Activation of human T-lymphocytes. A kinetic and stereological study
- PMID: 316728
- DOI: 10.1007/BF00238051
Activation of human T-lymphocytes. A kinetic and stereological study
Abstract
Stereological data of phytohaemagglutinin (PHA)-activated human T-lymphocytes were recorded at intervals (12 to 72 h) together with biochemical (isotope-uptake, lymphotoxin-release) and morphological measurements. About 98% of the cells were activated 12 h after PHA-stimulation. The activation phase lasted less than 48 h, i.e., cells entering the activation phase within 12 h were at their activation maximum by 48 h. The activated cell increased in size. The nuclear/cytoplasmic-ratio decreased. Most of the cytoplasmic organelles developed in phase with the increase of cytoplasmic volume. After 48 h, mitotic figures were frequently seen. Due to the increasing number of secondary, activated daughter cells, parameters of most cytoplasmic components declined between 48 and 72 h. Structural changes in the nucleus preceded the 3H-leucine uptake, which had not reached its maximum after 72 h of incubation. The 3H-leucine uptake started as early as 12 h after culture initiation, and its increase was proportional to the increasing polyribosome density. No maximum uptake was reached up to 72 h, but the development of structural components related to this uptake was at its maximum at the end of the activation phase (48 h). The formation of bound ribosomes occurred subsequent to the enlargement of the surface of the rough endoplasmic reticulum. Initial polysome formation occurred at the expense of existing free ribosomes.
Similar articles
-
Carboxyfluorescein succinimidyl ester-based proliferative assays for assessment of T cell function in the diagnostic laboratory.Immunol Cell Biol. 1999 Dec;77(6):559-64. doi: 10.1046/j.1440-1711.1999.00870.x. Immunol Cell Biol. 1999. PMID: 10571678
-
Inhibition of phytohaemagglutinin-induced transformation of lymphocytes by human spleen extracts.Rev Esp Fisiol. 1981 Jun;37(2):159-64. Rev Esp Fisiol. 1981. PMID: 7313273
-
Antisense-mediated loss of calcium homoeostasis endoplasmic reticulum protein (CHERP; ERPROT213-21) impairs Ca2+ mobilization, nuclear factor of activated T-cells (NFAT) activation and cell proliferation in Jurkat T-lymphocytes.Biochem J. 2003 Jul 1;373(Pt 1):133-43. doi: 10.1042/BJ20030013. Biochem J. 2003. PMID: 12656674 Free PMC article.
-
Stereological model system for free cells and base-line data for human peripheral blood-derived small T-lymphocytes.Cell Tissue Res. 1978 Aug 25;192(1):121-42. doi: 10.1007/BF00231028. Cell Tissue Res. 1978. PMID: 308396
-
Lymphotoxin and chemotactic factor produced in vitro by human lymphocytes during their proliferative response in the presence of phytohaemagglutinin and Nocardia water-soluble mitogen.Ann Immunol (Paris). 1980 Sep-Oct;131D(2):223-32. Ann Immunol (Paris). 1980. PMID: 6970542
Cited by
-
Suppression of blastogenesis and proliferation of activated CD4(+) T cells: intravenous immunoglobulin (IVIg) versus novel anti-human leucocyte antigen (HLA)-E monoclonal antibodies mimicking HLA-I reactivity of IVIg.Clin Exp Immunol. 2014 Oct;178(1):154-77. doi: 10.1111/cei.12391. Clin Exp Immunol. 2014. PMID: 24889882 Free PMC article.
-
Ultrastructural morphometry of blastogenesis. II. Stimulated lymphocytes, the progeny of blast cells induced in vivo with DNCB.Cell Tissue Res. 1981;215(3):643-9. doi: 10.1007/BF00233538. Cell Tissue Res. 1981. PMID: 7214500
-
Paradoxical imbalance between activated lymphocyte protein synthesis capacity and rapid division rate.Elife. 2024 Mar 21;12:RP89015. doi: 10.7554/eLife.89015. Elife. 2024. PMID: 38512721 Free PMC article.
-
Nucleolar changes in human phytohaemagglutinin-stimulated lymphocytes.Cell Tissue Res. 1980;213(2):351-60. doi: 10.1007/BF00234793. Cell Tissue Res. 1980. PMID: 6161703
-
Calcium Dynamics of Ex Vivo Long-Term Cultured CD8+ T Cells Are Regulated by Changes in Redox Metabolism.PLoS One. 2016 Aug 15;11(8):e0159248. doi: 10.1371/journal.pone.0159248. eCollection 2016. PLoS One. 2016. PMID: 27526200 Free PMC article.