Abstract
A new in vitro model has been developed for studying migration of human polymorphonuclear leukocytes (PMN) through living native cellular and matrix barriers. Human amnion membrane consists of a single layer of epithelium bound to a continuous basement membrane interfacing an avascular collagenous stroma. Living amnion was placed in plastic chambers with separate compartments on each side of the membrane. PMN were introduced on the epithelial side of the amnion, and a Millipore filter (Millipore Corp., Bedford, Mass.) was placed against the stromal side. In response to N-formylmethionyl-leucyl- phenylanlanine (FMLP) chemoattractant, PMN penetrated the full thickness of the amnion and were collected and counted on the filter. The rate of PMN traversal of the amnion was dependent on the concentration of FMLP (optimal at 10(-8)M) as well as the slope of the FMLP gradient across the amnion. The route of PMN migration was studied by transmission electron microscopy. PMN first attached to the epithelial surface, then infiltrated between intercellular junctions. PMN migrated around or through tight junction and hemidesmosome attachments. The PMN then penetrated the basement membrane and migrated through the dense collagenous stroma. The present amnion migration system has characteristics of the in vivo inflammatory state not described in any previous method for monitoring PMN migration in vitro. Prior methods have not used native epithelium, whole basement membrane, or collagenous stroma. PMN penetration of these barriers occurs in the normal inflammatory response and probably involves biochemical mechanisms not required for simple migration through the pores of an artificial filter. The amnion system can be useful for future biochemical and morphological studies of PMN penetration of these barriers and possible repair processes that may follow.
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Selected References
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- Anderson A. O., Anderson N. D. Lymphocyte emigration from high endothelial venules in rat lymph nodes. Immunology. 1976 Nov;31(5):731–748. [PMC free article] [PubMed] [Google Scholar]
- BOYDEN S. The chemotactic effect of mixtures of antibody and antigen on polymorphonuclear leucocytes. J Exp Med. 1962 Mar 1;115:453–466. doi: 10.1084/jem.115.3.453. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Becker E. L. Some interrelations of neutrophil chemotaxis, lysosomal enzyme secretion, and phagocytosis as revealed by synthetic peptides. Am J Pathol. 1976 Nov;85(2):385–394. [PMC free article] [PubMed] [Google Scholar]
- Cramer E. B., Gallin J. I. Localization of submembranous cations to the leading end of human neutrophils during chemotaxis. J Cell Biol. 1979 Aug;82(2):369–379. doi: 10.1083/jcb.82.2.369. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cramer E. B., Milks L. C., Ojakian G. K. Transepithelial migration of human neutrophils: an in vitro model system. Proc Natl Acad Sci U S A. 1980 Jul;77(7):4069–4073. doi: 10.1073/pnas.77.7.4069. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fehr J., Dahinden C. Modulating influence of chemotactic factor-induced cell adhesiveness on granulocyte function. J Clin Invest. 1979 Jul;64(1):8–16. doi: 10.1172/JCI109466. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gallin J. I., Clark R. A., Kimball H. R. Granulocyte chemotaxis: an improved in vitro assay employing 51 Cr-labeled granulocytes. J Immunol. 1973 Jan;110(1):233–240. [PubMed] [Google Scholar]
- Gallin J. I., Wright D. G., Schiffmann E. Role of secretory events in modulating human neutrophil chemotaxis. J Clin Invest. 1978 Dec;62(6):1364–1374. doi: 10.1172/JCI109257. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hoover R. L., Briggs R. T., Karnovsky M. J. The adhesive interaction between polymorphonuclear leukocytes and endothelial cells in vitro. Cell. 1978 Jun;14(2):423–428. doi: 10.1016/0092-8674(78)90127-7. [DOI] [PubMed] [Google Scholar]
- Kawaoka E. J., Miller M. E., Cheung A. T. Chemotactic factor-induced effects upon deformability of human polymorphonuclear leukocytes. J Clin Immunol. 1981 Jan;1(1):41–44. doi: 10.1007/BF00915475. [DOI] [PubMed] [Google Scholar]
- Keller H. U., Borel J. F., Wilkinson P. C., Hess M. W., Cottier H. Re-assessment of Boyden's technique for measuring chemotaxis. J Immunol Methods. 1972 Jan;1(2):165–168. doi: 10.1016/0022-1759(72)90043-9. [DOI] [PubMed] [Google Scholar]
- King B. F. A cytological study of plasma membrane modifications, intercellular junctions, and endocytic activity of amniotic epithelium. Anat Rec. 1978 Jan;190(1):113–125. doi: 10.1002/ar.1091900110. [DOI] [PubMed] [Google Scholar]
- Liotta L. A., Lee C. W., Morakis D. J. New method for preparing large surfaces of intact human basement membrane for tumor invasion studies. Cancer Lett. 1980 Dec;11(2):141–152. doi: 10.1016/0304-3835(80)90105-6. [DOI] [PubMed] [Google Scholar]
