Promijenjeni kanonijski signalni put Hedgehog-Gli kod pesticidima inducirane aplazije koštane srži ispitan na mišjem modelu

The mechanistic interplay between pesticide exposure and development of marrow aplasia is not yet well established but there are indices that chronic pesticide exposure in some instances causes marrow aplasia like haematopoietic degenerative condition in human beings. Canonical Hedgehog (Hh) signalling has multiple roles in a wide range of developmental processes, including haematopoiesis. The present study was designed to explore the status of four important components of the canonical Hedgehog signalling cascade, the Sonic Hedgehog (Shh), Ptch1, Smo, and Gli1, in a mouse model of chronic pesticide-induced bone marrow aplasia. We used 5 % aqueous mixture of pesticides (chlorpyriphos, prophenophos, cypermethrin, alpha-methrin, and hexaconazole) for inhalation and dermal exposure of 6 hours per day and 5 days a week up to 90 days. Murine bone marrow aplasia related to chronic pesticide treatment was confi rmed primarily by haemogram, bone marrow cellularity, short term bone marrow explant culture for cellular kinetics, bone marrow smear, and fl ow cytometric Lin-Sca-1+C-kit+ extracellular receptor expression pattern. Later, components of hed ehog signalling were analysed in the bone marrow of both control and pesticide-treated aplastic groups of animals. The results depicted pancytopenic feature of peripheral blood, developmental anomaly of neutrophils, depression of primitive stem and progenitor population along with Shh, Ptch1, Smo and Gli1 expression in aplasia group. This investigation suggests that pesticide-induced downregulation of two critically important proteins - Ptch1 and Gli1 - inside the haematopoietic stem and progenitor cell population impairs haematopoietic homeostasis and regeneration mechanism in vivo concurrent with bone marrow aplasia.Mehaničko međudjelovanje izlaganja pesticidima i razvoja aplazije koštane srži još uvijek nije u potpunosti utvrđeno, ali postoje naznake da kronično izlaganje pesticidima u nekim slučajevima može uzrokovati aplaziju koštane srži poput hematopoetskoga degenerativnog stanja u ljudi. Kanonijski signalni put Hedgehog (Hh) ima višestruke uloge u mnogim razvojnim procesima, uključujući i hematopoezu. Ovo je ispitivanje imalo za cilj istražiti status četiri glavne sastavnice kanonijskoga signalnoga puta Hedgehog, Sonic Hedgehog (Shh), Ptch1, Smo i Gli1, na mišjem modelu pesticidima inducirane aplazije koštane srži. Koristili smo 5 % vodenu mješavinu pesticida (klorpirifos, profenofos, cipermetrin, alfa-metrin i heksakonazol) kojoj smo miševe izložili udisanjem i preko kože tijekom 6 sati dnevno i 5 dana tjedno do najviše 90 dana. Kronično izlaganje pesticidima vezano uz aplaziju koštane srži bilo je primarno potvrđeno krvnom slikom, celularnošću koštane srži, kratkotrajnom kulturom eksplantata koštane srži radi stanične kinetike, razmazom koštane srži i ekspresijskim obrascem protočne citometrije izvanstaničnog receptora Lin-Sca-1+C-kit+. Potom su analizirane sastavnice signalnog puta hedgehog u koštanoj srži kontrolnih jedinki i aplastičnih životinja koje su tretirane pesticidima. Rezultati su pokazali pancitopeniju periferne krvi, razvoju anomaliju neutrofi la, depresiju primitivnih matičnih stanica i prastanica uz Shh, Ptch1, Smo i Gli1 ekspresiju u skupini koja je imala aplaziju. Ovo istraživanje navodi na zaključak da pesticidi uzrokuju sniženje dvaju kritičnih proteina - Ptch1 i Gli1 - unutar hematopoetskih matičnih stanica i prastanica uzrokujući time hematopoetsku homeostazu i poremećaje regeneracijskog mehanizma in vivo zajedno s aplazijom koštane srži

Primitive Sca-1 Positive Bone Marrow HSC in Mouse Model of Aplastic Anemia: A Comparative Study through Flowcytometric Analysis and Scanning Electron Microscopy

