Myocardial Cell Types Overview

Introduction

The human heart is a highly specialized muscular organ whose efficiency depends not only on its chambers, valves, and great vessels but also on its cellular composition. The myocardium, the thick muscular layer of the heart wall, is primarily made up of cardiomyocytes, but these are not all identical. Two major cell populations exist:

  • Contractile myocytes – responsible for generating force and pumping blood
  • Specialized conduction system cells – responsible for initiating and propagating electrical impulses

Understanding these cell types, their histological features, and their distribution across atria, ventricles, and nodal tissue is fundamental to appreciating both normal cardiac physiology and the pathophysiology of rhythm disorders and heart failure.


1. Contractile Myocytes

1.1 Definition and General Features

Contractile myocytes are the workhorse cells of the heart. They:

  • Generate mechanical force
  • Contribute to the coordinated contraction of atria and ventricles
  • Account for >90% of myocardial mass

They are striated muscle cells, similar to skeletal muscle fibers but shorter, branched, and interconnected in a syncytium via intercalated discs.


1.2 Microscopic Structure

FeatureDescription
ShapeCylindrical, branched fibers (50–100 μm long, 10–20 μm wide)
NucleusSingle, centrally located nucleus (sometimes binucleate)
SarcomeresOrganized into repeating units, giving striated appearance
MitochondriaVery abundant (30–40% of cell volume) → continuous ATP supply
Intercalated DiscsContain desmosomes, fascia adherens, and gap junctions for mechanical & electrical coupling

1.3 Sarcomere Organization

The sarcomere is the fundamental contractile unit:

  • Thin filaments (actin) anchored to Z-discs
  • Thick filaments (myosin) in A-band
  • Regulatory proteins: troponin complex (T, I, C) and tropomyosin
  • Contraction is mediated by calcium binding to troponin C → conformational change → cross-bridge cycling

1.4 Functional Role

  • Responsible for atrial systole (“atrial kick”) and ventricular systole
  • Contractile force proportional to sarcomere length (Frank–Starling mechanism)
  • Excitation–contraction coupling dependent on calcium influx and calcium-induced calcium release (CICR)

2. Specialized Conduction System Cells

Specialized cardiomyocytes are not primarily contractile but are optimized for impulse generation and conduction. They include:

  1. Pacemaker cells (SA node, AV node) – spontaneously generate action potentials
  2. Conduction fibers (Bundle of His, bundle branches, Purkinje fibers) – rapidly propagate action potentials

2.1 SA Node Cells

  • Located in the sulcus terminalis at the junction of SVC and RA
  • Smaller than atrial myocytes, pale cytoplasm (fewer myofibrils)
  • Lack well-organized sarcomeres → poor contractility
  • Express HCN channels for “funny current” (If) → spontaneous diastolic depolarization
  • Primary pacemaker of the heart (60–100 bpm intrinsic firing)

2.2 AV Node Cells

  • Located in the interatrial septum, near the opening of the coronary sinus
  • Similar to SA nodal cells but slower intrinsic firing (40–60 bpm)
  • Provide physiological delay between atrial and ventricular activation (≈120 ms)
  • Critical for coordinated filling of ventricles before systole

2.3 Purkinje Fibers

  • Large diameter (≈50 μm), glycogen-rich, pale cytoplasm
  • Few contractile elements → weak contraction but extremely fast conduction (2–4 m/s)
  • Ensure synchronous activation of ventricular myocardium
  • Intrinsic pacemaker rate ≈20–40 bpm (backup in case of nodal failure)

2.4 Bundle of His and Bundle Branches

  • Located within interventricular septum
  • Intermediate conduction velocity between nodal tissue and Purkinje fibers
  • Divide into right and left bundle branches → further subdivide into Purkinje network

3. Electrophysiological Differences

FeatureContractile MyocytesPacemaker Cells
Resting Membrane Potential−85 to −90 mVUnstable (−60 mV → spontaneous depolarization)
Action Potential Phases0–4 (rapid depolarization, plateau)0 (slow upstroke), 3 (repolarization), 4 (automatic depolarization)
Ion ChannelsFast Na⁺, L-type Ca²⁺, K⁺ channelsHCN (If), T-type & L-type Ca²⁺, K⁺ channels
FunctionForce generationImpulse generation & conduction

4. Distribution Across the Heart

4.1 Atria

  • Atrial walls: mostly contractile myocytes
  • SA node and internodal pathways contain pacemaker and conduction cells
  • Atrial myocytes have less developed T-tubules, allowing rapid electrical propagation

4.2 Ventricles

  • Ventricular myocardium: dense network of contractile myocytes
  • Purkinje network runs in subendocardial layer → triggers contraction from apex upward
  • Thick myocardium requires efficient conduction for synchronized contraction

4.3 Nodal Regions

  • SA node (RA wall near SVC): pacemaker cells
  • AV node (interatrial septum): slow-conducting nodal cells, relay to His bundle
  • Together, form the “AV conduction axis”

5. Clinical Relevance

5.1 Arrhythmias

  • Damage to SA node → sinus node dysfunction (bradycardia)
  • AV nodal disease → heart block
  • Purkinje fiber dysfunction → bundle branch block, QRS widening

5.2 Myocardial Infarction

  • Ischemia kills contractile myocytes → reduces pump function
  • Purkinje network involvement → ventricular arrhythmias

5.3 Target of Drugs

  • Beta-blockers: reduce SA node automaticity and AV node conduction
  • Antiarrhythmics: block Na⁺, K⁺, Ca²⁺ channels in specific cell types

6. Histological Identification

Cell TypeKey Histological Feature
Contractile MyocyteStriated, branching fibers, central nuclei
SA/AV Node CellSmall, pale, fewer striations
Purkinje FiberVery large, pale cytoplasm, glycogen-rich
Bundle Branch FiberIntermediate size, located in septum

7. Summary Table

LocationDominant Cell TypeFunction
Atrial WallsContractile myocytesPump blood from atria to ventricles
SA NodePacemaker cellsGenerate impulse
AV NodePacemaker/relay cellsDelay conduction
His-Purkinje SystemConduction fibersRapid impulse delivery
Ventricular WallsContractile myocytesGenerate force for systemic/pulmonary circulation

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