Advertisement
Research Article| Volume 81, ISSUE 1, P95-104, January 1973

Download started.

Ok

Connective tissue activation. V. The flux of connective tissue activating peptide during acute inflammation

  • C.William Castor
    Correspondence
    Reprint requests: Dr. C. William Castor, Department of Internal Medicine, Rackham Arthritis Research Unit, University of Michigan Medical Center, Ann Arbor, Mich. 48104.
    Affiliations
    From the Department of Internal Medicine and the Rackham Arthritis Research Unit, University of Michigan Medical Center, Ann Arbor, Mich. U.S.A.
    Search for articles by this author
      This paper is only available as a PDF. To read, Please Download here.

      Abstract

      The present experiments measured the amount of activator peptide present in an inflammatory granuloma during its evolution in vivo. Cotton pellets were implanted subcutaneously in male Sprague-Dawley rats, and the resulting inflammatory granulomas were harvested at intervals after implantation. The activator peptide concentration of cotton pellet granulomas (units per 100 μg DNA) was elevated at day 4, reached a peak at day 7, and returned to very low levels by 14 days. The hyaluronic acid (HA) concentration of the granuloma was also greatest on day 7, while the concentration of sulfated MPS tended to be highest by 14 days. The molecular weight (intrinsic viscosity) of hyaluronate in the early granuloma was significantly greater than that found at 14 days and later. Collagen was present in high concentration by 7 days. At 4 days polymorphonuclear leukocytes were a major portion of the cell population, but by 7 days the dominant cell types were fibrocytes and foreign-body giant cells. The elevated level of connective tissue activating peptide (CTAP) found early in the inflammatory process is in keeping with its postulated role as a regulator of the transition from the exudative phase of inflammation to the reparative phase. The concomitant peak concentration of HA in the granuloma is in agreement with the known in vitro actions of connective tissue activating peptide.
      To read this article in full you will need to make a payment

      Purchase one-time access:

      Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online access
      One-time access price info
      • For academic or personal research use, select 'Academic and Personal'
      • For corporate R&D use, select 'Corporate R&D Professionals'

      Subscribe:

      Subscribe to Translational Research
      Already a print subscriber? Claim online access
      Already an online subscriber? Sign in
      Institutional Access: Sign in to ScienceDirect

      References

        • Yaron M
        • Castor CW
        Leukocyte-connective tissue cell interaction. I. Stimulation of hyaluronate synthesis by live and dead leukocytes.
        Arthritis Rheum. 1969; 12: 365-373
        • Castor CW
        • Yaron M
        Leukocyte-connective tissue cell interaction. II. The specificity, duration, and mechanism of interaction effects.
        Arthritis Rheum. 1969; 12: 374-386
        • Castor CW
        • Dorstewitz EL
        • Smith SF
        • et al.
        Connective tissue activation. I. The nature, specificity, measurement, and distribution of connective tissue activating peptide.
        Arthritis Rheum. 1971; 14: 41-54
        • Castor CW
        • Smith SF
        • Ritchie JC
        • et al.
        Connective tissue activation. II. Abnormalities of cultured rheumatoid synovial cells.
        Arthritis Rheum. 1971; 14: 55-66
        • Castor CW
        Connective tissue activation. III. Observations on the mechanism of action of connective tissue activating peptide.
        J Lab Clin Med. 1972; 79: 285-301
        • Winder CV
        • Wax J
        • Scotti L
        • et al.
        Anti-inflammatory, antipyretic, and antinociceptive properties of N- (2, 3-sylyl) anthranilic acid (mefenamic acid).
        J Pharmacol Exp Ther. 1962; 138: 405-413
        • Castor CW
        • Prince RK
        • Dorstewitz EL
        Characteristics of human “fibroblasts” cultivated from different anatomical sites.
        Lab Invest. 1962; 11: 703-713
        • Castor CW
        • Dorstewitz EL
        Abnormalities of connective tissue cells cultured from patients with rheumatoid arthritis. I. Relative unresponsiveness of rheumatoid articular cells to hydrocortisone.
        J lab clin med. 1966; 68: 300-313
        • Castor CW
        • Dorstewitz EL
        • Rowe K
        • et al.
        Abnormalities of connective tissue cells cultured from patients with rheumatoid arthritis. II. Defective regulation of hyaluronate and collagen formation.
        J Lab Clin Med. 1971; 77: 65-75
        • Bitter T
        • Muir HM
        A modified uronic acid carbazole reaction.
        Anal Biochem. 1962; 4: 330-334
        • Castor CW
        • Wright D
        • Buckingham RB
        Effects of rheumatoid sera on fibroblast proliferation and hyaluronic acid synthesis.
        Arthritis Rheum. 1968; 11: 652-659
        • Gibson QH
        • Swoboda BEP
        • Massey V
        Kinetics and mechanism of action of glucose oxidase.
        J Biol Chem. 1964; 239: 3927-3934
        • Barker SB
        • Summerson WH
        The colorimetric determination of lactic acid in biological material.
        J Biol Chem. 1941; 138: 535-554
        • Oyama VI
        • Eagle H
        Measurement of cell growth in tissue culture with a phenol reagent (Folin-Cioealteau).
        in: Ed. 4. Proc Soc Exp Biol Med. 91. 1956: 305-307
        • Burton K
        A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of desoxyribonucleic acid.
        J Biol Chem. 1956; 62: 315-323
        • Korn ED
        Purines and pyrimidines.
        in: Colwick SP Kaplan ND Methods in Enzymology IV. Academic Press, New York1957: 632-634
        • Woessner Jr, JF
        The determination of hydroxyproline in tissue and protein samples containing small proportions of this imino acid.
        Arch Biochem. 1961; 93: 440-447
        • Heyworth R
        • Perkins HR
        • Walter PG
        Paper chromatography of hexosamiues and N-acetylhexosamines.
        Nature. 1961; 190: 261-262
        • Moffat ED
        • Lytle RI
        Polychromatic technique for the identification of amino acids on paper chromatograms.
        Anal Chem. 1959; 31: 926-928
        • Roseman S
        • Daffner I
        Colorimetric method for determination of glucosamine and galactosamine.
        Anal Chem. 1956; 28: 1743-1746
        • Castor CW
        • Dorstewitz EL
        Identification of acid mucopolysaccharides by paper chromatography.
        J Chromatogr. 1964; 13: 157-165
      1. Castor CW: Unpublished observations.