G MAJNO; M LA GATTUTA; T E THOMPSON
Journal:  Virchows Arch Pathol Anat Physiol Klin Med       Date:  1960

Review 2.  Acid resistance in Mycobacterium tuberculosis.

Authors:  Omar H Vandal; Carl F Nathan; Sabine Ehrt
Journal:  J Bacteriol       Date:  2009-05-22       Impact factor: 3.490

3.  [Specificity of calcium determination using tetracycline].

Authors:  J Winckler; W Westphal
Journal:  Histochemie       Date:  1973

Review 4.  [Intracellular proteolysis].

Authors:  P Bohley
Journal:  Naturwissenschaften       Date:  1968-05

5.  The influence of the biochemical milieu on the development of tubercles in the testis and epididymis.

Authors:  D Engel
Journal:  Beitr Klin Erforsch Tuberk Lungenkr       Date:  1968

6.  Enzymes as Factors in Resistance to Tuberculosis: IV. Effect of Liver Enzymes on Tubercle Phosphatide.

Authors:  B Gerstl; R Tennant; O Pelzman
Journal:  Yale J Biol Med       Date:  1945-01

7.  The role of mycobacteria and the effect of proteolytic degradation of thyroglobulin on the production of autoimmune thyroiditis.

Authors:  W O Weigle; G J High; R M Nakamura
Journal:  J Exp Med       Date:  1969-08-01       Impact factor: 14.307

8.  Characterization of leukin: an antibacterial factor from leucocytes active against gram-positive pathogens.

Authors:  R C SKARNES; D W WATSON
Journal:  J Exp Med       Date:  1956-12-01       Impact factor: 14.307

Review 9.  Cell-autonomous effector mechanisms against mycobacterium tuberculosis.

Authors:  John D MacMicking
Journal:  Cold Spring Harb Perspect Med       Date:  2014-07-31       Impact factor: 6.915

10.  Characterization of murine macrophages from bone marrow, spleen and peritoneum.

Authors:  Changqi Wang; Xiao Yu; Qi Cao; Ya Wang; Guoping Zheng; Thian Kui Tan; Hong Zhao; Ye Zhao; Yiping Wang; David Ch Harris
Journal:  BMC Immunol       Date:  2013-02-05       Impact factor: 3.615

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.