Answer:
OPTION-A IS CORRECT
IT INCREASES WITH HEIGHT
Explanation:
PLEASE MARK ME BRAINLIEST
Smooth muscles depolarize as a result of a transmembrane current of Calcium ions. When an action potential depolarizes the muscle cell membrane, it also travels into the body of the cell via the t-tubules. Unlike skeletal muscle, smooth muscle is dependent in two sources of calcium in order to intiate contraction. These two sources are calcium sequestered in the S.R. of the smooth muscle cell.
Answer:
The question to be asked an investigated when observing a structure under the microscope to determine whether it is living is if it has a nucleus if eukaryote or nucleoid if prokaryote.
Explanation:
The major organelle that must be present in all living cells is the nucleus or nucleoid and the protoplasm. The observation of the cell under the microscope will show the subcellular entity, nucleus/nucleoid, more pronounced than other organelles in the cell. The nucleus house the necessary information for the maintenance and reproduction, which is mainly the genetic information that dictates the translational protein products that are needed to build another aspect of the cells. Therefore, when such a tiny structure is placed under the light microscope under the view of oil immersion, the nucleus of the cell should be visible if it is a living structure.
Answer:
Exosomes as Therapeutic Target
Given the fact that elevated exosome levels are often correlated with greater severity of different types of cancer, reducing circulating exosomes to normal levels is one of therapeutic strategies to increase treatment efficacy. There are different approaches to modulate exosome production: 1) Inhibition of exosome formation: inhibit crucial proteins involved in exosome formation pathway; 2) Inhibition of exosome release: inhibit important regulators of exosome release process, increased intracellular Ca2+, change cellular microenvironmental pH; 3) Inhibition of exosome uptake: add proteinase for surface proteins on exosomes may serve as receptors for uptake pathways. In addition to control exosomes production, removal of exosomes from the entire circulatory system might be a novel strategy for cancer treatment.
Exosomes could also be used as cancer immunotherapy becasue tumor-derived exosomes carry antigens that is a great source of specific stimulus for the immune response against tumors. Both tumor-derived and dendritic cell-derived exosomes have showed capability to stimulate tumor antigen-specific responses in experimental animal models and human clinical trials.
Exosomes as Targeted Drug Delivery Vehicles
Exosomes became one of the most common methods applied in drug delivery system because of several advantages they have. Firstly, exosomes normally have a small size 40-100 nm, which is more homogenous compared to other microvesicles. This will lead them to evade rapid clearance by the mononuclear phagocyte and enhances passage through fenestrations in the vessel wall. Secondly, due to their endogenous origin, they are less toxic for and better tolerated by the immune system. It facilitates them to avoid causing side effects that normally occur with synthetic nanoparticles. Additionally, the specific ligand or protein expressed on the exosome surface increases efficiency of cargo into the cytosol of the target cell, and therefore fewer off-target effects. Exosomes are generally found most useful as a drug delivery medium in cancer therapy, anti-inflammation and gene interference therapy such as transferring of miRNA.
There are different kinds of cargos encapsulated by exosomes, especially like siRNA or miRNA. The delivery of RNA is attracting because they are rapid degradation in cell circulation and have the limitation in passing through the membrane and in cellular uptake. Chemotherapeutics loaded into exosomes is also used for cancer therapy such as doxorubicin. In principle, there are four key components to achieve correct functionality and efficacy during exosomes drug delivery:1) Choosing the donor cell type to produce drug-carrying exosomes; 2) Using correspond methods to encapsulate the exosomes cargo; 3) Enhancing the specificity of cargo delivery by targeting peptides on the surface of the exosomes; 4) Administrating exosomes to target the area of disease.
Explanation:
https://www.creative-biostructure.com/exosome-applications-652.htm
