Alveolar macrophage cell line is not activated by exposure to polymeric microspheres

被引:13
作者
Ng, K
Stringer, KA
Cohen, Z
Serravo, R
Tian, B
Meyer, JD
Falk, R
Randolph, T
Manning, MC
Thompson, DC
机构
[1] Univ Colorado, Hlth Sci Ctr, Sch Pharm, Dept Pharmaceut Sci, Denver, CO 80262 USA
[2] Univ Colorado, Hlth Sci Ctr, Sch Pharm, Dept Pharm Practice, Denver, CO 80262 USA
[3] Univ Colorado, Dept Chem Engn, Boulder, CO 80309 USA
关键词
alveolar macrophage; NR8383; endocytosis; poly(L-lactide) microsphere; precipitation with compressed anti-solvent; oxidative burst and TNF-alpha;
D O I
10.1016/S0378-5173(98)00138-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
An in vitro cell culture model based on a rat alveolar macrophage (AM) cell line, NR8383, was used to determine if poly(L-lactide) (PLA) microspheres prepared by the precipitation with a compressed antisolvent (PCA) method can be taken up by AMs and activate AMs. To examine cellular uptake of microspheres, microspheres were labeled with rhodamine 6G. Using fluorescence microscopy, the uptake of microspheres by NR8383 cells was followed as a function of time, microsphere concentration, and susceptibility to lysosomotropic agents. To determine if microspheres can activate NR8383 cells, the oxidative burst and production of TNF-alpha by NRS383 cells following microsphere treatment was measured. Uptake of microspheres by NRS383 cells was dependent on microsphere concentration and appeared to occur via endocytosis, as uptake was significantly inhibited by the putative lysosomotropic agents, ammonium chloride and chloroquine. Furthermore, the microspheres do not appear to activate NR8383 cells, since microsphere exposure results in negligible oxidative burst and TNF-alpha production in NR8383. Microspheres prepared by the PCA method hold great potential in targeting drugs to AMs and, therefore, may be of utility for the treatment of diseases in which AMs play an important role, such as tuberculosis (TB). (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:41 / 49
页数:9
相关论文
共 21 条
[1]  
[Anonymous], USE ANTIBIOTICS
[2]   DETECTION OF ACTIVATED O-2 SPECIES INVITRO AND IN RAT LUNGS BY CHEMI-LUMINESCENCE [J].
ARCHER, SL ;
NELSON, DP ;
WEIR, EK .
JOURNAL OF APPLIED PHYSIOLOGY, 1989, 67 (05) :1912-1921
[3]  
BASS J, 1992, AM REV RESPIR DIS, V146, P1623
[4]  
BASS JB, 1990, AM REV RESPIR DIS, V142, P725
[5]  
Centers for Disease Control (CDC), 1989, MMWR Suppl, V38, P1
[6]   DELAYED-TYPE HYPERSENSITIVITY AND CELL-MEDIATED-IMMUNITY IN THE PATHOGENESIS OF TUBERCULOSIS [J].
DANNENBERG, AM .
IMMUNOLOGY TODAY, 1991, 12 (07) :228-233
[7]   CYTOKINE AND GROWTH-FACTOR RELEASE BY ALVEOLAR MACROPHAGES - POTENTIAL BIOMARKERS OF PULMONARY TOXICITY [J].
DRISCOLL, KE ;
MAURER, JK .
TOXICOLOGIC PATHOLOGY, 1991, 19 (04) :398-405
[8]   Controlled release of ionic compounds from poly (L-lactide) microspheres produced by precipitation with a compressed antisolvent [J].
Falk, R ;
Randolph, TW ;
Meyer, JD ;
Kelly, RM ;
Manning, MC .
JOURNAL OF CONTROLLED RELEASE, 1997, 44 (01) :77-85
[9]  
FANTONE JC, 1982, AM J PATHOL, V107, P397
[10]  
HELMKE RJ, 1987, IN VITRO CELL DEV B, V23, P567