The islets of Langerhans are microorgans located in the pancreas.
<h3>The islets of Langerhans </h3>
The islets are formed by polygonal or rounded cells, arranged in cords, around which there is an abundant network of blood capillaries with fenestrated endothelial cells.
<h3>Types of islets of Langerhans</h3>
- Alpha (A) cells: secrete glucagon. In humans, these cells have regular-shaped granules containing a dense center surrounded by a clear region under the membrane.
- Beta (B) cells: secrete insulin and amylin. B cells have irregular granules with a center formed of irregular crystals of insulin complexed with zinc.
- Delta cells (D): synthesize somatostatin.
- PP (F) cells: contain a pancreatic polypeptide.
With this information, we can conclude that the islets of Langerhans are microorgans that constitute a large production of products for the maintenance of life.
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It has been challenging to develop methods for outer-membrane(OM) isolation from <em>Leptospira</em> species and other spirochetes due to their distinctive design and a lack of sensitive cytoplasmic membrane indicators.
Spirochetes have an OM and a cytoplasmic membrane, which are divided by a periplasmic space, just like enteric gram-negative bacteria.The leptospiral OM contains a significant amount of LPS, and the leptospiral surface is dominated by its polysaccharides.
LipL32, LipL36, and LipL41 are three lipoproteins from the leptospiral OM.
Since LipL32 is an immunodominant antigen during human leptospirosis, it is recognized to be the most prominent protein in the leptospiral protein profile. OmpL1 and LipL41 together offer synergistic immunoprotection. LipL41 is a surface-exposed lipoprotein.
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I t can tell you a if something is a multicellular cell or if it isn't a multicellular cell because you might get a different discovery every time you look at a stem cell
Gigantism
and acromegaly are the two diseases resulting from hyper function of the
pituitary gland.
Gigantism
and acromegaly are conditions that are nearly always due to a pituitary adenoma
that is because of excessive secretion of a growth hormone called hypersomatotropism.
<span>If GH
hypersecretion begins in childhood, before closure of the epiphyses pituitary
gigantism occurs. It is a rare condition where skeletal growth velocity and
ultimate stature are increased, but little bony deformity occurs. However,
soft-tissue swelling occurs, and the peripheral nerves are enlarged. Hypogonadotropic
hypogonadism and deferred puberty is also normally present, resulting in a
eunuchoid habitus. While Acromegaly
occurs after the growth plate cartilage fuses in adulthood, it is the same
disorder of IGF-I excess but in acromegaly, an unadorned disease that morbidity
and mortality rates are high because its often diagnosed late, where the
disease is associated with cardiovascular, cerebrovascular, and respiratory
disorders and malignancies. </span>
Answer: idk bro
Explanation: it’s makes no sense
