Which tissue does not express alkaline phosphatase (ALP)?

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Red Blood Cells Do Not Express Alkaline Phosphatase

Red blood cells do not express alkaline phosphatase, unlike placenta, liver, and bone tissues which all express this enzyme. 1, 2

Alkaline Phosphatase Distribution in Human Tissues

Alkaline phosphatase (ALP) is a group of isoenzymes found in various tissues throughout the body. The main tissues that express ALP include:

  • Placenta: Expresses placental ALP isozyme 2
  • Liver: Expresses tissue-nonspecific ALP (TNAP) isozyme 1, 3
  • Bone: Expresses tissue-nonspecific ALP (TNAP) isozyme, critical for bone mineralization 3
  • Kidney: Expresses tissue-nonspecific ALP (TNAP) isozyme 2
  • Intestinal mucosa: Expresses intestinal ALP isozyme 1, 2

Red blood cells are notably absent from this list as they do not express alkaline phosphatase. This is further supported by evidence showing that when measuring ALP in clinical settings, red blood cell preparations are not used as they do not contain this enzyme 4.

Alkaline Phosphatase Isozymes

ALP exists in four main isozymes based on tissue expression:

  1. Intestinal ALP
  2. Placental ALP
  3. Germ cell ALP
  4. Tissue-nonspecific ALP (TNAP) - found in liver, bone, and kidney 2, 3

The genetic locations of these isozymes differ:

  • Intestinal and placental ALP genes are located on the long arm of chromosome 2
  • Tissue-nonspecific ALP (liver/bone/kidney) is located on the short arm of chromosome 1 2

Functions of Alkaline Phosphatase

In tissues where ALP is expressed, it serves important physiological functions:

  • Bone: Critical for bone mineralization by hydrolyzing pyrophosphate (an inhibitor of mineralization) and increasing local inorganic phosphate concentrations 3
  • Liver: Present in the canalicular membrane of hepatocytes 1
  • Intestine: Thought to play a role in phosphate transport into intestinal epithelial cells 2
  • Placenta: Contributes to placental function

Clinical Significance

The absence of ALP in red blood cells has important clinical implications:

  • When measuring ALP levels for diagnostic purposes, hemolysis of blood samples can dilute ALP concentration and potentially lead to falsely lower values
  • In conditions where red blood cell parameters are being evaluated, ALP is not a relevant marker
  • When assessing bone or liver disorders through ALP measurements, the source of ALP is primarily from bone and liver tissues (over 80%), not from blood cells 1

In clinical practice, elevated ALP levels are typically associated with liver disorders, bone diseases, or placental issues, reflecting the tissues where this enzyme is primarily expressed 5, 6.

Measurement Considerations

When measuring ALP in clinical settings:

  • Plasma or serum samples are used, not red blood cell preparations
  • Measurement of bone-specific ALP isoenzyme can help determine the source of ALP elevation 7
  • Inflammation can affect plasma ALP measurements 4

The absence of ALP in red blood cells makes answer D (Red blood cells) the correct response to the question about which tissue does not express alkaline phosphatase.

References

Research

Alkaline Phosphatases: Biochemistry, Functions, and Measurement.

Calcified tissue international, 2023

Research

Alkaline phosphatase: an overview.

Indian journal of clinical biochemistry : IJCB, 2014

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Liver Enzyme Elevation Guideline

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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