Self-renewing Hematopoietic Stem Cells (HSCs) are responsible for reconstitution of all blood cell lineages. Sca-1 is the “stem cell antigen” marker used to identify the primitive murine HSC population, the expression of which decreases upon differentiation to other mature cell types. Sca-1+ HSCs maintain the bone marrow stem cell pool throughout the life. Aplastic anemia is a disease considered to involve primary stem cell deficiency and is characterized by severe pancytopenia and a decline in healthy blood cell generation system. Studies conducted in our laboratory revealed that the primitive Sca-1+ BM-HSCs (bone marrow hematopoietic stem cell) are significantly affected in experimental Aplastic animals pretreated with chemotherapeutic drugs (Busulfan and Cyclophosphamide) and there is increased Caspase-3 activity with consecutive high Annexin-V positivity leading to premature apoptosis in the bone marrow hematopoietic stem cell population in Aplastic condition. The Sca-1bright, that is, “more primitive” BM-HSC population was more affected than the “less primitive” BM-HSC Sca-1dim  population. The decreased cell population and the receptor expression were directly associated with an empty and deranged marrow microenvironment, which is evident from scanning electron microscopy (SEM). The above experimental evidences hint toward the manipulation of receptor expression for the benefit of cytotherapy by primitive stem cell population in Aplastic anemia cases

Alteration in Marrow Stromal Microenvironment and Apoptosis Mechanisms Involved in Aplastic Anemia: An Animal Model to Study the Possible Disease Pathology

Aplastic anemia (AA) is a heterogeneous disorder of bone marrow failure syndrome. Suggested mechanisms include a primary stem cell deficiency or defect, a secondary stem cell defect due to abnormal regulation between cell death and differentiation, or a deficient microenvironment. In this study, we have tried to investigate the alterations in hematopoietic microenvironment and underlying mechanisms involved in such alterations in an animal model of drug induced AA. We presented the results of studying long term marrow culture, marrow ultra-structure, marrow adherent and hematopoietic progenitor cell colony formation, flowcytometric analysis of marrow stem and stromal progenitor populations and apoptosis mechanism involved in aplastic anemia. The AA marrow showed impairment in cellular proliferation and maturation and failed to generate a functional stromal microenvironment even after 19 days of culture. Ultra-structural analysis showed a degenerated and deformed marrow cellular association in AA. Colony forming units (CFUs) were also severely reduced in AA. Significantly decreased marrow stem and stromal progenitor population with subsequently increased expression levels of both the extracellular and intracellular apoptosis inducer markers in the AA marrow cells essentially pointed towards the defective hematopoiesis; moreover, a deficient and apoptotic microenvironment and the microenvironmental components might have played the important role in the possible pathogenesis of AA

Suppressing Excimers in H‑Aggregates of Perylene Bisimide Folda-Dimer: Role of Dimer Conformation and Competing Assembly Pathways

Long-lived excitons in H-aggregates hold great promise for efficient transport of excitation energy, provided they are not scavenged by structurallly relaxed excimers. We report solution self-assembly of a perylene bisimide (PBI) folda-dimer that exhibits two distinct kinetic stages: an initial fast assembly leads to metastable aggregates with large excimer contribution that is followed by a slower growth of stable, extended H-aggregates free of excimers. Mechanistic investigations reveal an interplay of two competing aggregation pathways, where suppression of excimers is directly linked to the crossover from an isodesmic to cooperative aggregation. How the comeptition between two self-assembly pathways is influenced by the conformational flexibility of the folda-dimer is also discussed

Brain tumor inhibition in experimental model by restorative immunotherapy with a corpuscular antigen

