PT  - JOURNAL ARTICLE
AU  - J J Powell
AU  - C C Ainley
AU  - R S Harvey
AU  - I M Mason
AU  - M D Kendall
AU  - E A Sankey
AU  - A P Dhillon
AU  - R P Thompson
TI  - Characterisation of inorganic microparticles in pigment cells of human gut associated lymphoid tissue.
AID  - 10.1136/gut.38.3.390
DP  - 1996 Mar 01
TA  - Gut
PG  - 390--395
VI  - 38
IP  - 3
4099  - http://gut.bmj.com/content/38/3/390.short
4100  - http://gut.bmj.com/content/38/3/390.full
SO  - Gut1996 Mar 01; 38
AB  - Macrophages at the base of human gut associated lymphoid tissue (GALT), become loaded early in life with dark granular pigment that is rich in aluminium, silicon, and titanium. The molecular characteristics, intracellular distribution, and source of this pigment is described. Laser scanning and electron microscopy showed that pigmented macrophages were often closely related to collagen fibres and plasma cells in GALT of both small and large intestine and contained numerous phagolysosomes, previously described as granules, that are rich in electron dense submicron sized particles. Morphological assessment, x ray microanalysis, and image electron energy loss spectroscopy showed three distinct types of microparticle: type I - spheres of titanium dioxide, 100-200 nm diameter, characterised as the synthetic food-additive polymorph anatase; type II - aluminosilicates, < 100-400 nm in length, generally of flaky appearance, often with adsorbed surface iron, and mostly characteristic of the natural clay mineral kaolinite; and type III - mixed environmental silicates without aluminium, 100-700 nm in length and of variable morphology. Thus, this cellular pigment that is partly derived from food additives and partly from the environment is composed of inert inorganic microparticles and loaded into phagolysosomes of macrophages within the GALT of all human subjects. These observations suggest that the pathogenicity of this pigment should be further investigated since, in susceptible individuals, the same intracellular distribution of these three types of submicron particle causes chronic latent granulomatous inflammation.