TLS Online TPP Program

#Question id: 12698


The following test results were obtained: urine flow rate = 2.0 ml/min; urine inulin concentration = 60 mg/ml; plasma inulin concentration = 2 mg/ml; urine potassium concentration = 20 μmol/ml; plasma potassium concentration = 4.0 μmol/ml; urine osmolarity = 150 mOsm/L; and plasma osmolarity = 300 mOsm/L. What is the net potassium reabsorption rate?

#Unit 7. System Physiology – Animal
  1. 300 μmol/min
  2. 20 μmol/min
  3. 60 μmol/min
  4. 200 μmol/min
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TLS Online TPP Program

#Question id: 24204

#Unit 4. Cell Communication and Cell Signaling

What is the difference between trans and cis interactions during cell-cell adhesion respectively?

TLS Online TPP Program

#Question id: 24203

#Unit 4. Cell Communication and Cell Signaling

Heterophilic Binding appears:

TLS Online TPP Program

#Question id: 24202

#Unit 4. Cell Communication and Cell Signaling

Homophilic Binding appears:

TLS Online TPP Program

#Question id: 1388

#Unit 4. Cell Communication and Cell Signaling

When Lucifer yellow, a small dye, is injected into a neuron of the retina, neighboring neurons become rapidly labeled. If the retina is incubated in dopamine prior to Lucifer yellow injection, only the injected neuron becomes labeled. These findings suggest which of the following?

I. Neurons of the retina communicate via gap junctions.

II. Dopamine is transferred between cells via gap junctions.

III. Dopamine decreases the permeability of gap junctions.

TLS Online TPP Program

#Question id: 1387

#Unit 4. Cell Communication and Cell Signaling

The ability of a population of fibroblasts to migrate along the surface of a tissue culture dish depends on adhesion between the cell surface and the extracellular matrix molecules coating the dish. The dish is coated with laminin, and the only cell-surface protein capable of binding laminin is a cell-adhesion protein called an integrin. Integrins are integral plasma-membrane proteins that function as heterodimers. Under these conditions the rate at which a fibroblast can migrate along the laminin coated culture dish is proportional to the strength of adhesion between the cell and the laminin substrate. The table below lists the rate of cell migration observed for fibroblasts genetically engineered to generate the indicated phenotypes. Microinjection into the cytoplasm of a wild. type cell of a solution of a synthetic peptide possessing the same sequence as the integrin beta subunit cytoplasmic domain would be expected to yield an average fibroblast-cell migration rat

Fibroblast Phenotype

Level of Integrin Heterodimer at the Cell Surface (percent of wild type)

Rate of Cell Migration (pm/min) 

1. Wild type

100

2

2. Overexpression of the wild-type integrin alpha subunit

104

2

3. Overexpression of an integrin beta subunit lacking the cytoplasmic domain

96

0.6

4. Overexpression of the soluble cytoplasmic domain of an integrin beta subunit

98

0.6

5. Absence of the integrin alpha subunit

Less than 1

0.05

TLS Online TPP Program

#Question id: 1386

#Unit 4. Cell Communication and Cell Signaling

The ability of a population of fibroblasts to migrate along the surface of a tissue culture dish depends on adhesion between the cell surface and the extracellular matrix molecules coating the dish. The dish is coated with laminin, and the only cell-surface protein capable of binding laminin is a cell-adhesion protein called an integrin. Integrins are integral plasma-membrane proteins that function as heterodimers. Under these conditions the rate at which a fibroblast can migrate along the laminin coated culture dish is proportional to the strength of adhesion between the cell and the laminin substrate. The table below lists the rate of cell migration observed for fibroblasts genetically engineered to generate the indicated phenotypes. One explanation for the effect of overexpression of the cytoplasmic domain of the integrin beta subunit is that this domain normally functions to bind a cytoplasmic factor necessary for integrin function. Which of the following would be the most informative experiment to identify the cytoplasmic factor?