805-813<span style="font-size:14.0pt;line-height: 115%;font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" mso-ansi-language:en-in;mso-fareast-language:en-in;mso-bidi-language:hi"="" lang="EN-IN">In view of the advances in our understanding of anti-tumor immune response, it is now tempting to contemplate the development of immunotherapies for malignant brain tumors, for which no effective treatment exists. Immunotherapy, with agents known as biological response modifiers (BRMs) are thus gaining increasing interest as the fourth modality of treatment. A non -specific BRM, sheep erythrocytes (SRBC) when administered (ip, 7% PCV/V, 0.5 ml) in a group of animals at the end of seventh month of ethylnitrosourea administration, resulted in significant increase in the mean survival time (&gt;350 days). Studies conducted for growth kinetics pattern with proliferation index and fluorochrome (HO - 33342) uptake techniques at the tissue culture level exhibited a regulatory inhibition of the cells isolated from tissue excised from the tumor susceptible area of brain of SRBC treated animals. Moreover, histological examination of brain from animals showed immunomodulatory role of SRBC in experimentally induced brain tumor. Further probe into the mechanisms involving immunological investigations at the cellular level in these animals indicated an augmented and potentiated cell mediated immune response (CMI) as evidenced by enhanced spontaneous rosette forming capacity and cytotoxic activity of lymphocytes and neutrophil (PMN) mediated phagocytosis respectively. The observations suggest that SRBC down regulate malignant growth pattern of experimental brain tumors either by an immunologically enhanced killing of tumor cells and/or by directly inhibiting the tumor growth possibly via a stimulated cytokine network. Thus, a corpuscular antigen, can potentiate CMI response in experimentally induced brain tumor animal model, in which response induced in the periphery are able to mediate anti-tumor effects in the brain.</span

Cooperative Self-Assembly Driven by Multiple Noncovalent Interactions: Investigating Molecular Origin and Reassessing Characterization.

International audienceCooperative interactions play a pivotal role in programmable supramolecular assembly. Emerging from a complex interplay of multiple noncovalent interactions, achieving cooperativity has largely relied on empirical knowledge. Its development as a rational design tool in molecular self-assembly requires a detailed characterization of the underlying interactions, which has hitherto been a challenge for assemblies that lack long-range order. We employ extensive one- and two-dimensional magic-angle-spinning (MAS) solid-state NMR spectroscopy to elucidate key structure-directing interactions in cooperatively bound aggregates of a perylene bisimide (PBI) chromophore. Analysis of 1H-13C cross-polarization heteronuclear correlation (CP-HETCOR) and 1H-1H double-quantum single-quantum (DQ-SQ) correlation spectra allow the identification of through-space 1H···13C and 1H···1H proximities in the assembled state and reveals the nature of molecular organization in the solid aggregates. Emergence of cooperativity from the synergistic interaction between a stronger π-stacking and a weaker interstack hydrogen-bonding is elucidated. Finally, using a combination of optical absorption, circular dichroism, and high-resolution MAS NMR spectroscopy based titration experiments, we investigate the anomalous solvent-induced disassembly of aggregates. Our results highlight the disparity between two well-established approaches of characterizing cooperativity, using thermal and good solvent-induced disassembly. The anomaly is explained by elucidating the difference between two disassembly pathways

Cytologically Diagnosed Ovarian Carcinoma Turned Out To Be a Case of Chronic Ectopic Pregnancy

Background and ndash; The diagnosis of chronic ectopic pregnancy is often difficult as there is a shortage of literature in which this disease is diagnosed as an entity separate from the condition of acute ecopic pregnancy. Experience with fine needle aspiration cytology in chronic ectopic pregnancy is not reported previously. Case - A 29-year-old para 3 woman presented with lower abdominal pain and irregular menstruation since two months Transvaginal ultrasonography showed a well defined heterogenous, solid-cystic right adnexal mass with normal serum beta HCG , and mildly elevated CA 125 level . Fine needle aspiration cytology from the mass suggested possibility of serous cyst adenocarcinoma. Abdominal hysterectomy with bilateral salpingo-oophorectomy and infra-colic omentectomy was done. Pathological findings were consistent with chronic ectopic pregnancy. Conclusion and ndash;It is possible to retrieve trophoblastic cells through fine needle aspiration even after 2 months of tubal rupture and this experience can be utilized to diagnose chronic ectopic pregnancy preoperatively. [J Interdiscipl Histopathol 2014; 2(2.000): 116-120