- Liotta L. A., Tryggvason K., Garbisa S., Hart I., Foltz C. M., Shafie S. Metastatic potential correlates with enzymatic degradation of basement membrane collagen. Nature. 1980 Mar 6;284(5751):67–68. doi: 10.1038/284067a0. [DOI] [PubMed] [Google Scholar]
- MARCHESI V. T., FLOREY H. W. Electron micrographic observations on the emigration of leucocytes. Q J Exp Physiol Cogn Med Sci. 1960 Oct;45:343–348. doi: 10.1113/expphysiol.1960.sp001489. [DOI] [PubMed] [Google Scholar]
- MARCHESI V. T. The site of leucocyte emigration during inflammation. Q J Exp Physiol Cogn Med Sci. 1961 Apr;46:115–118. doi: 10.1113/expphysiol.1961.sp001522. [DOI] [PubMed] [Google Scholar]
- Mainardi C. L., Dixit S. N., Kang A. H. Degradation of type IV (basement membrane) collagen by a proteinase isolated from human polymorphonuclear leukocyte granules. J Biol Chem. 1980 Jun 10;255(11):5435–5441. [PubMed] [Google Scholar]
- Marchesi V. T. Ultrastructural aspects of acute inflammation. Pathol Annu. 1970;5:343–353. [PubMed] [Google Scholar]
- Niedel J. E., Cuatrecasas P. Formyl peptide chemotactic receptors of leukocytes and macrophages. Curr Top Cell Regul. 1980;17:137–170. doi: 10.1016/b978-0-12-152817-1.50009-2. [DOI] [PubMed] [Google Scholar]
- O'Flaherty J. T., Kreutzer D. L., Ward P. A. Chemotactic factor influences on the aggregation, swelling, and foreign surface adhesiveness of human leukocytes. Am J Pathol. 1978 Mar;90(3):537–550. [PMC free article] [PubMed] [Google Scholar]
- O'Flaherty J. T., Kreutzer D. L., Ward P. A. Neutrophil aggregation and swelling induced by chemotactic agents. J Immunol. 1977 Jul;119(1):232–239. [PubMed] [Google Scholar]
- O'Flaherty J. T., Showell H. J., Becker E. L., Ward P. A. Substances which aggregate neutrophils. Mechanism of action. Am J Pathol. 1978 Jul;92(1):155–166. [PMC free article] [PubMed] [Google Scholar]
- O'Flaherty J. T., Ward P. A. Leukocyte aggregation induced by chemotactic factors: a review. Inflammation. 1978 Jun;3(2):177–194. doi: 10.1007/BF00910738. [DOI] [PubMed] [Google Scholar]
- Phillips D. M., Mahler S. Leukocyte emigration and migration in the vagina following mating in the rabbit. Anat Rec. 1977 Sep;189(1):45–59. doi: 10.1002/ar.1091890104. [DOI] [PubMed] [Google Scholar]
- Seelig L. L., Jr, Beer A. E. Transepithelial migration of leukocytes in the mammary gland of lactating rats. Biol Reprod. 1978 Jun;18(5):736–744. doi: 10.1095/biolreprod18.5.736. [DOI] [PubMed] [Google Scholar]
- Shaw J. O. Leukocytes in chemotactic-fragment-induced lung inflammation. Vascular emigration and alveolar surface migration. Am J Pathol. 1980 Nov;101(2):283–302. [PMC free article] [PubMed] [Google Scholar]
- Showell H. J., Freer R. J., Zigmond S. H., Schiffmann E., Aswanikumar S., Corcoran B., Becker E. L. The structure-activity relations of synthetic peptides as chemotactic factors and inducers of lysosomal secretion for neutrophils. J Exp Med. 1976 May 1;143(5):1154–1169. doi: 10.1084/jem.143.5.1154. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smith C. W., Hollers J. C., Patrick R. A., Hassett C. Motility and adhesiveness in human neutrophils. Effects of chemotactic factors. J Clin Invest. 1979 Feb;63(2):221–229. doi: 10.1172/JCI109293. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Spilberg I., Mehta J. Demonstration of a specific neutrophil receptor for a cell-derived chemotactic factor. J Clin Invest. 1979 Jan;63(1):85–88. doi: 10.1172/JCI109282. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Taylor R. F., Price T. H., Schwartz S. M., Dale D. C. Neutrophil-endothelial cell interactions on endothelial monolayers grown on micropore filters. J Clin Invest. 1981 Feb;67(2):584–587. doi: 10.1172/JCI110071. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Williams L. T., Snyderman R., Pike M. C., Lefkowitz R. J. Specific receptor sites for chemotactic peptides on human polymorphonuclear leukocytes. Proc Natl Acad Sci U S A. 1977 Mar;74(3):1204–1208. doi: 10.1073/pnas.74.3.1204. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zigmond S. H. Ability of polymorphonuclear leukocytes to orient in gradients of chemotactic factors. J Cell Biol. 1977 Nov;75(2 Pt 1):606–616. doi: 10.1083/jcb.75.2.606. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zigmond S. H. Chemotaxis by polymorphonuclear leukocytes. J Cell Biol. 1978 May;77(2):269–287. doi: 10.1083/jcb.77.2.269. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zigmond S. H., Sullivan S. J. Sensory adaptation of leukocytes to chemotactic peptides. J Cell Biol. 1979 Aug;82(2):517–527. doi: 10.1083/jcb.82.2.517. [DOI] [PMC free article] [PubMed] [Google Scholar]
- van Herendael B. J., Oberti C., Brosens I. Microanatomy of the human amniotic membranes. A light microscopic, transmission, and scanning electron microscopic study. Am J Obstet Gynecol. 1978 Aug 15;131(8):872–880. doi: 10.1016/s0002-9378(16)33135-0. [DOI] [PubMed] [Google Scholar]