ABSTRACT
BACKGROUND: Obesity is currently viewed as a state of chronic low-grade inflammation in which there is a pro-inflammatory alteration in the serum adipocytokine profile as well as an infiltration of white adipose tissue by activated macrophages. The etiology of this inflammation, however, is poorly understood. METHODS: Hypothesizing that local hypoxia within expanding white adipose tissue depots may contribute to obesity-related inflammation, we compared body composition, serum inflammatory marker concentrations and the expression of several hypoxia-regulated genes in white adipose tissue derived from lean, dietary-induced obese (DIO) and ob/ob male C57BL/6J mice. We also examined white adipose tissue for the presence of hypoxia using both a pimonidazole-based antibody system and a fiberoptic sensor for real-time pO(2) quantification in vivo. Finally, using cell-specific leukocyte antibodies, we performed immunohistochemistry and flow cytometric analyses to further characterize the cellular nature of adipose inflammation. RESULTS: We determined that obesity in male C57BL/6J mice is associated with increased expression of HIF (hypoxia-inducible factor) isoforms and GLUT-1, and that white adipose tissue hypoxia was present in the obese mice. Immunohistochemistry revealed hypoxic areas to colocalize predominantly with F4/80+ macrophages. Interestingly, CD3+ T cells were present in large numbers within the adipose of both DIO and ob/ob obese mice, and flow cytometry revealed their adipose to possess significantly more CD8+ T cells than their lean cohort. CONCLUSIONS: White adipose hypoxia and cytotoxic T-cell invasion are features of obesity in C57BL/6J mice and are potential contributors to their local and generalized inflammatory state.
Subject(s)
Adipose Tissue/metabolism , Cell Hypoxia/physiology , Obesity/immunology , Adipose Tissue/pathology , Animals , CD3 Complex/immunology , CD8-Positive T-Lymphocytes/immunology , Glucose Transporter Type 1/metabolism , Hypoxia-Inducible Factor 1/metabolism , Immunohistochemistry , Macrophages/immunology , Male , Mice , Mice, Inbred C57BL , Mice, Obese , Obesity/metabolism , Obesity/physiopathology , T-Lymphocytes, Cytotoxic/physiologySubject(s)
Cyst Fluid/diagnostic imaging , Cysts/therapy , Fetal Diseases/diagnostic imaging , Fetal Diseases/therapy , Fetus , Ultrasonography, Prenatal , Adult , Chromosome Disorders/complications , Chromosomes, Human, Pair 13 , Cysts/complications , Cysts/diagnostic imaging , Delivery, Obstetric , Drainage , Female , Humans , Treatment Outcome , TrisomyABSTRACT
Neostigmine is a treatment option for colonic pseudoobstruction. However, experience in using neostigmine for this indication in pregnant women is limited. We present a case of a woman with an estimated fetal gestational age of 34 weeks presented with what was believed to be a pseudoobstruction and when conservative management failed, neostigmine was administered with no adverse side effects. Ultimately, the patient was found to have a mechanical obstruction and we discuss the challenges in making this diagnosis in pregnancy. Neostigmine may be a viable alternative to colonoscopy in pregnant women for whom mechanical obstruction is properly excluded.
Subject(s)
Colonic Pseudo-Obstruction/drug therapy , Intestinal Volvulus/diagnosis , Neostigmine/therapeutic use , Parasympathomimetics/therapeutic use , Pregnancy Complications/drug therapy , Abdominal Pain/etiology , Adult , Colectomy , Colonic Pseudo-Obstruction/diagnosis , Diagnosis, Differential , Female , Humans , Intestinal Volvulus/surgery , Pregnancy , Pregnancy Complications/diagnosis , Treatment FailureSubject(s)
Korsakoff Syndrome/blood , Korsakoff Syndrome/diagnostic imaging , Adenocarcinoma/blood , Adenocarcinoma/surgery , Endometrial Neoplasms/blood , Endometrial Neoplasms/surgery , Female , Humans , Korsakoff Syndrome/drug therapy , Middle Aged , Radiography , Thiamine/blood , Thiamine/therapeutic useABSTRACT
Both flow cytometry and fluorescence in situ hybridization (FISH) are useful techniques in the analysis of cancer tissues. When the two are used in the study of the same specimens, they are usually performed in parallel, separately. This is problematic where there is a scarcity of material, making completion of both studies impossible. Fluorescence in situ hybridization procedures that will utilize excess material discarded from flow cytometry would be advantageous. The present report describes an optimized protocol for performing sequential flow cytometry and FISH using formalin-fixed paraffin-embedded archival material. Although breast cancer tissues were used in this initial study, the protocol is applicable to other cancer tissues as well.