PMID- 8182229 OWN - NLM STAT- MEDLINE DCOM- 19940616 LR - 20220331 IS - 0091-6749 (Print) IS - 0091-6749 (Linking) VI - 93 IP - 5 DP - 1994 May TI - Expression of transforming growth factors-alpha and beta 1 messenger RNA and product by eosinophils in nasal polyps. PG - 864-9 AB - Nasal polyps are thought to develop as a manifestation of a chronic inflammatory process involving the upper airways. The eosinophil characteristically represents a prominent component of the inflammatory cell infiltrate of these lesions. However, the major clinical problem associated with nasal polyps, nasal obstruction, reflects the proliferation of the stromal and epithelial elements, which constitute the bulk of these lesions. We recently reported that blood eosinophils of patients with hypereosinophilia can produce the cytokines transforming growth factors-alpha (TGF-alpha) and beta 1 (TGF-beta 1). These cytokines have many biologic activities, which include the regulation of epithelial proliferation, the promotion of extracellular matrix formation, and the induction of angiogenesis. We therefore used in situ hybridization to determine whether the eosinophils that infiltrate nasal polyps express TGF-alpha and/or TGF-beta 1 messenger RNA and used immunohistochemistry to determine whether these eosinophils also express TGF-alpha and TGF-beta 1 proteins. We found that eosinophils represented a major source of both transforming growth factors in each case of nasal polyposis examined and that in most cases the majority of all eosinophils expressed both TGF-alpha and TGF-beta 1. These results suggest that production of TGF-alpha and TGF-beta 1 by the infiltrating eosinophils may contribute to some of the pathologic changes observed in nasal polyposis, such as thickening of the epithelial basement membrane, stromal fibrosis, angiogenesis, and epithelial and glandular hyperplasia. FAU - Elovic, A AU - Elovic A AD - Department of Oral Medicine and Diagnostic Sciences, Harvard School of Dental Medicine, Boston, MA 02115. FAU - Wong, D T AU - Wong DT FAU - Weller, P F AU - Weller PF FAU - Matossian, K AU - Matossian K FAU - Galli, S J AU - Galli SJ LA - eng GR - AI-22674/AI/NIAID NIH HHS/United States GR - DE-08680/DE/NIDCR NIH HHS/United States GR - DE-10335/DE/NIDCR NIH HHS/United States GR - etc. PT - Journal Article PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - J Allergy Clin Immunol JT - The Journal of allergy and clinical immunology JID - 1275002 RN - 0 (Aniline Compounds) RN - 0 (Fluorescent Dyes) RN - 0 (Proteins) RN - 0 (RNA, Messenger) RN - 0 (Rhodamines) RN - 0 (Transforming Growth Factor alpha) RN - 0 (Transforming Growth Factor beta) RN - 8004-91-9 (aniline blue) SB - IM MH - *Aniline Compounds MH - Eosinophils/*metabolism MH - Fluorescence MH - Fluorescent Dyes MH - Humans MH - Immunohistochemistry MH - In Situ Hybridization MH - Nasal Polyps/*metabolism MH - Proteins/*metabolism MH - RNA, Messenger/*metabolism MH - Rhodamines MH - Transforming Growth Factor alpha/*metabolism MH - Transforming Growth Factor beta/*metabolism EDAT- 1994/05/01 00:00 MHDA- 1994/05/01 00:01 CRDT- 1994/05/01 00:00 PHST- 1994/05/01 00:00 [pubmed] PHST- 1994/05/01 00:01 [medline] PHST- 1994/05/01 00:00 [entrez] AID - 0091-6749(94)90379-4 [pii] AID - 10.1016/0091-6749(94)90379-4 [doi] PST - ppublish SO - J Allergy Clin Immunol. 1994 May;93(5):864-9. doi: 10.1016/0091-6749(94)90379-4.